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A government contract requires that this position be restricted to U.S. citizens or legal permanent residents. You must provide documentation that you are a U.S. citizen or legal permanent resident to qualify. \n This position requires an active Secret clearance or the ability to obtain a Secret clearance to be considered. \n Position Summary: \n The CERCLA/RCRA Engineering Support (ES) II position supports the Navy’s Base Realignment and Closure (BRAC) Program Management Office (PMO). The ESII provides technical and program support to BRAC PMO management, BRAC Environmental Coordinators (BECs), and Lead Remedial Project Managers (LRPMs) overseeing the investigation and cleanup of Navy BRAC properties under the Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA) and Resource Conservation and Recovery Act (RCRA). The RPM is expected to demonstrate technical proficiency to advance assigned projects through the CERCLA and RCRA process toward site closure or long-term management. This is a non-personal services position; the successful candidate will be adept at working closely with Navy cleanup contractors and regulatory agencies, developing high-quality technical deliverables, performing rigorous data analysis, and preparing draft documentation that supports government decision-makers. \n \n Compensation & Benefits: \n Starting Salary Range for CERCLA/RCRA Engineering Support II (Remedial Project Manager support): $110,000 – $115,000 \n Benefits That Set Us Apart \n When considering your next opportunity, compensation is only part of the picture. We offer a benefits package designed to invest in your future and support your life outside of work. \n Highlights include: \n • Up to a 6% 401(k) company match to help you build long-term financial security \n • Paid time off as part of our comprehensive benefits package, so you have the flexibility to rest, recharge, and enjoy what matters most \n • Medical, dental, and vision insurance, plus prescription drug coverage \n • Basic life and AD&D insurance, with supplemental life options \n • Short-term and long-term disability coverage \n • Paid holidays \n • Employee Assistance Program (EAP) \n • Flexible Spending Account (FSA) and Health Savings Account (HSA) options \n • Professional development, training, and certification support \n • Voluntary benefits including accident, critical illness, and identity theft protection \n Because taking care of our employees isn’t just a promise, it’s part of who we are. \n Benefits are subject to change and eligibility requirements apply. \n \n Essential Functions, Duties & Responsibilities: \n Includes the following: \n • Provide project management support for assigned Navy BRAC sites, successfully advancing projects through the CERCLA and RCRA process toward site closure or long-term management, as appropriate. \n • Perform project management tasks including data collection, regulatory agency interface, developing cost estimates, preparing statements of work (SOW), and drafting correspondence according to established milestones, with reviews for quality and progress to assure schedules, cost estimates, and strategies are accurate and executable. \n • Work closely with Navy environmental contractors conducting CERCLA/RCRA investigation and cleanup work at BRAC sites to ensure they are adhering to project scopes and schedules; identify issues and recommend corrective actions to the LRPM. \n • Support work executed under a variety of contract types such as Firm-Fixed-Price, Indefinite Delivery/Indefinite Quantity (IDIQ), Multiple Award Contracts (MACs), Remedial Action Contracts (RACs), and CLEAN contracts. \n • Review Environmental Restoration (ER) Program CERCLA documents, such as Remedial Investigations/Feasibility Studies (RI/FS), Proposed Plans, Records of Decision, Remedial Designs (RD), and Remedial Action Completion Reports, to determine whether the requirements of CERCLA, the National Oil and Hazardous Substances Contingency Plan (NCP), RCRA, and other Applicable or Relevant and Appropriate Requirements (ARARs) are being met. \n • Research and interpret federal and state environmental laws and regulations (proposed and existing) and determine their applicability to specific projects conducted under the ER Program, including CERCLA, the Superfund Amendments and Reauthorization Act (SARA), RCRA, state hazardous waste laws, the Clean Air Act, and the Clean Water Act. \n • Suggest innovative technical principles, practices, theories, and resolutions to technical issues to BRAC PMO management, BECs, and/or LRPMs. \n • Perform regular and recurring field activities, including field inspections, investigations, and surveys at remediation sites. \n • Brief BRAC PMO management, BECs, and/or LRPMs on project status, and assist BECs and/or LRPMs in preparing briefings for Base Closure Managers (BCMs) and BRAC management. \n • Conduct internal and external presentations on the status of assigned projects. \n • Participate in subject matter meetings, including project meetings with contractors, meetings with regulatory agency representatives, internal staff meetings, and organizational meetings; prepare attendance notes and track action items. \n • Interact on a daily basis with personnel from multiple regulatory agencies, including the U.S. Environmental Protection Agency (EPA), U.S. Fish and Wildlife Service, and state and local regulatory agencies. \n • Performs other job-related duties as assigned within the scope of the contract. \n • No supervisory/management authority. \n • Remedial Project Manager Experience, Education, Skills, Abilities requested: \n \n Supervisory Responsibilities: \n No supervisory/management authority \n \n Basic Qualifications: \n\n • Bachelor’s degree in the physical sciences, including Environmental Science, Geology, Chemistry, Biology, or Engineering, from an accredited college or university.\n\n, • Minimum of six (6) years of experience, including at least three (3) years working on CERCLA and/or RCRA projects or other related federal environmental projects. \n • Knowledge of a wide range of concepts, principles, and practices as applied to CERCLA/RCRA engineering. \n • Knowledge of the laws, regulations, and standards applicable to the specialty, including federal and state regulations relevant to the investigation and remediation of CERCLA hazardous substances, munitions, radiological materials, lead-based paint, asbestos, and petroleum, including but not limited to CERCLA, SARA, RCRA, state hazardous waste laws and regulations, the Clean Air Act, and the Clean Water Act. \n • Experience in broad-based CERCLA/RCRA topics, including investigation and remediation of various media such as soil, sediment, groundwater, and soil gas. \n • Current U.S. Occupational Safety & Health Administration (OSHA) Hazardous Waste Operations and Emergency Response Standard (HAZWOPER) certification and appropriate refresher. \n • Proficient using Microsoft Office Suite (Excel, Word, PowerPoint, Project, and Outlook). \n • Ability to perform regular and recurring field inspections, investigations, or surveys in which there is a considerable amount of walking, stooping, bending, and climbing. \n • Ability to perform work in an office setting, with occasional visits to remediation sites. \n • Work involves moderate risks of discomfort that require adherence to safety precautions. \n • Valid REAL ID driver’s license. \n • Ability to obtain and maintain a favorable Tier 3 background investigation supporting limited privilege and sensitive (non-classified) information access, and to obtain a Common Access Card (CAC). \n • Ability to successfully pass a drug screen and background check. \n • Past applicable job experience may include, but is not limited to: Remedial Project Manager, Environmental Restoration Project Manager, Environmental Project Manager, Senior Environmental Engineer, or Environmental Engineer III. \n • Perform other job-related duties as assigned. \n • Must be a US Citizen. \n • This position requires a Common Access Card (CAC), the ability to pass the U.S. Department of Defense (DoD) clearance to acquire a Common Access Card (CAC). \n • This position requires an active Secret clearance or the ability to obtain a Secret clearance to be considered. \n • Prolonged periods of sitting at a desk and working on a computer; may occasionally require standing or moving about the office for extended periods. \n • Must pass pre-employment qualifications of Cherokee Federal. \n \n Preferred Qualifications: \n • Preferred: Prior experience supporting a Navy or other DoD environmental restoration program as a Remedial Project Manager or in an RPM-support role; Navy BRAC or NAVFAC experience; Master’s degree, Professional Engineer (PE), Professional Geologist (PG), or Project Management Professional (PMP) credential. \n \n Work Environment: \n Work is performed primarily in a climate-controlled environment. \n \n Company Information: \n Behind every government mission stands skilled, mission-driven talent: people whose expertise and dedication turn complex challenges into successful outcomes. Cherokee Nation Government Solutions, part of Cherokee Federal, the federal contracting division of Cherokee Nation Businesses, is that team. We modernize aging systems, deliver care where it’s needed most, and keep missions supplied, staffed, and moving across defense, intelligence, and civilian agencies. For more than 60 federal clients, we take on the work others won’t, and deliver where it counts. If that’s the kind of work you’re looking for, you’ve found your team. Learn more at cherokee-federal.com. \n \n \n Cherokee Federal is a military friendly employer. Veterans and active military transitioning to civilian status are encouraged to apply. \n Legal Disclaimer: All qualified applicants will receive consideration for employment without regard to protected veteran status, disability or any other status protected under applicable federal, state or local law. \n Many of our job openings require access to government buildings or military installations. Candidates must pass pre-employment qualifications of Cherokee Federal. \n Pursuant to California SB 1162, the estimated annual salary range for this position is $110,000 – $115,000. Actual compensation may vary based on experience, skills, and qualifications. \n \n Equal Employment Opportunity (EEO) Statement \n Cherokee Federal is a federal contractor subject to the Vietnam Era Veterans’ Readjustment Assistance Act (VEVRAA). As required by VEVRAA, we take affirmative action to employ and advance in employment qualified protected veterans. Protected veterans are encouraged to self-identify during the application process. \n Cherokee Federal takes affirmative action to employ and advance in employment qualified individuals with disabilities in compliance with Section 503 of the Rehabilitation Act. Qualified individuals with disabilities are encouraged to self-identify during the application process. \n Reasonable accommodations are available to qualified individuals with disabilities or those with sincerely held religious beliefs. To request an accommodation in the application or interview process, please contact Human Resources at careers@cherokee-federal.com.

Job Summary \n\n • Responsible for research and development and activities associated with oligos. Provides oligo process support to Operations group through instrument/oligo process troubleshooting and completion of NCR investigations. Support operations as needed with the manufacture of GMP oligonucleotides; the continuous improvement of these existing oligo processes; and the development/transfer of new oligo processes.\n\n \n Essential Duties and Responsibilities \n\n • Independently produces notebook, dev, pilot and production materials per written directions\n, • Assist Core Team and Extended Core Team Members with New Product Development\n, • Assist team members with NCR investigations and associated testing\n, • Analyzes in-process and final oligos using state-of-the-art analytical techniques\n, • Troubleshoots simple manufacturing process problems\n, • Analyze, track, and trend New Product Development associated process data\n, • Creates documents and assists with assembly of change control packages\n, • Maintains labs under cGMP conditions\n, • Completes ERP and cycle count transactions\n, • Keeps accurate records and documentation\n, • Stocks and maintains lab supplies\n\n \n Required Qualifications: \n • Bachelor’s degree in Biology, Chemistry, or another science-related field \n • Knowledge of Good Manufacturing Practices and Good Documentation Practices \n • Strong attention to detail \n • Positive work ethic and ability to work effectively in a team environment \n • This is an entry-level opportunity. Candidates should have no more than approximately five years of related experience. \n \n Preferred Experience: \n • Oligonucleotide synthesis \n • Oligonucleotide purification using HPLC \n \n Physical and site requirements: \n • Must be able to lift up to 50 pounds occasionally \n • Personal protective equipment is required while working in the laboratory \n • Business-casual attire and closed-toe shoes are required \n

Job DescriptionPatent Litigation Associate Attorney (Life Sciences/ANDA) Locations: Washington, DC, San Diego & Palo Alto, CA Practice Area: IP Litigation (Life Sciences) Direct Counsel is seeking an IP Litigation Associate to join a leading firm’s Washington, DC or Palo Alto office. This role is ideal for candidates with ANDA and/or life sciences patent litigation experience who are eager to take on substantive responsibilities, including courtroom advocacy and depositions. Key Responsibilities: • Handle patent litigation matters in U.S. District Courts and before the PTAB., • Conduct factual and legal research, draft pleadings, and develop case strategies., • Participate in discovery on infringement, validity, and damages issues., • Take and defend depositions, draft dispositive motions, and handle claim construction briefing., • Engage in pre-trial and trial activities., • Work directly with clients, opposing counsel, and internal teams.Qualifications:, • 2-6 years of patent litigation experience at a comparable law firm., • Experience in Hatch-Waxman (ANDA) litigation or other life sciences patent matters., • Undergraduate or master’s degree in biology, chemistry, biochemistry, or related life sciences discipline (preferred)., • Strong oral advocacy skills with courtroom and deposition experience., • JD from a top-tier law school with strong academic credentials., • Excellent legal research, writing, and analytical skills.Compensation & Benefits:, • Salary Range: $235,000 - $365,000 (Final offer based on experience and location)., • Comprehensive benefits, including medical, dental, vision, and firm-paid life insurance., • Generous vacation, sick leave, and parental leave., • Professional development and mentorship opportunities. This is an exciting opportunity for a mid-level IP litigator to join a top-tier team with a cutting-edge life sciences practice. Apply today to learn more!

Job Description Genomic Life is seeking a talented and enthusiastic Patient Navigator to join our team. The Patient Navigator is an individual contributor responsible for facilitating and coordinating personalized navigation services for Genomic Life Members. Working under the Clinical Supervisor, this person will provide initial triage for Genomic Life services, ensure accurate documentation of patient data, and connect patients with appropriate resources to meet their practical, social, physical, emotional, and spiritual needs. The Patient Navigator works in collaboration with Clinical Navigators and the multidisciplinary team, demonstrating active listening skills, empathy, and a strong understanding of evidence-based genomic information. Job Type: Full time Hours: M-F 8-5 pm Location: Remote or Hybrid in San Diego, CA Salary Range: $50-70k Responsibilities • Provide initial triage for Genomic Life services by identifying members' navigation needs related to genetic testing, cancer diagnosis, or caregiver support, • Act as the primary point of contact for members seeking assistance with accessing benefits, promptly addressing inquiries, and resolving any issues they encounter, • Handle member concerns and complaints with professionalism and empathy, actively listening to their feedback and working towards mutually beneficial resolutions, • Demonstrated ability to effectively prioritize tasks and maintain impeccable organization in a fast-paced environment, ensuring deadlines are met and objectives are achieved efficiently, • Initiate personalized navigation services based on patient and program requirements, • Engage in ongoing professional development to maintain a current working knowledge of evidence-based healthcare and genomic information and support quality-of-care coordination, • Ensure accurate triage documentation and verification of all required patient data using pre-designated tools, • Participate in tracking and monitoring metrics and outcomes, collaborating with administration, and reporting findings to relevant stakeholders, • Communicate patient information appropriately to the Genomic Life Clinical Services team and within the healthcare team, • Identify potential and existing barriers to care and facilitate access to appropriate, credible resources tailored to members' individual needs, including reading level, health literacy, culture, language, and preferred level of information, • Promote prevention behaviors, early detection, screening, and healthy behavior education among members, • Schedule member appointments for Clinical Navigator and Genetic Counseling as appropriate, • Request and track medical records to facilitate seamless care, • Utilize active listening skills and remain solution-oriented when interacting with patients, families, and members of the healthcare team, • Demonstrate empathy, integrity, honesty, and compassion when engaging in conversations with members, • Demonstrate cultural humility, sensitivity, and responsiveness to diverse patient populations, including gender/gender identity, age, culture, race, ethnicity, religion, abilities, and sexual orientation, • Participate in collaborative team communication and escalate operational challenges to Clinical Navigation leadership to support effective problem-solving and optimize service delivery, • Adhere to all HIPAA guidelines for privacy and confidentiality practices, • Demonstrate knowledge of and adherence to GINA requirements and organizational practices related to the appropriate use, handling, and protection of genetic information Requirements • Bachelor's degree in public health, biology, or other related field, OR Associate of Science degree with 5 or more years of healthcare-related experience, • Experience as a Patient Navigator or similar role within healthcare, preferred, • Navigation Training (GW Patient Navigation Training or ACS LION Patient Navigation Training) is preferred, • Knowledge of evidence-based healthcare and patient navigation principles, • Strong communication skills, both verbal and written, • Ability to work collaboratively in a multidisciplinary healthcare team, • Strong interpersonal skills with sensitivity to cultural diversity and the ability to navigate diverse patient populations, • Demonstrates initiative, critical thinking, and is a self-starter, • Detail-oriented, highly organized, able to manage time and competing priorities, • Strong technology skills and quickly learns new technologies; Proficient in Microsoft Office and Zoom, and able to learn new software (Salesforce.com) Genomic Life is an Equal Opportunity Employer. About Genomic Life: Genomic Life's mission is to be the best in the world at navigating individuals to the genomics that matter. We provide clinically relevant proactive genetic testing all in one program, making it easy to prevent, diagnose, and treat disease. Our nationwide team is driven to make a difference for the members, clients, and patients we serve. We are bringing the science of today to the medicine of tomorrow. We are passionate about what we do and the extraordinary transformation that genomics will have on healthcare.

Job Description We are seeking a Care Manager - CA to join our team at Independent Living Systems (ILS). ILS, along with its affiliated health plans known as Florida Community Care and Florida Complete Care, is committed to promoting a higher quality of life and maximizing independence for all vulnerable populations. About the Role: The Care Manager in California plays a pivotal role in coordinating and managing comprehensive care plans for individuals requiring health and social support services. This position ensures that members receive personalized, effective, and timely care by collaborating with healthcare providers, social workers, and family members. The Care Manager acts as a liaison to facilitate communication among all parties involved, advocating for the client’s needs and preferences. They monitor client progress, adjust care plans as necessary, and ensure compliance with regulatory standards and organizational policies. Ultimately, the role aims to improve client outcomes, enhance quality of life, and optimize resource utilization within the care continuum. Minimum Qualifications: • Bachelor’s degree in social work, Psychology, Biology, Public Health, Nursing, Community Health, or Health related field or equivalent experience required., • Requires at least 5 years of experience working with people who need assistance with complex health and social issues., • Requires knowledge of and experience working with community agencies and programs., • Requires experience with Medi-Cal eligibility guidelines, application, and renewal/redetermination process., • Requires strong problem-solving and customer service skills., • Must be a CA Resident and must reside in CA while employed., • Current and valid California (CA) Driver’s License., • Must use personal vehicle and current vehicle registration required., • Proof of auto insurance required, must maintain CA minimum insurance coverage., • BCLS CPR Certification required. Preferred Qualifications: • Master’s degree in Nursing, Social Work, Public Health, or Healthcare Administration., • Certified Case Manager (CCM) credential or equivalent certification., • Experience working with diverse populations including elderly, disabled, or chronically ill clients., • Bilingual abilities, particularly in Spanish or other commonly spoken languages in California. Responsibilities: • Develop and manage Individualized Care Plans for members in assigned caseload and provide consistent and effective care coordination as indicated by the Care Plan., • Assess psychosocial and social determinants of health needs for high-risk members and document assessment results or augment available information in appropriate systems, • Consult with or refer members to licensed staff (social worker, nurse case manager etc.) as required based on member social, health risk and medical complexity., • Establish relationships and partner with community resources, health plans and providers by participating in community engagement activities with local agencies e.g. faith-based organizations, community centers, government agencies, parks, recreation centers and schools, • Assist members with problem solving barriers to high complexity health conditions by identifying, locating, connecting to and navigating needed community and medical system services, including visiting members at their homes, accompanying members to medical appointments and assisting members with completing forms to access needed services, • Actively engage, build rapport, establish trusting relationships and facilitate collaborative communication with members and member family support systems, • Identifies social determinants of health concerns/ gaps, develops and documents a plan to address complex social and health disparities, • Documents member updates and progress notes in appropriate systems, submits timely reports, and provides recommendations for improved member outcomes tracking, • Identifies gaps in community resources and medical systems, makes recommendations to close gaps and implements new services or solutions to close identified gaps

Job Description JOB DESCRIPTION Job Summary: Reporting to the Microbiology Lab Supervisor, the Sr. QC Technician is responsible for supporting activities within the Microbiology Lab. The role performs studies and microbiology testing required by established work instructions, procedures, protocols, and standards. The technician must exercise accuracy and attention to detail, maintain accurate records, and ensure compliance with internal Quality Assurance procedures and external standards and regulations. Job Responsibilities: (Primary Duties, Roles, and/or Authorities) • Responsible for sterility testing (SDAs and BI, if applicable), non-sterile bioburden testing and particulate testing while maintaining a sterile field., • Responsible for LAL testing and associated validations/revalidations., • Responsible for supporting training and testing and ensuring turnaround times are met., • Environmental monitoring of the laboratory, controlled areas, and lab spaces as applicable., • Preparing media for testing, quality checks, and sterilization of testing equipment., • Metrics, gathering and trending of test data., • Review QMS documents and procedures prior to release or update as required., • Proactively identify compliance issues and verify alignment with internal and external standards and policies. • Notify and work closely with functional management when OOS occurs., • Maintain a positive and cooperative team dynamic., • May assist in the design and implementation of new laboratory equipment., • Other duties as assigned., • Support training initiatives and training of new associates Education and Experience: 1. Typically requires a minimum of a Bachelor's degree in science (Microbiology or Biology related) with 5 years relevant experience in a related discipline. 1. Understanding of ISO 13485, 21 CFR 820 and other related standards.

Job Description Location: San Diego, CA Job Type: Full-Time Salary: $175,000 - $190,000 Position Overview We are seeking a Senior Staff Scientist to provide technical leadership for assay development under design control, with primary responsibility for analytical verification and validation of laboratory-developed tests (LDTs). This role will set validation strategy, translate product and clinical requirements into rigorous study plans and acceptance criteria, and ensure high-quality execution and documentation in a regulated environment. The successful candidate will combine strategic scientific leadership with a willingness to perform hands-on laboratory work. The role partners closely with R&D, Product Management, Clinical, Lab Operations, Bioinformatics, Software, Quality, and Regulatory throughout the product development lifecycle, from design inputs through launch and post-launch improvements. Key Responsibilities • Own or co-own design verification and analytical validation strategy for assigned assays, including study design, sample and replicate plans, acceptance criteria, statistical approach, execution, data interpretation, and final reports., • Design and lead analytical performance studies, as applicable, including accuracy, precision and reproducibility, analytical sensitivity and specificity, limit of detection, linearity or reportable range, interference, carryover, contamination risk, stability, robustness, and method or instrument equivalency., • Partner with Product Management, Clinical, and Regulatory to translate intended use, product requirements, and clinical needs into clear, testable design inputs and verification or validation methods., • Maintain traceability among user needs, design inputs, design outputs, risk controls, test methods, protocols, results, and design changes., • Perform and/or directly supervise hands-on laboratory work for critical experiments, method troubleshooting, and analytical validation studies., • Author and review high-quality development and quality documentation, including study plans, protocols, reports, SOPs, work instructions, technical assessments, deviations, investigations, and change-control records., • Communicate technical risks, tradeoffs, recommendations, and decisions clearly to cross-functional stakeholders and company leadership., • Mentor junior scientists and establish high standards for experimental design, data integrity, documentation quality, and scientific communication. Qualifications Required: • Degree in Molecular Biology, Biochemistry, Biotechnology, or related discipline., • PhD with 10+ years of relevant industry experience or BS/MS with 15+ years of relevant industry experience., • Demonstrated experience advancing LDT products from development through analytical validation, transfer, and launch., • Substantial hands-on experience designing, executing, analyzing, and documenting analytical verification and validation studies for LDTs., • Strong working knowledge of design controls, risk management, cGMP principles, and ISO 13485-aligned quality systems., • Experience working in a regulated clinical laboratory and/or diagnostic product-development environment, such as CLIA, CAP, or New York State-regulated laboratories., • Proven ability to generate and critically review high-quality technical and quality documentation suitable for audits, inspections, and regulatory review., • Demonstrated ability to lead complex cross-functional initiatives and influence scientific, engineering, operational, quality, and regulatory stakeholders without direct authority., • Strong scientific judgment, structured problem-solving skills, and clear written and verbal communication., • Willingness and ability to perform hands-on laboratory work as program needs require., • Demonstrated commitment to mentoring and developing scientists. Preferred: • Experience with high-complexity NGS assays., • Experience supporting regulatory interactions, submissions, or reimbursement evidence packages, including MolDX, in partnership with Quality and Regulatory., • Experience with automated or high-throughput assay workflows and transfer into regulated clinical laboratory operations., • Familiarity with CLSI guidance and statistical methods used in analytical performance evaluation. We are an equal opportunity employer. We thrive on diversity and collaboration.

Job Description Title: Scientific Technician Location: San Diego, CA:92121 Contract: 05+ Months Job Description: The Technician II (Purification) is responsible for purifying custom oligonucleotides according to the customer’s order. This generally includes the sorting, purification, and QC sampling of the products being made. In this role, you will have the opportunity to: • Synthesize custom oligonucleotides, • Purify oligos using ion-exchange and reverse phase methods, • Measure quality using optical density, mass spectrometry, and capillary electrophoresis The essential requirements of the job include: • Adheres to safety regulations, lab SOPs, and contamination controls, • Synthesizes custom oligonucleotides on various platforms, • Performs the purification of oligos using various techniques, • Uses automated and manual lab equipment including limited maintenance and troubleshooting activities, • Quantifies and samples oligos for quality control tests, • Assesses QC data accurately and assigns pass/fail dispositions for oligos, • Ensures that product meets final purity guarantees through the custom purification process, • Sorts oligos for the proper purification method using software, • Troubleshoots oligo failures and makes thoughtful sorting and purification decisions, • Follows and records process steps accurately, • Demonstrates behavior consistent with the Integrated DNA Technologies Core Values, • Performs other duties as assigned Education: • Associate’s (2 year) degree or comparable combination of education and experience required, • Bachelor’s (4 year) degree in a science related field (Biology, Chemistry, etc.) preferred Experience: • Proficiency in a variety of PC software programs with strong working knowledge of Microsoft Office required Other Job Qualifications • Ability to work in a team environment, remaining attentive to ideas, recognizing responsibilities, and actively participating with others to accomplish assignments and achieve desired goals, • Strong attention to detail, • Ability to communicate with peers and all levels of management, • Ability to manage time and work independently, • Ability to prioritize and organize workload to efficiently accomplish departmental goals, • Uses aids and SOPs to make decisions about the proper production path per product, • Ability to perform under stress when confronted with emergent, critical, unusual, or dangerous situations, • Ability to perform a variety of duties, without loss of efficiency or composure, • Ability to maintain both a high standard of courtesy and cooperation in dealing with co-workers, • Ability to accept responsibility for the direction, control, or planning of an activity, • Adaptability to situations requiring the precise attainment of set limits, tolerances, or standards, • Ability to perform repetitive work regularly, including capping and labeling test tubes Physical Requirements: Exert 20-50 lbs. of force occasionally and/or 10-15 lbs. of force frequently Constant (67%-100% of work day) • Reaching: extending hand(s) and arm(s) in any direction., • Using Fingers/Grasping/Feeling: writing or otherwise working, primarily with fingers rather than with the whole hand or arm as in handling. Applying pressure to an object with the fingers or palm and perceiving attributes of objects such as size, shape, temperature, or texture by touch., • Talking: expressing or exchanging ideas by means of the spoken work - those activities in which they must convey detailed or important spoken instructions to other workers accurately, loudly, or quickly., • Hearing: perceiving the nature of sounds at normal range; ability to receive detailed information through oral communication, and to make fine discriminations in sound, such as when auscultating and percussing., • Repetitive Motion: substantial movements (motion) of the wrists, hands, and/or fingers. Frequently (34-66% of work day) • Sitting: to assume a position in which the weight is largely supported by the buttocks, usually with the body vertical and the thighs horizontal., • Standing: maintaining an upright position., • Walking: moving about on foot to accomplish tasks., • Lifting: raising objects from a lower to a higher position or moving objects horizontally from position to position., • Bending: bending body downward and forward by bending spine at the waist and/or bending leg; bending legs at knee to come to rest or kneel., • Pushing/Pulling: using upper extremities to press against something with steady force to thrust forward, downward or outward/using upper extremities to exert force to drag, haul or tug objects in a sustained motion. Occasional (33% or less of work day) • Climbing: stairs, stools, ramps, ladders. Visual Acuity: • Work requires close vision, distance vision, peripheral vision, depth perception and ability to adjust focus, • Ability to read pertinent printed material and distinguish colors, • Ability to accurately read measurements on equipment, • Ability to prepare and read written documentation, using a computer It would be a plus if you also possess previous experience in: • Manufacturing, • Purification, • Quality Control\nCompany Description LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch. LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.

Job Description We are seeking a Housing Navigator to join our team at Independent Living Systems (ILS). ILS, along with its affiliated health plans known as Florida Community Care and Florida Complete Care, is committed to promoting a higher quality of life and maximizing independence for all vulnerable populations. About the Role: The Housing Navigator plays a critical role in connecting individuals and families experiencing housing instability with appropriate housing resources and support services within the healthcare sector. This position focuses on assessing client needs, identifying suitable housing options, and facilitating access to community resources to promote long-term housing stability and improved health outcomes. The Housing Navigator collaborates closely with healthcare providers, social service agencies, and landlords to coordinate care and ensure seamless transitions into safe and affordable housing. By providing personalized guidance and advocacy, the Housing Navigator helps reduce barriers to housing and supports clients in maintaining their housing arrangements. Ultimately, this role contributes to enhancing the overall well-being and quality of life for vulnerable populations through effective housing solutions integrated with healthcare services. Minimum Qualifications: • Bachelor’s degree in social work, Psychology, Biology, Public Health, Nursing, Community Health, or Health related field or equivalent experience required., • Requires at least 5 years of experience working with people who need assistance with complex health and social issues., • Requires knowledge of and experience working with community agencies and programs., • Requires experience with Medi-Cal eligibility guidelines, application, and renewal/redetermination process., • Requires strong problem solving and customer service skills., • Must have a strong understanding of the DHCS housing and tenancy program and services and requirements., • Must demonstrate proficiency in or willingness to learn HMIS and other data entry systems., • Must be a CA Resident, and must reside in CA while employed., • Current and valid California (CA) Driver’s License., • Must use personal vehicle and current vehicle registration required., • Proof of auto insurance required, must maintain CA minimum insurance coverage., • BCLS CPR Certification required. Preferred Qualifications: • Certification in case management or housing navigation., • Experience working within healthcare settings or with interdisciplinary care teams., • Familiarity with electronic health records (EHR) and case management software., • Bilingual abilities or proficiency in additional languages relevant to the community served., • Training in trauma-informed care and cultural competency. Responsibilities: • Conduct comprehensive assessments of clients’ housing needs and barriers to stable housing and collaborates to develop Individualized Service Plan (ISP) that addresses housing goals, maintaining/increasing income and other personal goals identified by the participant including medical, mental health, substance use, financial resources, vocational, and social support needs, • Provides referrals, linkages, information, and support to resources that help participants to achieve their ISP goals, • Completes program specific assessments., • Evaluates strengths and challenges to addressing short term and long-term goals, conducts a 90-day review with the participant after initial intake., • Develop individualized housing plans in collaboration with clients and multidisciplinary teams., • Identify and maintain up-to-date knowledge of available housing resources, subsidies, and community programs., • Advocate on behalf of clients with landlords, housing authorities, and service providers to secure housing placements. Also must focus on landlord engagement and retention that involves negotiation and advocacy., • Provide ongoing support and follow-up to ensure housing stability and address any emerging challenges., • Coordinate with healthcare providers to integrate housing solutions with clients’ health and social care plans., • Maintain accurate documentation of client interactions, housing plans, and outcomes in compliance with organizational policies., • Participate in community outreach and education efforts to raise awareness of housing resources and services.

Job Description 2025 was a Record Sales Year. And 2026 is trending to be even Better. A new opening: Technical Sales Territory Manager for a San Diego California based territory. Sell boiler and cooling tower industrial water treatment chemicals with unlimited commission potential. Work out of your home anywhere in San Diego county. Garratt-Callahan is a profitable and private nationwide water treatment chemical company that promotes from within. We are one of the largest private water treatment companies in the U.S. We are stable, and well respected in our industry. G-C is expanding nationwide in 2026 and we are looking for aggressive, smart, educated, and promotable Technical Sales Territory Managers to join our sales team. We offer training, technical support, and an unlimited no-cap flat rate commission. Sell water treatment boiler and cooling tower chemicals to a variety of industrial customers. Maintain the existing customer base and make cold calls to develop new business. Work alongside friendly, veteran salespeople. This is an established territory with a sizeable book of business. It includes customers in Healthcare, Food & Beverage, Pharmaceutical, Manufacturing, Government, Commercial & Institutional, and Wastewater. Run chemical tests to analyze water and document results. Interact and fix mechanical equipment such as pumps, tubing, piping and valves. Program electronic equipment such as cooling tower chemical controllers. Military and mechanical backgrounds are helpful. Garratt-Callahan is proud to offer: • Compensation is based upon experience and the ability to succeed., • $90,000 to $130,000+ first year for a qualified candidate., • Great benefits including a corporate 401k, health, dental, vision, and life insurance., • Industry competitive no cap flat rate commission. And we have not changed our commission plan in 25 years. Our top Territory Sales Managers make six figure commissions. Yes, you read that right. Unlimited commission, no cap., • Expenses, and a Car Allowance of $675 per month., • Technical Support and Ongoing Training., • Stability and peace of mind. No layoffs in our 120-year history. Debt free, profitable, and growing. To Apply, please log on to: https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=16ed56fa-3af7-47fc-878a-c4d47df49e2f&ccId=19000101000001&jobId=571885&source=CC2&lang=enUS Garratt-Callahan is an EEO/AAE employer. Minorities, women, veterans, and individuals with disabilities are encouraged to apply. You may live anywhere in or near San Diego. This is a big territory, so be prepared for driving, and some overnights. Thank you for considering the Garratt-Callahan Company. We also have multiple sales openings nationwide. Please visit the career section of our website: www.garrattcallahan.com Requirements: A minimum of 3 years technical sales related to water treatment chemicals is required. Selling to a variety of industrial customers is preferred. CWT is preferred. Knowledge of the Southern California industrial marketplace is preferred. A four-year technical degree is preferred for this position. Military equivalent, such as Navy Nuclear Propulsion, or Army CBRN School, is also great. You will be a successful applicant if you have a technical degree such as Chemistry, Chemical Engineering, Environmental Science, Biology or Mechanical Engineering. NOTE: Garratt-Callahan does not sponsor work visas. No recruiters please. If you have a disability, and need assistance during the application and selection process as a result, please contact the Garratt-Callahan Human Resources department at 650.697.5811. Arrangements can be made to provide an accommodation in order to assist you in applying for an open position using our on-line system, completing any other related paperwork, interviewing, or any other portion of the employment process. This phone line is only for disability assistance. When requesting an accommodation, please provide your name, phone, email address, or any other means of contacting you. Provide a brief description of the nature of the requested accommodation. A member of the Human Resources team will then contact you to discuss your request. A request for an accommodation will not affect your opportunities for employment with Garratt-Callahan. Garratt-Callahan values differing experiences, backgrounds and perspectives among our employees, and see them as a competitive advantage. Garratt-Callahan is committed to the fair and equal treatment of all associates and applicants. Garratt-Callahan is an equal opportunity employer that evaluates qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. • The “Equal Employment Opportunity is the Law” poster is available at: http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf • Garratt-Callahan Company’s reaffirmation of Equal Employment/Affirmative Action Statement http://www.g-c.com/documents/humanresources/EEOLetterJeffGarratt.pdf Key Words: Chemistry, chemicals, scientific, science, salesperson, salesman, saleswoman, outside sales, technical sales, account representative, account executive, territory sales, territory manager, district sales, district manager, field engineer, field service, AE, sales engineer, chemical engineer, chemist, mechanical engineer, biologist, biology, microbiology, nalco, ecolab, barclay, chemtreat, veralto, solenis, Evoqua, Xylem,Hach, chem-aqua, kurita, Veolia, kemira, suez, buckman, Pentair, global water technologies, water treatment, boilers, cooling towers, waste water, pumps, equipment, chillers, polymers, biocides. San Diego.

Job Description Patent Prosecution Associate – AmLaw 100 Firm Locations: Various Full-Time Direct Counsel represents an AmLaw 100 firm seeking a Patent Prosecution Associate with 1–4 years of experience to join its intellectual property practice. The ideal candidate will have experience in patent prosecution, patent bar membership, and a strong technical background in the life sciences, chemistry, or related disciplines. This role involves supporting patent prosecution matters for innovative clients across biotechnology, pharmaceutical, and emerging health technology sectors. Qualifications: • 1–4 years of patent prosecution experience at a law firm, • Registration with the U.S. Patent and Trademark Office (Patent Bar required), • Advanced degree required in one of the following fields: cell or molecular biology, immunology, biochemistry, bioinformatics, bioengineering, organic chemistry, medicinal chemistry, cancer biology, pharmacology, biophysics, or digital health-related disciplines, • Prior patent agent experience preferred, • Strong academic credentials, • Excellent written, verbal, and interpersonal communication skills Compensation & Benefits The expected salary range is $225,000–$310,000, depending on experience and year classification. Discretionary merit-based bonuses may also be awarded. The firm offers a competitive benefits package, including healthcare coverage, retirement benefits, paid parental leave, wellness programs, professional development support, paid CLE and bar expenses, and additional employee benefits. Direct Counsel is conducting a confidential search for qualified candidates.

Job DescriptionAbout TruvianWant to join a fast-paced, innovative company that is transforming the future of blood testing? Truvian is a healthcare technology company operating at the intersection of diagnostics and consumer technology. We have developed an automated benchtop diagnostic platform that delivers laboratory-quality results in minutes across a broad range of health tests.Our proprietary, FDA-cleared technology is designed to make blood testing more accessible, convenient, and affordable by providing comprehensive results from a single small blood sample in minutes throughout a broad range of locations. We are continuing to advance our technology’s capabilities to further redefine point-of-care testing and bring high-quality healthcare closer to where patients need it most.To us, our work at Truvian is more than a job – It’s a mission. We are a culture dedicated to discovery and empowerment. We are trailblazers on the path to put health information where it belongs - in the hands of the individual. We are partners in the belief that talented people, working as a team, can make every day an adventure. Come join us as we realize our vision to make routine health testing convenient, affordable, and actionable for today’s connected consumers!Job SummaryTruvian is seeking a driven Quality Control Technician to support our Quality Control team for approximately 3–6 months. This is a temporary position. This is a hands-on, bench-based position responsible for supporting in-process testing of bulk materials, reagents, consumable kits, and finished products. The Quality Control Technician will perform testing on Truvian’s automated blood-testing platform by following established standard operating procedures. Responsibilities will include routine operation and maintenance of laboratory equipment, assembly of test components, evaluation of test results, and accurate documentation of observations and results. This individual will work closely with Quality Control team members, scientists, engineers, Manufacturing, and other cross-functional partners to support testing, product release, troubleshooting, and laboratory operations. The successful candidate will bring strong attention to detail, sound documentation practices, flexibility, and a team-oriented approach. This position will report to the Manager, Quality Control. Location and Work Arrangements Location: San Diego, CA (Onsite) This role requires regular onsite work. We welcome applications from qualified candidates; however, relocation assistance is not provided for this position. Candidates should be located within commuting distance of the office. Visa Sponsorship Candidates must be authorized to work in the United States on a full-time basis. Truvian does not currently provide visa sponsorship or support employment-based immigration petitions for this role. Work Schedule This position offers multiple shift and schedule opportunities. Available shifts may include First Shift and Swing Shift, with workweek schedules of Monday–Friday, Tuesday–Saturday, or Wednesday–Sunday or an alternative workweek schedule of four 10-hour days, Sunday through Wednesday. Final shift and schedule assignments will be based on position availability and business needs. Here’s Why You Will Love this Job: • You will have a hands-on, participant-facing role supporting clinical studies at Truvian to generate data that substantiate the performance of Truvian's breakthrough blood testing technology., • You'll work with a rock-star team of people who are passionate about the work they do and our ability to disrupt healthcare with our innovative products., • You’ll be part of a team responsible for the company’s growth and product launch., • You’ll thrive in a fast-paced, dynamic environment where you can implement fresh ideas and new processes and make things happen quickly without a bunch of red tape., • You’ll have great perks such as generous benefits (Medical/Dental/Vision/EAP/Paid Life Insurance/LTD/401K), accrued vacation, and on-site wellness perks.What You Will Do, • Perform routine Quality Control testing of bulk materials, reagents, consumable kits, and finished products., • Operate the Truvian automated blood-testing platform according to approved procedures and training., • Follow established test methods, standard operating procedures, specifications, and acceptance criteria., • Evaluate test results and promptly escalate unusual results, discrepancies, or potential quality issues., • Accurately document observations, activities, and test results in accordance with Good Documentation Practices., • Support the timely completion, review, and transmission of Quality Control test data., • Assist with investigations by gathering information, documenting findings, and preparing investigation summaries., • Perform routine operation, cleaning, and maintenance of laboratory equipment., • Verify equipment readiness and calibration status before use., • Assemble test parts, consumables, or other components as required., • Support troubleshooting activities, assay validation, and other special laboratory projects as assigned., • Collaborate cross-functionally to support product release and resolve testing or documentation issues., • Follow current Good Manufacturing Practices and Truvian’s Quality Management System, policies, procedures, and training requirements., • Help maintain a clean, organized, and safe laboratory environment., • Assist with restocking laboratory supplies and maintaining inventory., • Participate in process and operational improvement activities., • Manage multiple responsibilities and adapt to changing priorities., • Perform other duties as assigned.What You Will BringRequired Qualifications, • Bachelor’s degree in Biology, Chemistry, Biochemistry, or a related scientific discipline, or an equivalent combination of education and relevant experience., • Minimum of 3 years of Quality Control, laboratory testing, manufacturing testing, or other directly related experience., • Familiarity with laboratory or quality testing methods., • Experience following standard operating procedures, test methods, work instructions, or established laboratory protocols., • Experience documenting laboratory observations and test results accurately and completely., • Strong organizational and prioritization skills., • Strong attention to detail and the ability to carefully follow written instructions., • Ability to recognize defects, discrepancies, and unusual test results., • Strong verbal and written communication skills., • Ability to work independently while contributing effectively within a team., • Ability to manage multiple assignments and complete tasks by established deadlines., • Flexibility to respond to changing operational demands and priorities., • Ability to identify and distinguish between colors.Preferred Qualifications, • Experience in a medical device, diagnostics, biotechnology, pharmaceutical, or other regulated environment., • Experience working under current Good Manufacturing Practices., • Familiarity with Quality Management Systems and Good Documentation Practices., • Experience operating automated laboratory instruments or diagnostic platforms., • Experience with reagent, consumable, in-process, or finished-product testing., • Exposure to nonconformance investigations, troubleshooting, product release, or assay validation.The benchmark requires a scientific degree with a minimum of 3 years of experience, while also allowing equivalent experience. It emphasizes quality testing methods, Quality Management System knowledge, organization, communication, attention to detail, independence, deadline management, and defect recognition. Supervisory Role No Compensation $22.00 to $26.00 per hour The hourly range for this position represents the anticipated range for qualified candidates. Compensation decisions are based on a variety of factors, including relevant experience, skills, education, training, certifications, internal equity, market data, and business needs. The final compensation offered to a successful candidate will be determined based on these factors and the requirements of the role. Physical Demands and Abilities • Regularly use hands to handle laboratory materials, equipment, components, and testing supplies., • Frequently stand, walk, stoop, kneel, crouch, or move within the laboratory., • Occasionally sit, climb, or balance., • Lift and move up to 5 pounds repeatedly and safely., • Possess the close, distance, color, peripheral, and depth vision necessary to perform detailed laboratory work., • Maintain the ability to adjust focus when inspecting materials, components, and test results.Interested candidates are encouraged to submit a cover letter along with their resume. The cover letter is an opportunity to highlight how your experience in assay and/or panel architecture aligns with our mission, your approach to technical leadership and cross-functional collaboration, and how your expertise has driven innovation in diagnostic product development and complex assay systems. Truvian is an Equal Opportunity Employer and is committed to fostering a diverse, inclusive, and respectful workplace. Employment decisions are made based on qualifications, merit, and business needs. Truvian prohibits discrimination, harassment, and retaliation and does not discriminate on the basis of any characteristic protected by applicable federal, state, or local law, including race, color, religion, creed, sex, pregnancy (including childbirth, breastfeeding, and related medical conditions), gender, gender identity, gender expression, sexual orientation, national origin, ancestry, age, physical or mental disability, medical condition, genetic information, marital status, military or veteran status, reproductive health decision-making, or any other legally protected status. This policy applies to all aspects of employment, including recruitment, hiring, placement, promotion, compensation, benefits, training, transfers, leaves of absence, disciplinary actions, termination, and all other terms and conditions of employment. Truvian is also committed to providing reasonable accommodations to qualified individuals with disabilities and to applicants and employees with sincerely held religious beliefs, practices, or observances, in accordance with applicable law. Powered by JazzHR IyskQvidX6

Job Description Laboratory Technician (Wet Lab Testing)Overview We are seeking a detail-oriented Laboratory Technician to support high-volume testing operations in a fast-paced laboratory environment. In this role, you will perform routine wet lab testing, prepare buffer solutions, operate laboratory equipment, and execute standardized testing procedures while ensuring accuracy, consistency, and compliance with established protocols. This position is ideal for candidates who thrive in structured, process-driven environments and enjoy hands-on laboratory work supporting product quality, validation, and continuous improvement initiatives. Key Responsibilities • Perform wet lab testing, including drift, linearity, and other analytical testing procedures., • Prepare buffer solutions, reagents, and testing materials according to established protocols., • Set up and maintain controlled laboratory testing environments., • Execute detailed testing procedures and accurately document results., • Conduct visual inspection, imaging, and evaluation of test samples and components., • Maintain laboratory equipment, supplies, and work areas to ensure operational readiness., • Support data entry, recordkeeping, and sample traceability activities., • Follow Standard Operating Procedures (SOPs) and laboratory safety requirements at all times., • Collaborate with Quality, R&D, Engineering, and Manufacturing teams to support testing activities., • Contribute to a quality-focused culture through accurate, repeatable, and reliable test execution.Required Qualifications, • Hands-on experience in a laboratory environment performing wet lab testing., • Experience preparing buffer solutions and working in controlled testing environments., • Proficiency using laboratory equipment, glassware, measuring devices, and standard testing tools., • Strong attention to detail and ability to follow written procedures with precision., • Understanding of laboratory safety practices and quality standards., • Ability to perform repetitive testing tasks while maintaining a high level of accuracy., • Strong organizational and documentation skills.Preferred Qualifications, • Experience performing drift, linearity, validation, or qualification testing., • Previous experience in a high-volume or production-style laboratory environment., • Experience with visual inspection, imaging systems, or sample evaluation., • Exposure to regulated environments such as GMP, GLP, ISO, or FDA-regulated settings., • Experience handling structured data entry and maintaining test records., • Proficiency with Microsoft Excel and Microsoft Office applications., • Associate's or Bachelor's degree in Biology, Chemistry, Life Sciences, or a related scientific field preferred.Work Environment, • Schedule: Monday-Friday, 7:00 AM-3:30 PM, • Fast-paced, high-volume laboratory environment with approximately 100 testing procedures., • Collaborative team environment consisting of approximately 29 laboratory professionals., • Frequent interaction with cross-functional teams including Quality, R&D, Manufacturing, and Engineering., • Quality-driven culture focused on accuracy, consistency, and continuous improvement.Why Join the team?, • Opportunity to work in a cutting-edge laboratory supporting critical testing operations., • Collaborative and supportive team environment., • Exposure to cross-functional projects and regulated laboratory processes., • Strong opportunity to develop laboratory, quality, and validation testing experience.Job Type & Location This is a Contract position based out of San Diego, CA. Pay and Benefits The pay range for this position is $25.00 - $25.00/hr. Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave) Job Type & Location This is a Contract position based out of San Diego, CA. Application Deadline This position is anticipated to close on Nov 4, 2026. Workplace Type This is a fully onsite position in San Diego,CA. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records. Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

Job DescriptionCompany Description At Sobi, we believe diversity drives innovation and inclusion creates stronger teams. We are committed to building a workplace where everyone feels valued and empowered to contribute. If this role excites you but you’re unsure if you meet every requirement, we encourage you to apply. Your unique perspective and experiences could be exactly what we need. We look forward to hearing from you! At Sobi, each person brings their unique talents to work as a team and make a difference. We are dedicated to developing and delivering innovative therapies to improve the lives of people who live with a rare disease. Our edge comes from our team of people and our commitment to patients. Our mission and culture at Sobi North America get us excited to come to work every day, but here are a few more reasons to join our team: • Competitive compensation for your work, • Generous time off policy, • Opportunity to broaden your horizons by attending popular conferences, • Emphasis on work/life balance, • Collaborative and team-oriented environment, • Making a positive impact to help ultra-rare disease patients who are in need of life saving treatmentsJob Description Sobi is hiring for 3 Sr MSL, Lymphoma (Lacutamab) openings. Candidates can work remotely anywhere in the continental U.S., with a strong preference that they're located within 30-40 minutes of a major airport. As the Senior Medical Science Liaison (MSL), Lymphoma (Lacutamab), you will serve as a field-based scientific expert on cutaneous T-cell lymphoma (CTCL) and lacutamab, a humanized monoclonal antibody immunotherapy targeting KIR3DL2. You will build trusted scientific relationships, exchange balanced medical information, and generate actionable insights that inform US Medical Affairs strategy and launch readiness. You will support Sobi's rare disease portfolio in the hematology franchise and serve as a trusted scientific resource across the hematology-oncology, dermatology, and dermato-oncology communities. You will collaborate with academic, community, and multidisciplinary care teams, always in accordance with regulatory, legal, and compliance requirements. This is a field execution role within Hematology Medical Affairs. You will contribute insights and a field perspective to the CTCL medical strategy, which is led by Medical Affairs leadership. What You Will Do Scientific Engagement and External Relationships • Serve as a primary field-based scientific point of contact for Sobi Medical Affairs within your assigned geography., • Develop and maintain meaningful, two-way relationships with opinion leaders, healthcare professionals, medical organizations, investigators, and other stakeholders involved in CTCL care., • Exchange accurate, fair, balanced, and scientifically rigorous information on CTCL, lacutamab, relevant clinical data, disease biology, treatment approaches, and the evolving care landscape., • Engage across academic, community, and multidisciplinary settings, including hematology-oncology, dermatology, and dermato-oncology practices., • Respond appropriately to unsolicited scientific inquiries and connect stakeholders with Sobi resources in line with applicable policies and procedures. Medical Insights and Strategy Execution • Identify, document, and share high-quality field insights on unmet needs, clinical practice, patient pathways, evidence gaps, stakeholder perspectives, competitive developments, and the treatment landscape., • Partner with Medical Affairs leadership and cross-functional colleagues to interpret insights and inform adjustments to medical strategy, tactics, educational priorities, and engagement plans., • Execute territory-level medical plans aligned with the US CTCL and lacutamab medical strategy, adapting engagement to local and regional stakeholder needs., • Support key institution and stakeholder engagement planning, helping establish Sobi as a trusted scientific partner in CTCL. Launch Readiness, Education, and Congress Support • Contribute to lacutamab launch preparedness through disease-state education, articulation of unmet need, scientific exchange, stakeholder mapping, and field execution of approved medical tactics., • Provide internal and external scientific training on CTCL disease biology, preclinical science, clinical data, evidence gaps, and relevant outcomes., • Participate in or support advisory boards, medical roundtables, webinars, symposia, and other educational activities at local, regional, and national levels., • Represent Sobi Medical Affairs at scientific and medical congresses, and synthesize and communicate key updates and implications to internal stakeholders., • Collaborate to identify and develop field resources and scientific materials specific to CTCL and lacutamab. Evidence Generation and Clinical Development Support • Provide field-based support to Clinical Development and Clinical Operations, including site identification and recommendations, investigator engagement, communication facilitation, site initiation support, and patient accrual support., • Identify evidence gaps and potential research opportunities, and communicate them to appropriate internal partners., • Contribute scientific and field perspectives to evidence generation activities, real-world evidence initiatives, publications, and medical education programs, as appropriate., • Support investigator-sponsored research and other research collaborations in accordance with company processes and governance. Cross-Functional Collaboration and Territory Leadership • Partner with colleagues in Medical Affairs, Medical Information, Clinical Development, Market Access, Patient Advocacy, Commercial, Legal, Compliance, and other functions, while maintaining the independence and integrity of the Medical Affairs role., • Serve as a scientific resource to internal stakeholders and contribute to cross-functional initiatives consistent with Medical Affairs objectives and company guidelines., • Demonstrate excellence in territory planning, stakeholder prioritization, documentation, follow-through, and management of multiple projects and competing priorities., • Contribute to the broader Field Medical organization's success by sharing best practices, supporting colleagues, and fostering a collaborative, respectful, patient-focused culture. What Success Looks Like Success in this role is marked by: • Scientific credibility and curiosity, • Strategic territory leadership, • Insight generation and synthesis, • Trusted stakeholder partnership, • Cross-functional collaboration, • Clear, balanced communication, • Agility and a solution-oriented approach, • Operational excellence, • A patient-centered mindsetQualifications Required and Preferred Qualifications • Education: Accredited doctorate degree in a life-science, health-science, or basic-science discipline, such as PharmD, PhD, DNP, DSc, MD, or DO., • Candidates with another advanced health degree and extensive relevant industry or clinical experience may be considered., • Experience: At least 5 years of MSL experience in hematology/oncology, heme-onc, or a closely related therapeutic area is required., • Further experience in the following is highly valued:, • Clinical practice, Cutaneous T-cell lymphoma (CTCL), Peripheral T-cell lymphoma (PTCL), lymphoma, dermatology, dermato-oncology., • Rare disease and/or product launch., • Scientific acumen: Strong ability to understand, critically evaluate, and clearly communicate complex scientific and clinical information., • Clinical hematology-oncology background is highly preferred., • Knowledge of CTCL and/or PTCL and the multidisciplinary care environment is an advantage., • Patient focus: Strong commitment to patient needs and advancing scientific understanding within the CTCL community. Location, Travel, and Work Environment • Remote, field-based position supporting an assigned US geography., • Frequent domestic travel by ground and/or air is required (60% or more), depending on territory size, stakeholder needs, congress participation, and business requirements., • Ability to attend local, regional, and national meetings, including occasional evening or weekend programs, as business needs require., • Ability to work effectively from a remote office and manage a geographically dispersed territory. Additional Information Compensation and Total Rewards at Sobi At Sobi, we are dedicated to providing our employees with a comprehensive and industry-competitive total rewards package. Our compensation philosophy is designed to recognize and reward talent, ensuring that your contributions are valued and reflected in your overall rewards. Your total compensation at Sobi goes beyond just your base salary and annual bonus. It also includes a robust suite of benefits, such as: • A competitive 401(k) match to support your financial future., • Tuition and wellness reimbursements to invest in your personal and professional growth., • A comprehensive medical, dental, and vision package to prioritize your health and well-being., • Additional recognition awards to celebrate your achievements. The base salary range for this role is $215,000 - $230,000. Each individual offer will be determined based on several factors, including your experience, qualifications, and location. Additionally, this role is eligible for both short-term and long-term bonuses, as outlined in the plan details. All Sobi employees need to demonstrate behaviors in line with Sobi's core values: Care, Ambition, Urgency, Ownership and Partnership. Are you ready to be on the Sobi team? Come join a culture that empowers every person to be the person that makes a difference for rare disease. Why Join Us? We are a global company with over 1,900 employees in more than 30 countries and are committed to the societies where we operate. With a deeply skilled management team directing our day-to-day wins, and a Board with a stellar track record, we’re ready to take on the world’s diseases, ailments and adversity. Our people believe they have the power to make a positive impact in others’ lives because that’s exactly what we do here. If you’re seeking a career that taps into your talents in a way that makes the world a better, healthier place, we just may have a job for you. We know our employees are our most valuable asset, and our culture conveys that. We offer a competitive benefits package, to support the health and happiness of our staff. Sobi Culture At Sobi, we refuse to accept the status quo. This is because we have witnessed first-hand the challenges facing those affected by rare diseases, and have used this knowledge to shape our business to find new ways of helping them. As a specialized biopharmaceutical company, we are dedicated to rare diseases. And we see this focus as a strength. By effectively turning our research into ground-breaking treatments, we help make medicine more accessible and open up more possibilities for patients and more opportunities for those caring for them. This has been our approach since day one, but we know we can’t change the world of rare diseases on our own. Accomplishing this requires strong partnerships with patients, partners and stakeholders across the entire value chain. Together, we define how our business can create solutions that serve the needs of those affected by rare diseases while facilitating sustainable growth. An Equal Opportunity Employer Sobi is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at Sobi are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity, protected veterans and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status or protected groups by the laws or regulations in the locations where we operate. If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access this website to apply for a vacancy as a result of your disability. You can request reasonable accommodations by sending an email to jennifer.partyka@sobi.com. Know Your Rights

Job DescriptionDescription: Company Overview: Vividion is a next generation biotechnology company based in San Diego that is leveraging its proprietary chemical proteomics platform to conduct proteome-wide footprinting of drug-protein interactions with unprecedented breadth and precision. Our technology allows us to screen, identify and optimize novel drugs that selectively bind virtually any protein, including proteins previously considered “undruggable”. Our pipeline and emerging programs reflect a matured and productive platform capable of delivering first in class drugs utilizing novel mechanisms of action (allosteric inhibitors, protein-protein interaction inhibitors, functional activators, degraders etc.) against undruggable targets in the oncology and immunology space. We prize scientific excellence, creativity, team players and we are committed to continued innovation. We have worked hard to create a collaborative and dynamic work culture where your ideas and discoveries are valued and will have an impact. We are growing and there are opportunities for mentorship and career progression. Vividion has been recognized as a Top Workplace by The San Diego Union-Tribune from 2022 to 2025. Job Summary: The VP, Product Team Leader (PTL) serves as the single point of accountability for the integrated strategy, decision process, and execution of assigned pipeline assets. Chairing the Product Team, this leader guides programs from development candidate and IND-enabling activities through clinical proof of concept. The PTL translates scientific, clinical, and commercial opportunities into a differentiated global product strategy and an execution-ready Integrated Development Plan. Working through empowered functional leaders, the PTL aligns scope, timelines, investment, evidence generation, and key inflection points with corporate and portfolio priorities. The role owns the integrated decision process while respecting the decision authority and technical accountability of Clinical Development, Medical, Regulatory, CMC, Safety, Clinical Operations, Biometrics, Translational Science, Commercial, and other functions. Requirements: Key Responsibilities: Strategy and Value Creation • Define the asset vision, target product profile, and value proposition by integrating patient need, scientific rationale, competitive landscape, regulatory opportunity, access, and commercial potential., • Lead indication prioritization, development scenarios, and investment choices, and establish a clear path to proof of concept with an initial view toward registration, commercialization, and lifecycle management., • Adapt strategy as the scientific, clinical, regulatory, and market landscape evolves while preserving optionality and asset value. Product Team and Decision Leadership • Chair a Product Team of empowered leaders across relevant research, development, medical, operational, commercial, legal, and finance functions., • Build an inclusive, high-accountability team culture that supports rigorous debate, transparent communication, timely execution, and collective ownership of program outcomes., • Clarify decision rights and escalation pathways, and lead integrated decisions with clear owners, criteria, options, tradeoffs, timing, and execution plans., • Lead program risk management, scenario planning, contingencies, and escalation of material changes to the appropriate governance forum. Clinical Development and Evidence Generation • Partner with the Chief Medical Officer, Clinical Development leadership, and the Clinical Development Lead to ensure clinical plans are scientifically rigorous, medically appropriate, feasible, and differentiated., • Guide protocol strategy, cohort and indication sequencing, proof-of-concept criteria, dose and regimen decisions, biomarker strategy, data-readout planning, and interpretation of emerging evidence., • Ensure cross-functional readiness for key milestones, including IND/CTA, first patient dosed, cohort expansion, recommended Phase 2 dose, proof of concept, later-stage development, filing, and launch, as applicable., • Participate in key health authority interactions and maintain alignment among regulatory strategy, clinical evidence, CMC readiness, and commercial objectives. Execution and Resource Stewardship • Partner with Program Management to maintain the integrated plan, critical path, decision calendar, risk register, governance cadence, and readiness packages., • Develop and defend program budgets and resource requirements, evaluate time-cost-risk tradeoffs, and ensure execution within approved scope and investment., • Identify cross-program dependencies and constraints, resolve conflicts with functional and portfolio leaders, and recommend enterprise-level tradeoffs., • Drive operational excellence, quality, inspection readiness, and compliance with applicable global requirements. Education and Experience: • Advanced degree (Ph.D., M.D., Pharm.D., or equivalent) required., • 15+ years of progressive pharmaceutical or biotechnology experience, with substantial leadership of complex development programs., • Demonstrated drug-development leadership, including expertise in tumor biology, translational strategy, and the competitive landscape., • Proven success executing global development strategies from early development through proof of concept and participating in major health authority interactions., • Exceptional executive communication and business acumen, with the ability to navigate ambiguity and present clear recommendations to senior leadership. Pay & Benefits: The anticipated base salary for this position ranges from $275,000 to $320,000 depending on relevant skills, competencies, experience, and education. In addition, this position is eligible for target bonus, long-term-incentives, 401k retirement savings plan with company match, and a comprehensive benefits package which includes medical, dental, vision, life, and disability insurance. EEO & Employment Eligibility: Vividion Therapeutics, Inc. is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other characteristic protected by applicable federal, state, or local laws. Privacy Policy: The protection of your personal information is a commitment we take seriously. For information regarding our Privacy Policy (CA candidates) please visit https://vividion.com/privacy-notice/.

Job Description If you are unable to complete this application due to a disability, contact Ocean Associates at 703-388-9548 to ask for an accommodation or an alternative application process. Ocean Associates Inc. (OAI) is seeking an applicant to provide Marine Biologist support to the Southwest Fisheries Science Center in La Jolla, CA. OAI is a Virginia corporation established in 2003 that provides consulting and technical services to the U.S. government, non-governmental organizations, international organizations, and the private sector. We specialize in scientific program and project management, strategic planning, professional and technical services, and stakeholder engagement, supporting government contracts. Background The Southwest Fisheries Science Center’s Marine Mammal & Turtle Division’s (MMTD) primary mission is to assess marine mammals and turtles relative to management objectives in U.S. waters, or oceans where the U.S. has a vested interest under the Magnuson-Stevens Fishery Conservation and Management Act (MSA; including 16 U.S.C. § 1881a/c/d and 16 U.S.C. § 1882-4), the Endangered Species Act (ESA; including 16 U.S.C. §1533, and 16 U.S.C. § 1536), and the Marine Mammal Protection Act (MMPA; 16 U.S.C. 1361 et seq.). The research feeding into our assessment science includes abundance estimation and monitoring of abundance trends, identification of units to conserve, assessing health and condition of individuals in the context of life histories, and understanding ecosystem state (structure and function). MMTD is seeking Marine Biologist support services for laboratory and field work, including but not limited to responding to strandings, shore and ship-based surveys, operating Uncrewed Aerial Systems (UAS), collecting and processing samples from dead and live animals, conducting molecular laboratory and analytical analysis for population and health studies, and various associated administrative tasks. Tasks • Laboratory analysis in support of ESA/MMPA protected species assessments. Assist in conducting laboratory analysis of hormone levels and genetic assessments, reproductive status, population assessments, age determination, and health in marine mammal and turtle tissues (e.g., blood, blubber, skin, serum, teeth, bones, and whale blow)., • Photographic analysis of ESA/MMPA protected species. Assist in conducting analyses of cetacean and marine turtle photographs for species and individual identification, estimation of life-history parameters, and photogrammetry., • Data entry & report assistance. Assist in organizing digital data files, enter data and records into the provided database(s) and digital repositories, conduct data QA/QC protocols, prepare data summary spreadsheets, and provide assistance with writing reports, technical memorandums, and scientific manuscripts., • Participate in site-specific informational meetings and offsite scientific meetings. Participate in periodic SWFSC and MMTD meetings with the Project Lead(s), NMFS staff, and Center leadership. May participate in offsite scientific meetings to present scientific results, exchange information, and stay informed., • Fieldwork in support of ESA and MMPA scientific research survey efforts. Participate in fieldwork/scientific research surveys on an as-needed basis, including driving government vehicles, shore and ship-based surveys, and participating in travel when necessary to complete tasks., • Shipping samples. Assist in shipping samples to other FMCs, organizations, institutions, and universities as needed. This task may require handling and shipping of hazardous materials (e.g., dry ice, formalin, ethanol), which will require current DOT and IATA hazardous material shipping certifications., • Operations support. ssist in completing a variety of administrative tasks, including, but not limited to, curating inventories of supplies and properties, developing paperwork for placing orders, and receiving and storing supplies. Start Date: As soon as possible Location: Southwest Fisheries Science Center in La Jolla, CA. Travel: Travel is anticipated and authorized for this task order. • Participate in gray whale surveys for up to two weeks at a time at Granite Canyon and/or the Piedras Blancas light station, CA per Period of Performance., • Attend conferences and meetings in order to present scientific findings., • Participate in fieldwork in support of protected species research projects., • Exact dates and locations are TBD., • Locations could be either domestic or international. Salary and Benefits: This is a full-time position with benefits. Salary, commensurate with experience, between $25.00 - $28.50 per hour. Requirements Applicants must have the following minimum requirements: • Bachelor's degree, or higher, from an accredited college or university with a major directly related in a field of study as related to the requirements of specific task order with emphasis in biology, fisheries, or oceanography, plus three (3) years of experience in related field. Master’s or doctorate degree in a related field may be substituted for experience., • Experience conducting marine mammal and/or turtle necropsies, • Experience responding to marine mammal and/or turtle strandings, • Experience collecting biological samples and data in the field, • Certification of hazardous material shipping training, • Experience with image analysis, including images of cetaceans collected from boat and aerial platforms for species and individual identification If you are interested in being considered for this position, please APPLY THROUGH OUR ADP WEB PORTAL, AT THE LINK AT THE TOP RIGHT OF THIS PAGE. Only qualified applicants that meet minimum experience or background requirements stated above need apply. When applying for this position you will be asked to upload your resume at the end of this online application. Applicants should submit a resume that includes the following: • Cover letter that briefly describes how you meet the required and preferred qualifications listed., • Work history for past 10 years or since last full-time education., • Education., • Previous experience or training with similar requirements., • Three professional references., • Include your name in the document file name., • Upload your resume in readable, not scanned, PDF or Word format (PDF is preferred). In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States, complete the required employment eligibility verification document form upon hire, and successfully complete a federal government background check. OAI does not discriminate on the basis of any status or condition protected by applicable federal or state law. OAI is a government contractor and is required by law to invite applicants to self-identify their veteran status. OAI is required to use the information it collects as part of its future affirmative action efforts in hiring. The information is collected anonymously by computer and is not connected to your application. You will see a place to check a box in OAI's online application. Even though the information is anonymous, self-identification is voluntary. You can always check the box that says you decline to self-identify. Note: If you are not selected, your materials may be retained for present or future opportunities. We may use your resume in bidding on a project and if we are awarded the work, we will contact you before seeking further applicants. If you do not wish us to retain or use your resume to seek work for you, please let us know in the "Notes" section on the second page of the online application.

Job Description BioLabs is a global innovation infrastructure company creating the physical and community backbone that powers life science discovery worldwide. Through a growing network of premium shared laboratories and coworking spaces, BioLabs provides turnkey access to state-of-the-art research facilities, entrepreneurial programming, and deep industry and capital connections. These integrated ecosystems enable innovators - from early-stage founders to established R&D teams - to rapidly translate ideas into impact without the constraints of traditional lab ownership. The BioLabs network now spans major innovation hubs across the United States, Europe, and Asia, serving as a catalyst for collaboration and a launchpad for breakthroughs that advance human health and sustainability. Learn more at www.biolabs.io. ROLE OVERVIEW BioLabs is seeking to hire a Lab Operations Associate at BioLabs San Diego at our site in San Diego, CA. Reporting to the Lab Operations Manager, the individual in this hands-on role will assist in and coordinate the routine maintenance of a shared laboratory facility while responding to the laboratory and facility-related requests of our resident companies and other staff members, as needed. This position provides an excellent opportunity to support promising startup companies in their most formative years, while developing your own laboratory operations skills in a cutting-edge biotechnology facility. RESPONSIBILITIES • Assist and support the management of the laboratory and facility spaces; assist with ordering for site; assist with keeping all spaces and infrastructure clean and in good repair; assist with receiving and delivery activities for resident packages., • Support laboratory and facility equipment management – assist with installation, calibrations, preventative maintenance, cleaning, and decontamination of laboratory equipment; ensure proper use, care, and training of equipment by staff and residents; help develop, implement, and maintain standard operating procedures for equipment use and care., • Participate in on- & off-boarding of residents and member companies – discuss safety, space tours, badge access, initial equipment and space training, loaned equipment returns, decommissioning of space and preparation of same for new residents., • In collaboration with the site team, contribute to building resident community culture., • Assist the site EHS officer – execute all site-related safety programs in line with corporate EHS policies; assist with all hazardous waste stream activities per all federal, state, and municipal regulations and BioLabs policies; help maintain all chemical inventories and SDS databases., • Provide excellent customer service with a high level of attention to detail., • Other duties as needed. QUALIFICATIONS • Bachelor’s degree in biology/chemistry, genetics, or other related life sciences discipline., • Minimum of one (1) year experience in an academic and/or commercial laboratory environment and in experience in equipment, decontamination and maintenance, chemical and biological waste management, inventory management and ordering., • Familiarity with cellular, molecular, and microbiology techniques., • Customer service focused, with an excellent work ethic and an optimistic attitude., • Detail oriented with specific attention to quality control and a commitment to excellence., • Outstanding organizational skills and ability to prioritize multiple tasks and/or projects., • Must be able to lift over 50 pounds and be able to stand for multiple hours at a time., • Respond to and be available for occasional site and lab-related issues outside regular business hours as part of the on-call rotation., • Be available to attend occasional off-hour events., • Ability to travel to other BioLabs site locations as needed. BioLabs provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Job Description ABOUT GENALYTE At Genalyte, we’re revolutionizing diagnostic testing to empower a healthier future. Genalyte is a San Diego-based diagnostics company developing the Merlin platform, a novel photonic ring resonator-based system designed to deliver rapid, multiplexed diagnostic results. We believe that timely and accurate health insights shouldn’t be a luxury, but a necessity. We are driven by a vision where advanced diagnostic capabilities are accessible, efficient, and seamlessly integrated into healthcare. Genalyte is more than just a laboratory; we are advocates for health empowerment, dedicated to providing insights that can transform lives and communities. WHY WORK FOR US Joining Genalyte at this pivotal pre-commercial stage means your work will have real, visible impact — on our technology, our culture, and ultimately on how diagnostic testing is delivered to patients. Regardless of your role, you'll be part of a collaborative team working closely with leadership to build something meaningful from the ground up. Genalyte offers competitive compensation including base salary, significant equity participation, and a comprehensive benefits package. This is a rare opportunity to grow alongside a high-impact company at a genuinely exciting moment in its journey. POSITION SUMMARY The Research Associate II works independently under supervision to assist and support the designing, optimization and validation of new immunoassays on the Genalyte Merlin(™) platform. In this role, you’ll be responsible for verification and validation testing of new products and changes to released products. The Research Associate II contributes to verification and validation (V&V) activities for multiple systems comprising assays, reagents, consumables, instruments, and software. The role requires a strong detail-focused skill set to execute tests of products exiting development and to further support and improve products within manufacturing. This position works an alternative workweek schedule of four 10-hour days, Sunday through Wednesday. ESSENTIAL FUNCTIONS & RESPONSIBILITIES These may include but are not limited to: Follows established procedures to assist in design analysis on components and/or assemblies to assist in the development process of quantitative immunoassays for submission to the FDA for 510(k) clearance assessing the product under design control process from concept to product launch Works independently under the guidance of a supervisor or senior team member and follows provided instructions to manage laboratory equipment and coordinate test station setups in support of product development, in accordance with established procedures Analyze data for assay and process improvement and report findings to team and senior leadership Executes experiments and validation protocols, supports problem-solving and trouble-shooting activities with guidance from Team Lead & Manager Meet milestones for product development timelines Work as part of a multi-disciplinary team with other chemists, data scientists, engineers and manufacturing personnel Maintain compliance with all company policies, quality systems, design control and procedures Document results, protocols, SOPs, etc Supports product improvement and manufacturing optimization EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS & ABILITIES A Bachelor’s degree in Biology, chemistry, biochemistry or similar with 2+ years of experience in Assay Development Experience with design control, complex systems and assays Experience in GDP/GMP/GLP Experience with team direction and mentorship Experience with FDA and 510(k) submission process preferred Standard assay laboratory equipment (pipets, microscales, vortexers, centrifuges, etc.) Analytical chemistry equipment (fluorimeters, spectrophotometers, chromatography, etc.) preferred General presentation & spreadsheet analysis software TRAVEL REQUIREMENTS Minimal; occasional travel to clinical sites (<10%). PHYSICAL REQUIREMENTS & WORK ENVIRONMENT The work environment characteristics are representative of both an office and laboratory environment and include handling of viral and bacterial hazards as well as infectious or potentially infectious bodily fluids, tissues and samples. Position requires ability to lift up to 20 lbs. on a regular basis. Walking, standing, and sitting for long periods of time (up to 75% of the day) are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Personal protective equipment is required as posted. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. COMPENSATION The base range for this role is $32 - $36 per hour. Individual pay may vary based on job-related skills, experience, and relevant education or training. In addition to base pay, this role includes meaningful equity participation, eligibility for the target bonus plan, and a comprehensive benefits package). EQUAL EMPLOYMENT OPPORTUNITY Genalyte, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristic. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job Description Title: Research Associate I Location: San Diego, CA Duration: 12 Months Summary: Research Associate I responsible for designing and performing experiments while collaborating and communicating effectively. Primary Responsibilities for the Role: Performs minimally complex experiments with input from supervisor. Understands experimental goal and may provide input to the experimental design. Analyzes data from individual experiment with input from supervisor and documents work in laboratory notebook or report. Able to summarize a group of experiments. Effectively communicates with peers and supervisor. May present data in group meetings. Prepares reagents and panels. Additional Responsibilities: Participates in lab maintenance activities. Maintains training log. Ensures proper transportation, handling, and disposal of hazardous, bio-hazardous and/or infectious substances. Operates and calibrates all general lab equipment. With instruction from supervisor, may write study protocols and reports to support part of the project. Knowledge, Skills and Abilities: Good knowledge of GLP. Working knowledge of laboratory safety and record keeping. Strong mathematics skills. Strong written and verbal communication skills. Microsoft Office Suite: Powerpoint, Excel, Word. Education: B.A./B.S. Molecular Biology, Chemistry, Biochemistry or related field Experience: 0 - 2 years post-baccalaureate laboratory experience in academia or industry M.S. without thesis Equivalency: Depending of the area of assignment, directly related experience or a combination of directly related education and experience and/or competences may be considered in place of the state requirements. Example: if a job Level typically requires an Associates' Degree plus 2 years of experience, an equivalent could be included 4 years of experience or a Bachelor's Degree. Occupational Demands Work is performed in both a lab and an office environment. Frequently sits for 4-6 hours per day. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 50lbs. Some occasional travel within the United States. Able to communicate complex information and ideas so others will understand; ability to listen and understand instruction. Ability to apply abstract principles to solve complex conceptual issues. #RESCIE1

Job Description ARS Pharmaceuticals is a fast-growing, innovative company dedicated to transforming the treatment of severe allergic reactions with neffy®, the first and only FDA-approved needle-free epinephrine product. If you're motivated to make a meaningful impact, this is your opportunity to join a collaborative, entrepreneurial, and inclusive culture. This is a hands-on role that will work an onsite hybrid schedule at our San Diego corporate office in the Carmel Valley area. The Manager / Senior Manager Quality Assurance owns batch disposition and product complaint management for products made at our contract manufacturing organizations (CMOs). You will review executed batch records, drive deviations and investigations to closure, and run the complaint process end to end so that every lot released meets cGMP and regulatory requirements. This is a hands-on role working daily with CMO quality teams, Regulatory, Supply Chain, and Medical Affairs. ESSENTIAL DUTIES & RESPONSIBILITIES: Batch record review and disposition • Review executed batch records, packaging records, and certificates of analysis from CMOs for accuracy, completeness, and cGMP compliance., • Verify that deviations, OOS/OOT results, and change controls tied to each lot are closed or properly assessed before release., • Prepare lot disposition packages and recommend release, rejection, or quarantine; act as QA approver per delegation., • Review master batch records and specifications for new and revised products., • Track batch release timelines and partner with Supply Chain to meet commercial and clinical supply needs. Product complaint management • Own the product complaint process: intake, triage, CMO investigation requests, trending, and closure within defined timelines., • Assess complaints for reportability (e.g., Field Alert Reports, MDRs for combination products) with Regulatory and Pharmacovigilance., • Lead or support root cause investigations and confirm CAPAs are effective., • Prepare complaint trend reports for management review and Annual Product Reviews. CMO Quality Oversight • Serve as day-to-day QA contact for assigned CMOs and testing labs., • Review and approve CMO deviations, investigations, change controls, and CAPAs affecting our products., • Manage quality agreements and quality metrics; join business reviews and person-in-plant visits as needed., • Support CMO audits and regulatory inspections. GMP compliance and quality systems • Maintain compliance with 21 CFR Parts 210/211, 21 CFR Part 4 (combination products), ICH Q7–Q10, and EU GMP as applicable., • Author and revise SOPs for batch disposition and complaint handling., • Contribute to Annual Product Reviews, recall readiness, and inspection readiness., • Lead process improvements, and represent QA on cross-functional project teams. KNOWLEDGE, SKILLS, AND ABILITIES: • Quality judgment: makes sound, documented release and reportability decisions under time pressure., • Partner management: holds CMOs to standards while keeping relationships productive., • Communication: writes clear investigation summaries and explains risk to non-QA colleagues., • Ownership: tracks open items to closure without being chased., • Primarily office-based work with occasional travel to CMO sites, including time in GMP manufacturing areas with gowning. Occasional after-hours support for urgent complaints or release needs. EDUCATION AND EXPERIENCE: Required • Preferred Bachelor's degree in chemistry, biology, pharmacy, engineering, or related science. An acceptable combination of education and relevant experience will also be considered, • Minimum of 6+ years of QA experience, • Hands-on batch record review and lot disposition for commercial pharmaceutical or combination products., • Direct experience managing product complaints, deviations, and CAPAs., • Working knowledge of cGMP (21 CFR 210/211), ICH guidelines, and FDA expectations., • Experience overseeing CMOs or external testing labs in a virtual or outsourced model., • Strong technical writing and attention to detail. Preferred • Drug-device combination product experience (21 CFR Part 4, 820 / QMSR)., • Sterile, nasal, or inhalation dosage form experience., • Electronic QMS experience (e.g., Veeva Vault QualityDocs/QMS, MasterControl)., • ASQ certification (CQA, CQE, or CPGP). At ARS, we are proud to offer a highly competitive compensation & benefits package. The full-time salary range for this posted position is $145,000 to $185,000 and may be eligible for a discretionary annual performance bonus. Actual pay rates are determined by considering multiple factors including qualifications, relevance of experience, education & credentials, subject matter expertise, and other job-related factors permitted by law. This position is also eligible for Equity, 401k matching, and our excellent benefits package including 100% employer paid Medical, Dental & Vision for employees. View the full package here: ARS Careers Page ARS Pharmaceuticals believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. ARS Pharmaceuticals is also committed to providing reasonable accommodation to qualified individuals so that an individual can perform their job-related duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at careers@ars-pharma.com The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications.

Job Description Patent Agent (Molecular Biology) Locations: Boston, MA; Palo Alto, CA; Philadelphia, PA; San Diego, CA; Washington, DC Direct Counsel is seeking a Patent Agent to join a leading global law firm’s Patent Development and Strategy Group. The ideal candidate will have 3–5 years of experience preparing and prosecuting patent applications, a degree in molecular biology or a related scientific discipline, and registration with the USPTO. Responsibilities: Draft and prosecute patent applications and responses to USPTO office actions. Collaborate with attorneys on patent preparation and prosecution matters. Prepare instructions to foreign patent agents in response to office actions. Conduct patentability studies and prepare related assessments. Provide technical support for opinions, due diligence projects, and litigation. Maintain a thorough understanding of relevant products and technical developments. Requirements: 3–5 years of experience preparing and prosecuting patent applications. Bachelor's degree in molecular biology or a related scientific discipline; a master's degree is preferred. Registration with the USPTO. Excellent written and verbal communication, research, analytical, and organizational skills. Strong attention to detail and the ability to manage competing priorities in a fast-paced environment. Preferred Qualifications: Experience in patent litigation, opinions, licensing, patent due diligence, and/or patent prosecution. Compensation: $120,000–$225,000 annually, depending on geographic market, experience, qualifications, and other relevant factors.

Job Description Requirements: • B.S. Degree in Computational Biology, Computer Science, or field as outlined in the essential duties., • Familiarity with the development of bioinformatics pipelines within Next Generation Sequencing and PCR applications., • Familiarity with production software development lifecycle., • Familiarity with best practices for software development (such as Git, agile, code reviews, CI/CD)., • Ability to effectively communicate software system designs., • Excellent communication skills (both written and oral) with the ability to communicate complicated ideas and information effectively at all levels., • Demonstrated ability to perform the essential duties of the position with or without accommodation. Preferred Qualifications:, • Experience with programming languages, ideally Python., • Familiar with automated software testing, preferably in the context of medical devices software such as bioinformatics analysis pipelines., • Familiarity with container orchestration concepts and systems, e.g. Docker, Kubernetes, etc., • Familiar working with cloud platforms (AWS, GCP, Azure)., • Familiarity within an FDA-Regulated, Medical Device, Pharmaceutical, Biotech, or other regulated industry, developing CFR 21 Part 11 and IEC 62304 compliant software., • Familiarity with medical device requirements such as Quality System Regulation (21 CFR part 820) ISO 14971 Medical Device Risk Management, ISO 13485, etc. Work experience is strongly preferred., • Familiarity with bioinformatics analysis pipeline frameworks., • Familiarity with software related Cybersecurity risk management such as FDA Cybersecurity guidance, IEC27000 series, IEC 15408, etc. as well as software audits is a plus., • Familiar with managing requirements in a validated RM tool such as JAMA, DOORS, etc.

Job Description About Tr1X Tr1X is a clinical-stage biotechnology company developing engineered Tr1 cell therapies to restore immune balance in autoimmune and inflammatory diseases. Leveraging the unique biology of Tr1 cells, the company is advancing a pipeline of off-the-shelf allogeneic and in vivo CAR-Tr1 therapies designed to deliver targeted immunoregulation and address diseases driven by immune dysfunction, including transplant-related complications. Founded by pioneers in the discovery of Tr1 cells, Tr1X, Inc. is focused on developing durable, potentially curative therapies for conditions with high unmet need. For more information, visit www.tr1x.bio. Position Summary The Director, Clinical Operations provides strategic leadership and operational oversight for the implementation and execution of clinical trials from study start-up through close-out. The Director is accountable for leading cross-functional clinical study teams; directing contract research organizations (CROs), study vendors, and investigative sites; and ensuring all clinical trial activities are executed in alignment with corporate objectives, timelines, budgets, regulatory requirements, GCP guidelines, and internal SOPs. This role serves as a key operational leader within the organization and is responsible for mentoring, developing, and supervising clinical operations personnel. Key Responsibilities • Provide strategic leadership as the Clinical Study Lead for cross-functional teams to ensure study start-up, enrollment, maintenance, and close-out activities are executed on schedule, within budget, and in accordance with quality expectations., • Direct and oversee all aspects of clinical study management to ensure operational excellence, inspection readiness, and delivery of high-quality clinical data., • Lead the clinical operational development, review, and finalization of clinical trial protocol synopses, protocols, protocol amendments, and other key study-related documents., • Lead the CRO and vendor selection strategy for outsourced activities, including RFP development, bid management, proposal evaluation, budget negotiations, and executive-level vendor selection decisions., • Direct negotiation, execution, and oversight of contracts and scopes of work with CROs, study vendors, consultants, and investigative sites., • Oversee the development and maintenance of critical study documents, including informed consent templates, management plans, study trackers, and operational plans, ensuring appropriate delegation and accountability., • Chair and lead internal and external clinical study meetings, governance reviews, and cross-functional operational discussions, ensuring alignment of objectives, decisions, and action items., • Partner strategically with Regulatory Affairs to ensure timely preparation and submission of site essential regulatory documentation to the FDA and other regulatory authorities., • Develop and oversee clinical monitoring strategies and monitoring plans to ensure compliance, quality oversight, and operational consistency across studies and vendors., • Provide strategic oversight for case report form (CRF) design, edit check development, and data collection methodologies in partnership with Data Management and Clinical Development., • Lead site initiation planning and execution activities, including oversight of training materials, presentations, and investigator engagement strategies., • Provide leadership and governance oversight of CROs, field monitors, and clinical vendors to ensure contractual obligations, quality metrics, and operational deliverables are achieved., • Establish oversight processes for monitoring visit reports, protocol deviations, CAPAs, and action item resolution to ensure quality and compliance standards are maintained., • Direct and oversee study-wide operational activities including vendor management, biospecimen handling, investigational product logistics, investigator payments, data quality oversight, and centralized records management., • Lead the review and analysis of clinical data reports to identify operational, safety, and efficacy trends and communicate findings to cross-functional leadership and governance committees., • Ensure Trial Master File (TMF) oversight and inspection readiness throughout the duration of all assigned studies., • Lead and facilitate internal clinical program meetings, investigator meetings, safety review committees, and other cross-functional governance forums., • Partner with departmental leadership to define and execute clinical development operational strategies, resource planning, and process optimization initiatives., • Proactively identify operational risks and implement mitigation strategies to ensure study continuity, compliance, and successful execution., • Travel to clinical sites, investigator meetings, and vendor locations as required, up to 15%., • Foster a culture of accountability, collaboration, operational excellence, and continuous improvement within a fast-paced, dynamic clinical development environment., • Perform additional strategic and operational responsibilities as required to support evolving business and clinical development objectives. Required Qualifications & Experience • Bachelor's degree in a scientific or healthcare-related discipline with a minimum of 10 years of progressive clinical operations experience, including at least 5 years of direct sponsor clinical study management and leadership experience., • Demonstrated leadership experience managing complex global or multi-center clinical trials across multiple phases of development., • Experience in cell and/or gene therapy clinical trials preferred, particularly within Multiple Sclerosis, Inflammatory Bowel Disease, or other autoimmune indications., • Extensive working knowledge of ICH/GCP guidelines, FDA regulations, and global clinical trial regulatory requirements., • Proven ability to lead cross-functional teams, influence stakeholders, and drive strategic clinical operations initiatives in a fast-paced environment., • Strong operational leadership skills with demonstrated expertise in study start-up, trial execution, vendor oversight, risk management, and inspection readiness., • Experience supporting pre-NDA programs and Phase 1 first-in-human clinical trials, including operational strategy, study oversight, monitoring, and close-out activities., • Advanced experience with clinical trial systems including eTMF, CTMS, EDC, safety databases, and other clinical technologies., • Exceptional strategic thinking, problem-solving, organizational, communication, and executive presentation skills., • Ability to independently manage competing priorities while leading within a matrixed cross-functional organizational structure., • Demonstrated success mentoring and developing high-performing clinical operations teams., • High level of professionalism, integrity, accountability, and business acumen. Other Requirements • Legally authorized to work for any employer in the U.S., • Travel is required up to 15%., • The position is based on-site in San Diego, CA. The job responsibilities and requirements provided above are intended to describe the general nature of the work performed by individuals assigned to this job classification. It is not intended to be an exhaustive list of all duties and requirements. Tr1X retains the right to add, change, or delete duties, education, experience or any other requirements of the position at any time. Working at Tr1X At Tr1X, our team is united by a singular shared mission: to transform patients' lives through breakthrough science. We are a group of skilled experts driven by urgency, innovation and a collaborative spirit. Our culture thrives on excellence, positivity, persistence and the agility to tackle new challenges head-on. With an unwavering commitment to patients, science and one another, we foster an environment where team members feel engaged, supported and empowered to make a meaningful impact. We envision a world where autoimmune diseases are not just being treated but are cured. Base Pay Range Anticipated: $210,000 - $230,000 Tr1X considers a variety of factors to determine salary such as education, years of experience, time in the position level, training, knowledge, skills, geographic location, and the market value of the position. Compensation and Benefits Tr1X provides a fair and competitive total rewards program that includes base salary; discretionary annual target bonus; incentive stock options; 401(k) retirement plan with company contribution; health and welfare insurance plans for employees (and their families) that include medical, dental, vision, long-term and short-term disability, and life insurance; paid time off (PTO); and paid holidays. Tr1X embraces a diverse, open, and inclusive environment and believes a strong culture connection is key to success. Tr1X is committed to fairness in recruitment, hiring, transfer, promotion or any other employment practice without regard to race, color, citizenship, national origin, ancestry, religion, sex, pregnancy, marital status, sexual orientation, gender, gender identity and expression, age, physical and medical disability, medical condition, genetic information, political affiliation, protected veteran status, or any other characteristic protected by law. If you are an individual needing assistance to complete an employment application or would like to request an accommodation, please contact the Human Resources department at careers@tr1x.bio. Notice to Employment Agencies The Tr1X talent acquisition program is managed through internal resources, and unsolicited referrals and resumes are not accepted from employment agencies, unless advance written authorization is granted from the human resources department. Tr1X shall not be liable for any fees arising from any unsolicited or unauthorized candidate information received relative to position vacancies.

Job Description Analytical Development Scientist (Temporary) Pay Rate: Up to $37.37/hour Duration: 12-month contract Hours: Full-Time Location: San Diego, CA (Onsite) Summary We are seeking a hands-on Analytical Development Scientist to support the development of analytical methods for biologics, including adeno-associated virus (AAV)-based gene therapies and monoclonal antibodies (mAbs). In this role, you will develop, optimize, troubleshoot, and transfer analytical potency assays, with a primary focus on cell-based functional potency methods. You will also support ligand-binding, molecular, and biochemical assays to ensure analytical methods are robust, reproducible, and appropriate for the stage of product development. The ideal candidate has strong laboratory skills, experience with cell-based assay development, and the ability to collaborate with cross-functional teams and external partners. What You'll Do • Develop, optimize, and troubleshoot cell-based functional potency assays, particularly for AAV-based gene therapies, • Design and execute assays to evaluate transgene expression, biological activity, viral transduction, infectivity, and mechanism-of-action-related endpoints, • Investigate assay variability and optimize experimental parameters to improve robustness, accuracy, and reproducibility, • Analyze and interpret experimental data, assess assay performance, and apply appropriate statistical evaluations, • Maintain accurate laboratory records and ensure data integrity throughout experimental activities, • Support analytical method and knowledge transfers to internal quality control (QC) laboratories and external contract development and manufacturing organizations (CDMOs), • Prepare and review analytical procedures, standard operating procedures (SOPs), qualification and validation protocols, technical reports, and method transfer documentation, • Support analytical method comparability assessments, troubleshoot technical issues, and contribute to analytical control strategy development, • Collaborate with cross-functional teams to establish reliable, reproducible, and phase-appropriate analytical methods What You Bring • PhD in Molecular Biology, Cell Biology, Virology, Biochemistry, or a related field; or a Master's degree with at least 3 years of relevant industry experience; or a Bachelor's degree with at least 5 years of relevant industry experience, • Strong technical expertise in mammalian cell culture, cryopreservation, cell banking, and aseptic techniques, • Hands-on experience developing, optimizing, and troubleshooting cell-based potency assays, • Experience with one or more of the following analytical techniques:, • Cell-based potency assays, including transduction, infectivity, or functional protein expression assays, • Molecular assays, including qPCR, ddPCR, or RT-qPCR, • Flow cytometry and cell-based imaging, • Protein characterization techniques, including Western blotting, capillary electrophoresis, and ELISA, • Meso Scale Discovery (MSD) assays, • Strong analytical, problem-solving, and data interpretation skills, • Excellent written and verbal communication skills, • Strong organizational skills and the ability to collaborate effectively with cross-functional teams, • Ability to work onsite in San Diego, CA Bonus Points If You Have • Experience developing AAV gene therapy potency assays, particularly mechanism-of-action-based functional assays, • Understanding of AAV biology, viral transduction mechanisms, and transgene expression, • Experience developing potency assays for monoclonal antibodies or other biologics, • Familiarity with LC-MS/MS or chromatographic separation techniques, • Knowledge of analytical method qualification, validation, and lifecycle management in accordance with ICH Q2(R2), • Experience transferring analytical methods to QC laboratories or external CDMOs TCWGlobal is an equal opportunity employer. We do not discriminate based on age, ethnicity, gender, nationality, religious belief, or sexual orientation. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Job Description At BioAgilytix, we are passionate about premier science and the impact it has on our world. Our team of highly experienced scientists and professionals deliver tailored services for supporting new medicine breakthroughs with best-in-class bioanalytical services. We are tirelessly committed to our customers by being solution-oriented and deadline-driven. . . and we are growing. Our culture is fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You’ll gain experience with a variety of challenges all while you enable life-changing, life-saving therapeutics to the patients who need them. In this role, you will support LC-MS/MS method validation studies and the analysis of biological samples. Our clients trust us to deliver excellence in data and bioanalysis, and this role is a key part of our project lifecycle. Working alongside a team of expert scientists, you will gain hands-on experience with sample preparation and LC-MS/MS instrumentation across projects involving small molecules, proteins, peptides, and/or biomarkers. Each project brings opportunities to build your technical skills and deepen your understanding of bioanalytical testing. Essential Responsibilities • Compile/process data (make power export), • Prepare summary tables, • Peer review raw data, • Order reagents, • Participate in assay development and validation, • Run assays independently; (biomarker, cell-based, immunogenicity, immuno-, enzymatic, or LC/MS/MS), • Adhere to provided method/directive, • Prepare buffers, • Use LIMS system, • Participate in sample analysis, • Pipetting, • Adhere to safety requirements, • Keep accurate inventory of supplies for assays, • Responsible for accurate record keeping with regard to sponsor's samples, data, and reports (documentation according to GxP guidelines)Additional Responsibilities, • Other duties as neededMinimum Preferred Qualifications: Education/Experience, • Bachelor's degree in chemistry, biochemistry, biotechnology, biology, immunology, or related field with not less than two (2) years' experience in a scientific laboratory environment; or, • Master's degree in chemistry, biochemistry, biotechnology, biology, immunology, or related field with not less than one (1) year experience in a scientific laboratory environmentMinimum Preferred Qualifications: Skills, • Ability to carry out routine tasks accurately, following strict methodology to carry out analysis, preparing samples and maintaining and operating standard laboratory equipment., • Experience with sample preparation and running established LC-MS/MS assays for bioanalytical sample analysis., • Must work effectively within team to meet objectives under time constraints, • Ability to take direction well and multi-task, • Detail oriented and highly organized, • Experience working in a GxP environment preferred, • Excellent oral and written communication skills, • Proficient in the use of MS Excel and WordSupervisory Responsibility, • This position has no supervisory responsibilitiesSupervision Received, • Frequent supervision and instructions, • Infrequently exercises discretionary authorityWorking Environment, • Primarily laboratory environment, • Exposure to biological fluids with potential exposure to infectious organisms, • Rare exposure to skin and lung irritants, toxic materials, and hazardous waste, • Personal protective equipment required, such as protective eyewear, garments, and gloves, • Routinely uses standard office equipment such as computers, phones, photocopiers, and filing cabinetsPhysical Demands, • Ability to work in an upright and/or stationary position for up to eight (8) hours per day, • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment, • Frequent mobility needed, • Frequent crouching, stooping, with frequent bending and twisting of upper body and neck, • Light to moderate lifting and carrying (or otherwise moves) objects, including laboratory equipment, laboratory supplies, and laptop computer, with a maximum lift of 20 pounds, • Ability to access and use a variety of computer software, • Ability to communicate information and ideas so others will understand, with the ability to listen to and understand information and ideas presented through spoken words and sentences, • Frequently interacts with others to obtain or relate information to diverse groups, • Requires multiple periods of intense concentration, • Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence, • Ability to perform under stress and multi-task, • Regular and consistent attendancePosition Type and Expected Hours of Work, • This is a full-time position, • Some flexibility in hours is allowed, but the employee must be available during the “core” work hours as published in the BioAgilytix Employee Handbook, • Occasional weekend, holiday, and evening work required The hourly pay range listed above reflects BioAgilytix's hiring range for this position. BENEFITS AND OTHER PERKS Medical Insurance (HDHP with HSA; PPO), Dental Insurance, Vision Insurance, Flexible Spending Account (medical; dependent care), Short Term Disability | Long Term Disability Life Insurance, Paid Time Off (4 weeks per year), Parental Leave, Paid Holidays (9 scheduled; 5 floating), 401k with Employer Match, Employee Referral Program COMMITMENT TO EQUAL OPPORTUNITY BioAgilytix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, ancestry, national origin, gender, sexual orientation, marital status, religion, age, disability, gender identity, results of genetic testing, service in the military, or any other group protected by federal, state, or local law. To learn more about how we collect, use, and protect your information, please review our Privacy Policy and Terms of Use. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job Description The Opportunity Virchow Medical is seeking molecular-biology-trained laboratory technicians in the San Diego area for flexible, part-time work processing clinical specimens. This opportunity may be particularly attractive to experienced technicians with clinical lab experience, research associates, or laboratory professionals interested in supplemental work with an emerging precision-oncology company. Assignments will be scheduled according to specimen volume and operational needs. Work must be performed onsite in the San Diego area and may occasionally involve short-notice availability. Responsibilities • Receive, accession, label, and track human clinical specimens., • Perform nucleic acid purification using the Thermo Fisher Scientific KingFisherTM Apex Purification System., • Quantify extracted DNA using a QubitTM fluorometer., • Prepare reagents, buffers, consumables, tubes, and sample plates., • Perform aliquoting, centrifugation, pipetting, sample transfers, and other molecular laboratory preparation steps., • Store DNA, RNA, and other specimen materials under defined conditions., • Maintain accurate chain-of-custody, sample-tracking, and laboratory records., • Follow written standard operating procedures, quality-control requirements, and contamination-prevention practices., • Clean and maintain work areas and laboratory equipment., • Identify and document specimen discrepancies, equipment issues, and deviations from established procedures., • Protect patient confidentiality and comply with applicable biosafety, HIPAA, and laboratory requirements. This position is focused on specimen preparation and nucleic acid processing. It does not include independent diagnostic interpretation or reporting of patient test results. Preferred Qualifications • Bachelor’s degree, associate degree, or formal training in molecular biology, biotechnology, clinical laboratory science, biochemistry, or a related field., • Hands-on experience with DNA or RNA extraction and purification., • Micropipetting skills and experience handling low-volume biological samples., • Experience using the KingFisher Apex or another automated magnetic-bead nucleic acid purification platform., • Experience with Qubit DNA quantification or comparable fluorometric methods., • Familiarity with clinical specimens, sample accessioning, chain of custody, and laboratory information or sample-tracking systems., • Understanding of contamination control and unidirectional molecular-laboratory workflows., • Ability to follow detailed procedures consistently and maintain complete, contemporaneous records., • CLS designation, • California laboratory licensure or certification appropriate to the assigned activities, if required. Ideal Candidate You are meticulous, dependable, comfortable working independently, and understand that the integrity of every downstream molecular result begins with careful specimen handling. You enjoy hands-on laboratory work, can accommodate variable sample volumes, and would welcome flexible assignments supporting better access to precision-oncology testing. Virchow Medical, Inc. is an equal-opportunity employer. Employment decisions are based on qualifications, merit, and business needs without regard to legally protected characteristics. \nCompany Description Virchow Medical, Inc. makes specimen-recovery technologies that unlock molecular information left behind during needle biopsy procedures. Our Crow’s Nest® Biopsy Catchment® System is currently in clinical use at seven U.S. medical centers. Virchow Companion SpecimensTM generated by the system are stored in the Virchow VaultTM, enabling oncologists to order sequencing without relying solely on the adequacy of conventional tissue blocks. Virchow Medical, Inc. makes specimen-recovery technologies that unlock molecular information left behind during needle biopsy procedures. Our Crow’s Nest® Biopsy Catchment® System is currently in clinical use at seven U.S. medical centers. Virchow Companion SpecimensTM generated by the system are stored in the Virchow VaultTM, enabling oncologists to order sequencing without relying solely on the adequacy of conventional tissue blocks.

Job DescriptionAssociate — Corporate (Healthcare & Life Sciences Licensing) Practice: Healthcare & Life Sciences Licensing Experience: Minimum 3 years Type: Full-Time Direct Counsel represents an AmLaw 100 firm seeking a highly qualified Corporate Associate with life sciences licensing experience to join its Healthcare & Life Sciences Licensing Practice in the New York office. This role offers the opportunity to work on cutting-edge licensing matters in the biopharmaceutical and healthcare industries. Key Responsibilities: Advise clients on licensing, collaboration, and strategic transactions in the healthcare and life sciences sectors. Draft and negotiate complex licensing and commercial agreements, including research, development, and commercialization deals. Collaborate with partners and cross-disciplinary teams on transactions involving healthcare providers, pharmaceutical companies, and biotech innovators. Provide strategic guidance on intellectual property, regulatory, and commercial issues affecting licensing arrangements. Qualifications: Minimum of 3 years of life sciences licensing experience. Degree in Biology, Chemistry, or related field, or prior biopharmaceutical industry experience, strongly preferred. Excellent drafting, negotiation, and communication skills. Strong academic credentials and the ability to manage complex transactions in a fast-paced environment.

Job Description Overview Ansible Government Solutions, LLC (Ansible) is currently recruiting Medical Technologists to support the VA Medical Center located at 3350 La Jolla Village Dr, San Diego, CA 92161. Services will be delivered to both the Anatomic Pathology and Clinical Pathology divisions of the facility. Exceptional compensation packages with full benefits are available. Ansible Government Solutions, LLC (Ansible) is a Service-Disabled Veteran-Owned Small Business (SDVOSB) providing Federal customers with solutions in many arenas. Our customers face wide-ranging challenges in the fields of national security, health care, and information technology. To address these challenges, we employ intelligent and committed staff who take care of our customers’ success as if it is their own. Responsibilities • Rotate on a regular basis through the areas in which they have been trained and are competent, • Perform a broad range of laboratory procedures in Blood Bank., • Perform advanced and complex laboratory procedures, recognizing deviation from expected results, analyzing and correcting problems using scientific principles, • Recognize and communicate pre-defined critical results affecting patient care, • Maintain the optimal functioning of laboratory equipment and keep appropriate records for documentation; operate, calibrate, identify malfunctions, repair and perform preventive maintenance of laboratory analyzers, • Perform and document quality control, quality assurance and corrective actions related to test performance using sound statistical principles and theories of performance improvement, • Enter and verify laboratory results in the computer system; recognize deviations from expected results, analyze and correct problems using scientific principles, • Perform other duties as assigned relating to the responsibilities of a Medical Technologist Qualifications • Accredited Bachelors degree in medical laboratory science, medical technology, clinical laboratory science, or a related science (i.e. biology, chemistry, etc.) AND completion of an accredited medical technology clinical practice program (i.e. NAACLS, CAAHEP, ABHES) OR • Accredited Bachelors degree including 16 semester hours in biological science (one course in microbiology), 16 semester hours in chemistry (one course in organic or biochemistry), and one course in mathematics AND two (2) years of post-certification clinical laboratory experience within the last ten (10) years as a certified Medical Laboratory Technician (ASCP-BOC), • A minimum of one (1) year of Medical Technologist experience within the last three (3) years, • Demonstrated knowledge of laboratory medicine techniques and practices, • Demonstrated education and clinical training in the practice of laboratory medicine, • No sponsorship available Pay Range: $29.26 - $51.41 hourly All candidates must be able to: • Sit, stand, walk, lift, squat, bend, twist, and reach above shoulders during the work shift, • Lift up to 50 lbs from floor to waist, • Lift up to 20 lbs, • Carry up to 40 lbs a reasonable distance, • Push/pull with 30 lbs of force All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Powered by JazzHR DgRdMIsBZh

Job DescriptionDocument Management Associate (Temp-to-Hire)Company: BioPhase Location: San Diego, CA (Fully Onsite) Pay Rate: $26.50–$30.00/hr (target ~$28/hr) Employment Type: Temp-to-Hire About the Role BioPhase is seeking a Document Management Associate to support quality and compliance activities within a GMP-regulated environment. This is a fully onsite, temp-to-hire opportunity based in San Diego, ideal for someone with hands-on experience managing controlled documents and supporting audits. Key Responsibilities • Manage and maintain controlled documents and records in accordance with GMP and quality standards, • Support document storage, revision control, access permissions, and archival processes, • Assist with issuing batch records and controlling label stock, • Support internal and external audits by providing requested documentation, • Collaborate with cross-functional teams across Quality, Manufacturing, and Operations, • Assist with SOP drafting, revisions, and training support as needed, • Ensure document integrity, compliance, and confidentiality at all timesQualifications, • Bachelor’s degree in Biology or a related field (or equivalent experience), • 1–2+ years of experience in a GMP Quality or Manufacturing environment, • Familiarity with GMPs and regulated documentation practices, • Experience drafting, revising, or managing controlled documents preferred, • Strong attention to detail and organizational skills, • Comfortable working both independently and in a team-based environmentWork Environment, • Fully onsite in San Diego, • Office-based role with extended computer use, • May require lifting up to 20 lbs occasionally

Job Description Job Title: Research Operations Associate Location: San Diego, CA Type: Contract Compensation: $25-$29.25/hr Work Model: Onsite – onsite Hours: 40.0 Overview The Research Operations Associate plays a critical role in supporting a global Early Research Sciences organization by providing scientific operations, logistics, and administrative support to research teams and external collaborators. This position serves as a key liaison between internal stakeholders and Contract Research Organizations (CROs), ensuring seamless execution of research operations, budget management, data tracking, and sample logistics. Responsibilities • Research Operations & Collaboration Management, • Support scientific teams by coordinating operational activities related to external research collaborations and CRO partnerships, • Facilitate communication and execution between internal stakeholders and external service providers., • Assist in managing research-related agreements, project deliverables, and operational workflows., • Work effectively across a matrixed organization to ensure alignment and timely execution of projects., • Budget & Financial Management, • Track project budgets, expenditures, and financial commitments., • Create and manage purchase orders (POs) and related procurement activities., • Monitor spending trends and support budget forecasting activities., • Generate reports and metrics to help ensure projects remain within approved budgets, • Sample & Logistics Coordination, • Coordinate domestic and international shipment of research materials, compounds, and samples., • Manage import/export activities and ensure compliance with shipping and customs requirements., • Maintain accurate shipping documentation and monitor shipment timelines., • Partner with internal and external stakeholders to ensure successful delivery of research materials., • Data Management & Reporting, • Collect, track, and analyze operational data and performance metrics., • Monitor key performance indicators (KPIs) related to collaborator performance, shipping cycle times, research productivity, and budget utilization., • Support trend analysis and generate operational insights to drive efficiency improvements., • Develop reports, dashboards, and presentations for leadership and project teams., • Administrative & Operational Support, • Maintain accurate records and documentation., • Support ongoing process improvement initiatives., • Prepare presentations, reports, and operational summaries., • Assist with special projects and operational priorities as assigned Requirements, • Bachelor’s degree in Chemistry, Biochemistry, Biology, Organic Chemistry, or a related scientific discipline., • Strong understanding of scientific terminology, chemical compounds, and/or biological materials., • Excellent organizational skills with exceptional attention to detail., • Strong written and verbal communication skills., • Proficiency in Microsoft Office Suite, including Excel, PowerPoint, and Teams., • Ability to manage multiple priorities and work effectively in a collaborative environment., • Demonstrated analytical and problem-solving skills. Preferred Qualifications, • Experience in pharmaceutical, biotechnology, research, or CRO environments., • Experience supporting scientific operations, research administration, logistics, or project coordination., • Knowledge of import/export requirements and international shipping regulations for scientific materials., • Data analysis and reporting experience., • Familiarity with tools such as Spotfire, business intelligence platforms System One, and its subsidiaries including Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #LI- Ref: #558-Scientific

Job Description QC Analyst – Microbiology (Contract) – BioPhase Location: San Diego, CA Assignment: 4-month contract Pay: $33–35/hr Schedule: Monday–Friday, 8:00 am – 5:30 pm About the Role Our client’s Quality Control team is seeking a Microbiology QC Analyst to support critical testing activities in a GMP environment. This role is ideal for someone with strong technical skills in microbiology who thrives in a fast-paced, regulated lab setting. What You’ll Do • Perform microbiology QC testing on in-process, release, and stability samples, • Conduct environmental monitoring and aseptic technique assessments, • Maintain accurate records to ensure compliance with GMP requirements, • Assist with investigations, deviations, and lab support activities, • Collaborate with QA and cross-functional teams to maintain quality standardsWhat We’re Looking For, • Bachelor’s degree in Microbiology, Biology, or related field, • 2+ years of industry QC laboratory experience in microbiology (GMP environment strongly preferred), • Hands-on experience with microbial techniques (bioburden, endotoxin, sterility, environmental monitoring, etc.), • Knowledge of aseptic techniques and cleanroom practices, • Familiarity with deviations, CAPA, and GMP documentation practices, • Strong attention to detail, organization, and ability to work independently

Job Description Are you looking for an opportunity to make a difference? At Mesa Labs we’re passionate about protecting the vulnerable by enabling scientific breakthroughs, ensuring product integrity, increasing patient and worker safety, and improving quality of life around the world. At Mesa Labs we offer competitive wages, including bonus opportunity, and a comprehensive benefits package. Base Compensation Range: $ $33.8942 to $42.4279 USD This position is eligible for an annual 10% bonus opportunity in addition to the base salary Outstanding Benefits and Perks: We are proud to offer a variety of benefits that meet the diverse needs of our employees: • Eligible for benefits the first day of the month after you start, • Tiered Medical, Dental and Vision Insurance options, • Health savings (HSA), healthcare & dependent care flexible spending (FSA) accounts, • Company paid short term and long-term disability (unless covered by a state disability plan), • Company paid life insurance and AD&D, • 3 weeks of accrued vacation time; accruals begin on Day 1, • Paid sick leave of 48 hours per calendar year, • Eligible employees may receive four (4) weeks paid Care Giver leave after 1 year of service or in accordance with state leave laws, • 401(k) plan that provides a 4% Safe Harbor company match on a 4% employee contribution that begins on Day 1, • Employee Wellness and Financial Assistance Resources through Cigna and NY Life, • Nine (9) paid company holidays per year, • Overtime opportunities Agena: Agena Bioscience® empowers research laboratories worldwide to deliver scalable targeted genomic data. Our open, advanced platform, the Mass ARRAY® System, provides researchers with insights through a highly multiplexed solution in the areas of mutation profiling, liquid biopsy, pharmacogenetics, and more. Job Summary: The Research Associate II, Molecular Biology performs a range of molecular biology laboratory procedures in support of technology development, product research, and process improvement initiatives. This role executes established experimental protocols, contributes to assay development and optimization, and supports data collection and analysis under general supervision. The incumbent applies working knowledge of molecular biology principles, follows defined research plans, and collaborates effectively with scientists and cross-functional partners. Duties / Responsibilities Experimental Execution and Support • Performs molecular biology experiments using established protocols, including cloning, PCR, sequencing, and recombinant protein expression and purification., • Assists in the development, optimization, and validation of molecular biology protocols and assays for DNA/RNA manipulation and expression systems., • Conducts routine transcription profiling, hybridization assays, or array-based analyses as assigned., • Executes experiments with attention to detail and reproducibility, escalating issues and deviations as needed., • Data Collection and Documentation, • Collects, compiles, and summarizes experimental data for review by senior scientists., • Maintains accurate and complete laboratory notebooks and electronic records in accordance with company standards., • Assists in preparing technical summaries, data tables, and figures for internal reports and presentations., • Participates in team data reviews and contributes observations and insights. Collaboration and Project Support • Works closely with R&D scientists and project team members to support research and development activities., • Follows project plans and timelines, contributing to assigned tasks and milestones., • Supports troubleshooting efforts by executing directed experiments and documenting outcomes., • Shares technical knowledge and best practices within the laboratory team. Laboratory Operations and Compliance • Maintains laboratory equipment, instruments, and work areas in accordance with safety, quality, and GLP requirements., • Adheres to established protocols, SOPs, and biosafety guidelines., • Ensures proper handling, storage, and disposal of biological materials and reagents., • Participate in continuous improvement initiatives related to laboratory efficiency, organization, and safety. Continuous Learning • Builds technical expertise in molecular biology techniques and laboratory practices., • Stays informed of relevant methodologies and tools through training and on-the-job learning., • Seeks feedback to improve experimental execution and scientific understanding. Experience / Education Bachelor’s degree in Molecular Biology, Biochemistry, Biotechnology, or a related field. 0-2 years of relevant laboratory experience. Knowledge & Skillsets Required • Working knowledge of molecular cloning, PCR, DNA/RNA extraction, sequencing, and recombinant protein expression., • Familiarity with assay execution, protocol adherence, and basic troubleshooting techniques., • Ability to accurately document experimental procedures and results., • Strong attention to detail and organizational skills., • Effective written and verbal communication skills., • Ability to work independently on assigned tasks while collaborating within a team environment., • Commitment to quality, safety, and compliance in laboratory operations. Mesa Labs is an Equal Employment Opportunity Employer. Mesa Labs prohibits unlawful discrimination and harassment against applicants or employees based on age, race, sex, color, religion, creed, national origin or ancestry, disability, military status, sexual orientation, or any other status protected by applicable state or local law. Please note that Mesa Labs conducts criminal background checks upon offer acceptance.

Job DescriptionDescription: Research Associate I (Vivarium)– Job Description ABOUT CERTIS ONCOLOGY SOLUTIONS: Certis Oncology is an AI-enabled translational decision intelligence company dedicated to improving how cancer therapies are discovered, developed, and delivered to patients. We transform data into decisions that accelerate the development of cancer therapies and advance the promise of precision medicine for every patient. Our Oncology Intelligence® platform brings together artificial intelligence, diverse oncology datasets, and experimental validation in patient-derived in vitro and in vivo models to generate actionable insights that help researchers make more confident decisions. By integrating predictive modeling, intelligent data exploration, and biological validation, we help reduce development risk and accelerate the delivery of innovative cancer therapies. The same technologies can be applied to predict therapeutic response for individuals undergoing treatment, helping advance the future of precision oncology. Based in San Diego, we are a multidisciplinary team of scientists, data experts, and innovators united by a common purpose: improving outcomes for cancer patients. Together, we are working toward a future where every therapeutic decision is informed by the full context of available evidence. The Research Associate I (RA1) in the vivarium is responsible for supporting preclinical in vivo studies through hands-on animal work, dosing, surgical procedures, and data collection. The RA1 ensures the accurate execution of study protocols while maintaining high standards of animal welfare, data integrity, and compliance with institutional and regulatory guidelines. Key Responsibilities Study Management • Perform tumor measurements, body weight assessments, and clinical observations according to study protocols., • Record and maintain accurate, timely, and legible data in accordance non-GLP requirements., • Communicate study progress, animal health, and any protocol deviations to the Study Director or senior staff. Dosing Procedures • Perform compound administration via multiple routes including:, • Oral gavage (PO), • Intraperitoneal (IP), • Subcutaneous (SC), • Intratumoral (IT), • Ensure proper dosing techniques, animal handling, and documentation are followed in accordance with SOPs. Study Requirements and Endpoints • Conduct blood collection (via approved routes)., • Perform minor tissue harvesting and animal takedowns at study endpoints., • Follow humane endpoints and ensure compliance with IACUC and institutional animal care policies. Surgical Procedures Must be proficient in and able to independently perform: • Subcutaneous (SC) tumor implants, • Subcutaneous inoculations, • Mammary Fat Pad (MFP) implants, • Mammary Fat Pad (MFP) inoculations In Vivo Support • Prepare mice for surgery, including anesthesia setup and surgical site preparation., • Provide post-operative care and monitoring., • Perform tattooing and ear tagging for animal identification., • Conduct sick mouse care, including documentation and communication with veterinary staff. Qualifications Education & Experience: • Bachelor’s degree in Biology, Animal Science, or a related field, or equivalent relevant laboratory experience., • 0–2 years of experience in a vivarium or in vivo research setting preferred., • AALAS certification (ALAT or higher) desirable but not required. Skills & Competencies: • Strong understanding of rodent handling and restraint techniques., • Demonstrated proficiency with multiple dosing routes and surgical methods., • Excellent attention to detail and ability to follow SOPs and study protocols., • Strong organizational and communication skills., • Commitment to maintaining animal welfare and ethical research standards. Work Environment • Position involves routine handling of laboratory animals (mice)., • Work may require extended periods of standing, bending, and use of personal protective equipment (PPE)., • May require weekend or holiday work depending on study schedules. Reporting Structure This position reports directly to the In Vivo Manager, with functional guidance from senior research associates or team leads. Requirements:

Job Description Requirements: • B.S. Degree in Computational Biology, Computer Science, or field as outlined in the essential duties., • Familiarity with the development of bioinformatics pipelines within Next Generation Sequencing and PCR applications., • Familiarity with production software development lifecycle., • Familiarity with best practices for software development (such as Git, agile, code reviews, CI/CD)., • Ability to effectively communicate software system designs., • Excellent communication skills (both written and oral) with the ability to communicate complicated ideas and information effectively at all levels., • Demonstrated ability to perform the essential duties of the position with or without accommodation. Preferred Qualifications:, • Experience with programming languages, ideally Python., • Familiar with automated software testing, preferably in the context of medical devices software such as bioinformatics analysis pipelines., • Familiarity with container orchestration concepts and systems, e.g. Docker, Kubernetes, etc., • Familiar working with cloud platforms (AWS, GCP, Azure)., • Familiarity within an FDA-Regulated, Medical Device, Pharmaceutical, Biotech, or other regulated industry, developing CFR 21 Part 11 and IEC 62304 compliant software., • Familiarity with medical device requirements such as Quality System Regulation (21 CFR part 820) ISO 14971 Medical Device Risk Management, ISO 13485, etc. Work experience is strongly preferred., • Familiarity with bioinformatics analysis pipeline frameworks., • Familiarity with software related Cybersecurity risk management such as FDA Cybersecurity guidance, IEC27000 series, IEC 15408, etc. as well as software audits is a plus., • Familiar with managing requirements in a validated RM tool such as JAMA, DOORS, etc.

Job DescriptionJob Title: Technical Development Scientist III / Technical Development Principal Scientist Location: San Diego, CA — Onsite Pay Rate: $55.17–$68.97/hour Job Description • Develop, optimize, and adapt analytical methods for cell therapy product characterization and release using Design of Experiments (DoE)., • Design and execute exploratory studies to define Critical Quality Attributes (CQAs) and improve analytical methods., • Lead analytical method development, transfer, qualification, validation, and lifecycle management activities supporting process development, product release, characterization, and stability., • Perform analytical method risk/gap assessments, remediation, and robustness improvements., • Establish analytical control strategies, trending approaches, control charts, and capability assessments., • Analyze experimental data, interpret study outcomes, and develop recommendations for analytical and process development activities., • Support technology transfer of analytical methods to QC laboratories and ensure methods are fit-for-purpose., • Author SOPs, assay development and qualification reports, and regulatory documentation supporting CMC and regulatory filings., • Apply analytical development expertise to cell therapy products, including stem cell and T-cell platforms.Education, • Master's degree in Immunology, Molecular Biology, Biochemistry, or related scientific discipline with 6–9+ years of analytical development, QC, technology transfer, or method lifecycle management experience., • OR Ph.D. in Immunology, Molecular Biology, Biochemistry, or related scientific discipline with 2+ years of industry experience.Required Skills, • Flow cytometry and immunology analytical method development., • Analytical method transfer to QC laboratories., • Cell therapy analytical development and product characterization., • Analytical method optimization, remediation, qualification, and validation., • CMC technology transfer and analytical control strategies., • Design of Experiments (DoE), experimental design, and analytical data analysis., • Control charts and process/analytical capability assessments., • ICH guidelines, cGMP, USP, and regulatory requirements applicable to analytical development and method qualification/validation., • Analytical method lifecycle management and assay trending.Preferred Skills, • 2+ years of cell therapy industry experience., • Analytical control systems for stem cell and T-cell products., • ddPCR, qPCR, cell imaging, reporter-based potency assays, cell engineering, Next-Generation Sequencing (NGS), or metabolic analysis., • Experience supporting cell therapy CMC and regulatory filings. If you are interested in hearing more about the position, please respond to this posting with your resume attached. Please forward this posting to any friends or colleagues as we do offer a Referral Bonus for any candidate hired. By applying for this job, you agree to receive calls, AI-generated calls, text messages, or emails from and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy at Privacy Policy

Job DescriptionPosition Details: Research Associate - USCAJP00017663 Primary Work Location: 9860 Mesa Rim Road, San Diego, CA 92121 Work Arrangement: Hybrid – 50% in office and 50% onsite at clinical study sites, as applicable. Candidates should live within a reasonable commute distance of the ATRI office. Equipment Provided: USC will provide a laptop and work cell phone. Job Title: Clinical Research Associate – Clinical Monitor Number of Openings: 3 Pay Rate: $44.00/hour Duration: 6-7+ months Work Hours: 8 hours per day; schedules may vary depending on travel and project requirements. Dress Code: Business casual, especially when visiting clinical study sites. Parking: Free parking at the ATRI office. Interview Process: Two-step interview process. Job Description: The USC Keck School of Medicine – Alzheimer's Therapeutic Research Institute (ATRI), located in San Diego, California, is an academic research institute comprised of scientific collaborators dedicated to advancing the development of new treatments for Alzheimer's Disease through innovative clinical trials. The Clinical Research Associate – Clinical Monitor will oversee clinical trial activities at assigned study sites, ensuring studies are conducted, documented, and reported in compliance with study protocols, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and applicable regulatory requirements. Key Responsibilities: • Conduct onsite and remote monitoring visits, including co-monitoring activities at assigned clinical study sites., • Review Investigator Site Files, study data, Informed Consent Forms, and other essential clinical trial documentation., • Perform Investigational Product (IP) reconciliation and other required monitoring activities., • Ensure clinical study sites comply with GCP, regulatory requirements, study protocols, and ATRI policies., • Identify, document, and follow up on protocol deviations and compliance concerns., • Review clinical study data, issue and resolve queries, and verify inclusion and exclusion criteria for study participants., • Conduct monitoring reviews of electronic Case Report Forms (eCRFs) to ensure data accuracy, participant safety, and protocol compliance., • Serve as the primary point of contact for assigned clinical study sites., • Maintain a thorough understanding of study protocols, procedures, and manuals., • Collaborate with the Lead Clinical Monitor/Lead CRA to escalate site compliance issues., • Participate in monitoring activities to support study milestones and timelines., • Utilize internal systems and study-specific software and tools., • Assist with training new clinical monitors on study-specific procedures and onsite monitoring processes., • Participate in sponsor, internal, and regulatory audits as needed., • Support electronic Trial Master File (eTMF) documentation and filing activities., • Experience in Alzheimer's Disease research is preferred. Candidate Qualifications: Must-Haves: • Minimum 2–3 years of Clinical Research Associate (CRA) experience., • Experience reviewing medical records and clinical trial documentation., • Strong attention to detail and accuracy., • Understanding of clinical trial monitoring and regulatory compliance., • Ability to conduct onsite and remote monitoring visits. Nice-to-Haves: • Experience conducting study closeout visits., • Investigational Product (IP) management and reconciliation experience., • Strong critical-thinking and problem-solving skills., • Proactive approach to identifying and resolving site issues., • Alzheimer's Disease (AD) clinical research experience. Education and Experience: • Education: Bachelor's degree in Healthcare, Health Administration, Biology, Psychology, or a related field. An equivalent combination of education and experience may be considered., • Experience: At least 2 years of relevant experience. Travel Requirements and Reimbursement: This role will require travel to various locations throughout the United States. Important: At this time, the specific travel locations have not yet been determined. Travel destinations will depend on project needs, and additional details will be shared as they become available. Out-of-Town Travel: When travel is required, the following expenses may be reimbursed: • Airfare, • Uber or other approved ground transportation, • Hotel accommodations, • Meals during business travel All reimbursements are subject to applicable limits and require receipts or proof of payment. Local Travel: • Mileage: When using a personal vehicle for project-related travel, mileage reimbursement is available for eligible travel exceeding 50 miles., • Parking: Required parking fees associated with project visits will be reimbursed., • Mileage Calculation: Reimbursable mileage is calculated from the ATRI office to the assigned project site., • Commuting Exclusion: Mileage reimbursement does not apply to regular commuting between the employee's home and assigned work location. All reimbursements are subject to applicable limits and documentation requirements. Regards, Adarsh Singh Sr. Technical Recruiter Cell: (973) 507-7564 Email: Adarsh.Singh@artech.com LinkedIn: linkedin.com/in/adarsh-singh-71ba1b1b9 360 Mt. Kemble Avenue, Suite 2000, Morristown, NJ 07960 Website: www.artech.com

Job Description Overview Ansible Government Solutions, LLC (Ansible) is currently recruiting Medical Technologists to support the VA Medical Center located at 3350 La Jolla Village Dr, San Diego, CA 92161. Services will be delivered to both the Anatomic Pathology and Clinical Pathology divisions of the facility. Exceptional compensation packages with full benefits are available. Ansible Government Solutions, LLC (Ansible) is a Service-Disabled Veteran-Owned Small Business (SDVOSB) providing Federal customers with solutions in many arenas. Our customers face wide-ranging challenges in the fields of national security, health care, and information technology. To address these challenges, we employ intelligent and committed staff who take care of our customers’ success as if it is their own. Responsibilities • Rotate on a regular basis through the areas in which they have been trained and are competent, • Perform a broad range of laboratory procedures in Chemistry, Hematology, Coagulation, Urinalysis, Microbiology, and Transfusion Medicine, • Perform advanced and complex laboratory procedures, recognizing deviation from expected results, analyzing and correcting problems using scientific principles, • Recognize and communicate pre-defined critical results affecting patient care, • Maintain the optimal functioning of laboratory equipment and keep appropriate records for documentation; operate, calibrate, identify malfunctions, repair and perform preventive maintenance of laboratory analyzers, • Perform and document quality control, quality assurance and corrective actions related to test performance using sound statistical principles and theories of performance improvement, • Enter and verify laboratory results in the computer system; recognize deviations from expected results, analyze and correct problems using scientific principles, • Perform other duties as assigned relating to the responsibilities of a Medical Technologist Qualifications • Accredited Bachelors degree in medical laboratory science, medical technology, clinical laboratory science, or a related science (i.e. biology, chemistry, etc.) AND completion of an accredited medical technology clinical practice program (i.e. NAACLS, CAAHEP, ABHES) OR • Accredited Bachelors degree including 16 semester hours in biological science (one course in microbiology), 16 semester hours in chemistry (one course in organic or biochemistry), and one course in mathematics AND two (2) years of post-certification clinical laboratory experience within the last ten (10) years as a certified Medical Laboratory Technician (ASCP-BOC), • A minimum of one (1) year of Medical Technologist experience within the last three (3) years, • Demonstrated knowledge of laboratory medicine techniques and practices, • Demonstrated education and clinical training in the practice of laboratory medicine, • No sponsorship available Pay Range: $29.26 - $51.41 hourly All candidates must be able to: • Sit, stand, walk, lift, squat, bend, twist, and reach above shoulders during the work shift, • Lift up to 50 lbs from floor to waist, • Lift up to 20 lbs, • Carry up to 40 lbs a reasonable distance, • Push/pull with 30 lbs of force All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Powered by JazzHR 9oKusGlLSA

Job Description Validation Engineer- Contract DO WORK THAT MATTERS Client Rapid Diagnostics (formerly Alere) is part of Client's Diagnostics family of businesses, bringing together exceptional teams of experts and industry-leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions. At Client, diverse ideas, perspectives, and expertise allow us to create life-changing solutions that help people live healthier lives. In 150 countries and with businesses spanning nutrition, diagnostics, medical devices, and branded generic pharmaceuticals, Client offers you enormous opportunities to explore your interests and help you achieve your career and personal goals. Client is looking for an outstanding Validation Engineer-Contractor who will effectively lead quality related validation activities to support the Quality Management System. The end goal is to deliver consistent and high-quality validation and supporting documentation for design and development organization. This role requires strong technical, communication, interpersonal and organizational skills, and a solid understanding of the application of FDA, ISO 13485, ISO 14971 standards and company strategies. This opportunity is available with Infectious Disease Developed Markets (IDDM) Business unit within Client, at our location in Towne Centre San Diego, CA. This job description will be reviewed periodically and is subject to change by management. Technical Writing Write procedures, investigations, protocols, deviations, CAPA's, reports, change controls, etc. to support ARDx Towne Centre site departments. Perform and document investigations related to validation activities and performs risk assessments of equipment, processes and systems to determine the scope of validation efforts. Generates validation documentation as required (URS, FRS, DRS, FAT, DQ, engineering studies, IOQ, PQ, PV) for cleaning, shipping, sterilization, facilities, utilities, systems, equipment qualification/requalification, computer system validation, spreadsheets, test method validation and process validation. Writes and/or revises IQ, OQ, PQ related documents, including any or all of the following: SOP's, validation master plans, guidelines and execution plans, automation test plans and technical documents. Responsible for writing Standard Operating Procedures related to Validations and responsible for training Quality Assurance and R&D personal in the validation processes. Service Delivery Performs on site or support work, including but not limited to: Validation protocol executions for FAT/SAT/IQ/OQ/PQ/PV. Equipment Qualification test execution. Investigations and deviations. Provides gap analysis, risk management, risk assessment, risk analysis and validation strategy. Data integrity assessments and review of client data Executes protocols and resolves deviations/discrepancies, analyzes data and writes reports. Performing and supervising thermal mapping of temperature-controlled units, Laboratories, warehouses, etc. Ensures that validations are documented using Good Documentation Practices and are in compliance to FDA, ISO 13485, and Client Policies and Procedures. Evaluate impact on legacy qualifications/validations and determines the scope of re-validation. Support the continuous improvement to the Quality Management System, with a specialty focus on validation processes. Responsible for maintaining a Site Master Validation Plan and ensuring that critical Performance Qualification and/or Process Validations are performed per established schedule. Identify and propose remediation for existing and potential validation issues; provide technical expertise and provide solutions to maintain compliance. Assist with internal and external audits. Manages validation metrics. Manages change control for validation deliverables in the electronic documentation management system. Participate in multiple, concurrent projects. Develops timelines and tracks project status on assigned projects. Keeps stakeholders informed on the status of important projects. Performs other duties as assigned by Management. BASIC QUALIFICATIONS | EDUCATION: Bachelors' degree (B.S.) in a Science related field (Engineering, Biology, Chemistry or equivalent) 5 years of related work experience in a medical device industry with strong technical competency in performing equipment qualification (IQ/OQ/PQ), facility/lab qualification, process validations and excel spreadsheet validations. Proficient understanding of Design Control, Good Documentation Practices (GDP), and current Good Manufacturing Practices (cGMP) Significant experience with application of the FDA regulations and recognized standards (e.g., FDA 21 CFR 820.30, FDA 21 CFR 820.70, FDA 21 CFR Part 11, ISO 13485, ISO 14971, cybersecurity) PREFERRED QUALIFICATIONS: Experience in validation of In Vitro Diagnostic Lab equipment (e.g., Real- Time PCR System, Freezers, Refrigerators, Environmental Chambers, Incubators) and Thermal Mapping, Computerized System Validation. Experience supporting ISO 13485 inspections and FDA inspections. Experience in a multi-site development environment. Experience in compliance management within a rapid-growth, dynamic organization. Statistical or Lean Six Sigma background Working experience with GAMP5 and FDA's Computer Software Assurance initiatives Working experience with Agile, Maximo and ViewLinc. COMPETENCIES: Good working knowledge of Excel and Microsoft Word software Working knowledge of quality techniques such as root cause analysis, 5 why's, and Ishikawa diagrams. Excellent problem solving and decision-making skills. Self-starting, detail oriented, and ability to focus on task at hand Initiative to work towards goals with minimal supervision Ability to work independently with multiple departments to resolve Validation issues Must be able to work effectively in a fast paced, cross-functional team-oriented environment Well-developed English written and verbal communication skills An equal opportunity employer, Client welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities.

Job Description About Tr1X Tr1X is a clinical-stage biotechnology company developing engineered Tr1 cell therapies to restore immune balance in autoimmune and inflammatory diseases. Leveraging the unique biology of Tr1 cells, the company is advancing a pipeline of off-the-shelf allogeneic and in vivo CAR-Tr1 therapies designed to deliver targeted immunoregulation and address diseases driven by immune dysfunction, including transplant-related complications. Founded by pioneers in the discovery of Tr1 cells, Tr1X, Inc. is focused on developing durable, potentially curative therapies for conditions with high unmet need. For more information, visit www.tr1x.bio. Position Summary The Senior Director, Quality (SD) reports to the Chief Technical Officer and is responsible for all aspects of the quality organization including support and oversight for all internal and external GxP operations inclusive of clinical quality assurance (CQA). As the leader of the quality function, the SD establishes and maintains a culture of quality across the organization and is responsible for overseeing development, implementation, and continuous improvement of all quality systems to ensure that all products, processes, and operations comply with applicable regulatory requirements. The SD is ultimately responsible and accountable for critical decisions that directly impact product integrity, patient safety, regulatory compliance, and business continuing. The SD works with both internal and external stakeholders to manage timelines, meet internal deliverables and develop a best-in-class quality organization. This position develops, leads, and coaches the teams responsible for quality systems, quality control, document control, quality assurance, clinical quality, and compliance. The SD responsibilities include implementation and continuous improvement of policies, procedures and standards necessary to ensure compliance with applicable GxPs. Additional responsibilities include team building, career development, assisting with financial reviews, establishment of annual budgets and identification and rollout of yearly goals and objectives and longer-term strategic plans for the department. Key Responsibilities • Provide oversight of quality risks and report risks to senior stakeholders., • Manage a global audit program to ensure vendor/supplier performance and compliance, including development and presentation of meaningful metrics and summaries., • Oversee maintenance of quality management system that collects, stores, establishes control and provides governance for the use of GxP data., • Ensure compliance with all regulatory requirements and industry standards, including FDA, EMA, and ICH guidelines., • Provide strategic direction and guidance to the quality team, ensuring alignment with company objectives and goals., • Drive continuous improvement initiatives to enhance the efficiency and effectiveness of quality processes and systems., • Represent the company in interactions and maintain strong relationships with regulatory agencies, external partners, industry groups, and internal stakeholders., • Partner with clinical operations, CROs, and other key clinical staff to ensure clinical trials are conducted per GCP guidelines., • Monitor and assess quality metrics and KPIs to identify trends and areas for improvement., • Collaborate with cross-functional teams to ensure quality considerations are integrated into all aspects of product development, manufacturing, distribution, and clinical study design/execution., • Conduct regular audits and inspections to assess compliance and identify potential risks and areas for improvement., • Foster a culture of quality and compliance throughout the organization through training, communication, and recognition programs., • Stay current with industry trends and developments and make recommendations for incorporating new technologies and approaches to enhance quality operations., • Lead and mentor a team of quality professionals, providing guidance, feedback, and development opportunities., • Perform other responsibilities as may be required by business needs. Required Qualifications & Experience • B.S. degree in a scientific discipline, including pharmaceutical, biologics, or a related field., • Minimum 12 years of related experience in the pharmaceutical or biotech Industry at FDA regulated manufacturing sites within quality operations., • Minimum 5 years of leadership/management experience within quality with at least 3 years of direct supervisory experience of technical/quality professionals., • Background in biologics or cellular therapy manufacturing., • Experience in hosting regulatory agency inspections and successfully presenting product and quality compliance programs to regulatory agency reviewers., • Advanced knowledge of FDA/ICH regulations, GxP quality systems and operational excellence required for the manufacture of cellular therapeutic products., • General working knowledge of GCP/CQA., • Demonstrated ability to perform long-term project planning with meaningful timelines and budget forecasting., • Ability to prioritize multiple tasks, work under timeline pressures, and drive tasks to completion., • Effective verbal and written communication and solid time management and organizational skills., • Proficiency with Microsoft Office suite software (Word, Excel, PowerPoint, etc.). Other Requirements • Legally authorized to work for any employer in the U.S., • Position is on-site in San Diego, CA The job responsibilities and requirements provided above are intended to describe the general nature of the work performed by individuals assigned to this job classification. It is not intended to be an exhaustive list of all duties and requirements. Tr1X retains the right to add, change, or delete duties, education, experience or any other requirements of the position at any time. Working at Tr1X At Tr1X, our team is united by a singular shared mission: to transform patients' lives through breakthrough science. We are a group of skilled experts driven by urgency, innovation and a collaborative spirit. Our culture thrives on excellence, positivity, persistence and the agility to tackle new challenges head-on. With an unwavering commitment to patients, science and one another, we foster an environment where team members feel engaged, supported and empowered to make a meaningful impact. We envision a world where autoimmune diseases are not just being treated but are cured. Base Pay Range Anticipated: $240,000 – $270,000 Tr1X considers a variety of factors to determine salary such as education, years of experience, time in the position level, training, knowledge, skills, geographic location, and the market value of the position. Compensation and Benefits Tr1X provides a fair and competitive total rewards program that includes base salary; discretionary annual target bonus; incentive stock options; 401(k) retirement plan with company contribution; health and welfare insurance plans for employees (and their families) that include medical, dental, vision, long-term and short-term disability, and life insurance; paid time off (PTO); and paid holidays. Tr1X embraces a diverse, open, and inclusive environment and believes a strong culture connection is key to success. Tr1X is committed to fairness in recruitment, hiring, transfer, promotion or any other employment practice without regard to race, color, citizenship, national origin, ancestry, religion, sex, pregnancy, marital status, sexual orientation, gender, gender identity and expression, age, physical and medical disability, medical condition, genetic information, political affiliation, protected veteran status, or any other characteristic protected by law. If you are an individual needing assistance to complete an employment application or would like to request an accommodation, please contact the Human Resources department at careers@tr1x.bio. Notice to Employment Agencies The Tr1X talent acquisition program is managed through internal resources, and unsolicited referrals and resumes are not accepted from employment agencies, unless advance written authorization is granted from the human resources department. Tr1X shall not be liable for any fees arising from any unsolicited or unauthorized candidate information received relative to position vacancies.

Job Description Job Title: Scientist II – Scientific Applications Location: San Diego CA 92130 Schedule: Onsite - Full time - 8am-5pm Pay Rate: $62.50/hour Required Qualifications • Bachelor’s degree in Immunology, Cell Biology, Biological Sciences, Biotechnology, or a related life science field., • 0–2 years of relevant laboratory experience., • Hands-on laboratory experience through academic research, internships, industry positions, or equivalent experience., • Basic understanding of immunology and experimental design principles., • Strong attention to detail and laboratory execution skills., • Ability to work effectively in a team environment., • Strong scientific communication skills and ability to communicate experimental results clearly., • Ability to manage multiple projects and deadlines., • Curiosity and willingness to learn new technologies and techniques. Job Overview We are seeking a Scientist II to support scientific research, product evaluations, and application development within a scientific applications team. This role contributes to generating scientific data and developing technical materials that support product commercialization. Working under the guidance of senior scientists, the successful candidate will assist with flow cytometry studies, scientific collaborations, experimental workflows, and data analysis. This is an excellent opportunity for someone with foundational laboratory experience and a strong interest in immunology and flow cytometry to develop their technical expertise. Key Responsibilities • Perform and support flow cytometry experiments following established protocols., • Develop expertise in immunology research, flow cytometry, and panel design best practices., • Prepare biological samples, cell cultures, reagents, controls, and instrument setups in accordance with laboratory procedures., • Collect, organize, and analyze flow cytometry and related experimental data., • Assist with optimizing staining panels, sample preparation methods, and assay workflows under the guidance of senior team members., • Maintain accurate laboratory records, study documentation, and experimental reports., • Contribute to scientific presentations, technical reports, application notes, posters, and customer-facing materials., • Conduct literature searches and summarize scientific findings relevant to ongoing projects., • Collaborate with cross-functional teams to support research, product development, and commercialization activities., • Support internal and external studies demonstrating product performance and application utility., • Follow company policies, training requirements, and laboratory safety procedures., • Participate in Environmental, Health, and Safety programs and promote a safe laboratory environment. Preferred Qualifications • Exposure to flow cytometry, immunology, cell culture, molecular biology, or related laboratory techniques., • Experience with data analysis software such as FlowJo or similar platforms., • Experience using flow cytometers., • Proficiency in Microsoft Office applications, including Excel, PowerPoint, and Word. Additional Information This position offers the opportunity to develop hands-on expertise in flow cytometry workflows, experimental design, data analysis, and scientific communication while contributing to collaborative scientific projects.

Job DescriptionCompany Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. 2025, Eurofins generated total revenues of EUR € 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Eurofins BPT- Advantar is looking for a Scientist to join our Routine Testing team located in San Diego, CA. This position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). Responsibilities include completing work under cGMP and/or GLP guidelines for studies, documentation, etc. Assisting in conducting, monitoring and reporting studies to ensure data accuracy and report quality. Providing somewhat complex analytical work on projects and studies using a range of analytical techniques and instruments. Working with increasing independence on studies and assignments. The ideal candidate would possess: • Experience in Biochemistry analytical techniques, both chromatographic and electrophoretic in a GMP environment., • Demonstrated technical experience running HPLC/UPLC, LC/MS, CE, icIEF, Karl Fisher, UV/Vis, and/or SoloVPE instruments, • Experience with LIMS system desirable., • Experience assisting with peer reviewing data, • Comfortability working with multiple software systems and Excel, • A highly motivated staff member that is willing to work on a team, and willing to work with others to teach and learn new skills., • Good organizational skills; ability to follow directions and good communication skills are requiredQualifications, • Bachelor’s degree in relevant field such as chemistry, biochemistry, biology, chemical engineering, sciences, or other directly related field or degree with comparable coursework in the above areas and a minimum of two years of experience in a directly relevant or demonstrated comparable competency and skill attainment is required. • A Master’s degree in a relevant field may be substituted for the bachelor’s degree and experience., • Authorization to work in the United States indefinitely without restriction or sponsorship. Additional Information Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance of San Diego, CA are encouraged to apply. Pay range is $27.5/h to $32.5/h depending on experience. Excellent full time benefits including • Comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match, • Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionJob Title: Biochemist Location: San Diego, CA Duration: 6 Months Job Summary opening for a self-motivated individual with production experience in a fast-moving and dynamic environment to join our purification team! The Biochemist I will be an integral member of a team that manufactures and provides purified antibodies to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team leader and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will perform antibody purification via column chromatography both manually and automatically, troubleshoot problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. Essential Functions Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. " Follow and understand SOPs and batch records, complying with ISO policies and procedures " Expected to be proficient in purification of monoclonal, polyclonal, and recombinant antibodies both manually and automatically " Perform all essential functions related to antibody purification, including but not limited to the following: procuring appropriate reagents and tools, dilution, endotoxin testing, concentration, and buffer exchange of antibodies " Possess both a basic understanding of antibody protein structures and how antibody purification is performed. " Perform basic math calculations to calculate the amount of antibodies, concentrations, dilutions, etc. " Capable of using lab equipment including but not limited to: AKTA(s), analytical balance, centrifuge, spectrophotometer, nanodrop, UV detector, chart recorder, biosafety cabinet, and pH Meter. Capable of working on multiple projects simultaneously both individually and in a team environment. " Assist in troubleshooting discussions. " Other responsibilities as assigned. Skills: Read and understand SOP's related to antibody purification processes Utilizing Basic Lab Equipment including, but not limited to: AKTA(s), analytical balance, centrifuge, spectrophotometer, nanodrop, UV detector, chart recorder, biosafety cabinet, and pH Meter. Education: Minimum Qualifications Education and Experience " Associate s degree in biology, biochemistry, chemistry, or other related area, biotech certification, or equivalent work experience. " Minimum of 1 year of relevant lab experience with column chromatography, analytical assays, and detection methods in a manufacturing setting or full-time academic environment. Preferred Qualifications Education and Experience " Bachelor s of science degree in biology, biochemistry, chemistry, or other related area, biotech certification, or equivalent experience. " Familiarity with ERP/MRP databases to execute production orders. " Experience working with aseptic technique in biosafety cabinet, basic protein purification, analytical assays such as endotoxin testing, SDS page, IEF, and SEC. " Ability to perform column chromatography and the ability to use lab equipment such as AKTA, various sizes of columns, balance, pipette, spectrophotometer, Nanodrop, UV detector, agarose gel electrophoresis, endotoxin (LAL) tests, and pH meter. " Ability to meet important deadlines and due dates. " Strong multitasking/prioritization skills. " Strong oral and written communication skills.

Job Description About Tr1X Tr1X is a clinical-stage biotechnology company developing engineered Tr1 cell therapies to restore immune balance in autoimmune and inflammatory diseases. Leveraging the unique biology of Tr1 cells, the company is advancing a pipeline of off-the-shelf allogeneic and in vivo CAR-Tr1 therapies designed to deliver targeted immunoregulation and address diseases driven by immune dysfunction, including transplant-related complications. Founded by pioneers in the discovery of Tr1 cells, Tr1X, Inc. is focused on developing durable, potentially curative therapies for conditions with high unmet need. For more information, visit www.tr1x.bio. Position Summary The Director, Medical and Regulatory Writing reports to the Vice President, Head of Regulatory Affairs and provides strategic planning, development, review, and delivery of high-quality medical, clinical, and regulatory documentation supporting Tr1X clinical programs. The role is responsible for establishing and executing medical writing strategies across clinical development programs, ensuring the timely preparation of scientifically accurate, regulatory-compliant documentation. The Director drives document quality and operational excellence and collaborates with senior leaders across Clinical Development, Regulatory Affairs, Biostatistics, Clinical Operations, Translational Medicine, CMC/Technical Operations, and other functions. The position plays a critical role in supporting regulatory milestones and submissions throughout the product lifecycle, while ensuring alignment with applicable regulatory requirements, scientific standards, and corporate objectives. Key Responsibilities • Partner with Regulatory to develop and implement the medical writing strategy in alignment with corporate objectives, clinical development plans, regulatory strategies, and program goals., • Author (writes & edits) high-quality documents across all program areas as needed such as clinical study protocols, protocol amendments, ICFs, clinical study reports, DSURs, Investigator's Brochures, as well as more complex documents, e.g., INDs, NDAs, briefing packages, etc., • Prepare and perform a quality review of clinical study protocols, protocol amendments, clinical study reports, investigator brochures, clinical summaries, and other essential clinical development documents., • Lead, manage, and coordinate process for preparation of documents. This includes leading adjudication meetings to align on scope and to resolve comments, as well as driving timelines and interacting with Regulatory to coordinate final delivery for publishing., • Ensure scientific conclusions are evidence-based, appropriately supported by clinical data, and consistent across the clinical and regulatory documentation portfolio., • Establish standards for document consistency, reference verification, data presentation, medical terminology, and scientific interpretation., • Advise leadership and cross-functional teams on document strategy, content risks, submission readiness, resource constraints, and critical timelines., • Establish medical writing standards, processes, governance frameworks, templates, and quality-control procedures across development programs., • Drive continuous improvement initiatives to enhance document quality, operational efficiency, consistency, timeliness, and compliance., • Ensure compliance with applicable regulatory requirements and guidance, including ICH guidelines, Good Clinical Practice (GCP), and relevant FDA regulatory expectations., • Oversee implementation of quality assurance processes for medical writing deliverables, including content review, document QC, traceability, and controlled document management., • Partner with Quality Assurance and Regulatory Affairs to support inspections, audits, submission readiness assessments, and corrective and preventive actions when required., • Partner with senior leaders and cross-functional team members in Clinical Development, Clinical Operations, Translational Medicine, CMC, and Quality., • Resolve complex content disagreements and drive timely decisions across multidisciplinary teams., • Evaluate appropriate technologies, automation, and artificial intelligence-enabled writing tools while maintaining scientific oversight, confidentiality, data integrity, and regulatory compliance., • Perform other responsibilities based on business needs. Required Qualifications & Experience • Bachelor's degree in a relevant scientific discipline, such as life sciences, biomedical sciences, or a related scientific field and a minimum 10 years of closely related experience. An advanced degree in a relevant scientific discipline preferred., • Experience working in pharmaceutical, biotechnology, or contract research organizations; experience in both sponsor and CRO environments is advantageous; experience on the sponsor side required., • Proven expertise in advanced medical and regulatory writing., • Extensive knowledge of clinical development processes, clinical trial methodologies, regulatory submission requirements, and regulatory authority expectations., • Must have strong knowledge of ICH M11 and principles of the Common Protocol Template (CPT)., • Experience with preparing global protocols and ICFs for studies in multiple regions (e.g. US, EU, UK, Japan), • A successful track record of delivering high-quality medical and regulatory documentation within defined timelines and quality standards., • Knowledge of regulatory guidelines and standards., • Detail-oriented with excellent scientific judgment and ability to apply critical thinking to document preparation and review., • Strong interpersonal, organizational, project management, and verbal and written communication skills., • Advanced computer skills in Microsoft Office 365 programs. Other Requirements • Legally authorized to work for any employer in the U.S., • Position is on-site in San Diego, CA The job responsibilities and requirements provided above are intended to describe the general nature of the work performed by individuals assigned to this job classification. It is not intended to be an exhaustive list of all duties and requirements. Tr1X retains the right to add, change, or delete duties, education, experience or any other requirements of the position at any time. Working at Tr1X At Tr1X, our team is united by a singular shared mission: to transform patients' lives through breakthrough science. We are a group of skilled experts driven by urgency, innovation and a collaborative spirit. Our culture thrives on excellence, positivity, persistence and the agility to tackle new challenges head-on. With an unwavering commitment to patients, science and one another, we foster an environment where team members feel engaged, supported and empowered to make a meaningful impact. We envision a world where autoimmune diseases are not just being treated but are cured. Base Pay Range Anticipated: $200,000 - $220,000 Tr1X considers a variety of factors to determine salary such as education, years of experience, time in the position level, training, knowledge, skills, geographic location, and the market value of the position. Compensation and Benefits Tr1X provides a fair and competitive total rewards program that includes base salary; discretionary annual target bonus; incentive stock options; 401(k) retirement plan with company contribution; health and welfare insurance plans for employees (and their families) that include medical, dental, vision, long-term and short-term disability, and life insurance; paid time off (PTO); and paid holidays. Tr1X embraces a diverse, open, and inclusive environment and believes a strong culture connection is key to success. Tr1X is committed to fairness in recruitment, hiring, transfer, promotion or any other employment practice without regard to race, color, citizenship, national origin, ancestry, religion, sex, pregnancy, marital status, sexual orientation, gender, gender identity and expression, age, physical and medical disability, medical condition, genetic information, political affiliation, protected veteran status, or any other characteristic protected by law. If you are an individual needing assistance to complete an employment application or would like to request an accommodation, please contact the Human Resources department at careers@tr1x.bio. Notice to Employment Agencies The Tr1X talent acquisition program is managed through internal resources, and unsolicited referrals and resumes are not accepted from employment agencies, unless advance written authorization is granted from the human resources department. Tr1X shall not be liable for any fees arising from any unsolicited or unauthorized candidate information received relative to position vacancies.

Job Description CorDx Inc. is seeking an experienced Regulatory Affairs Manager to support the development, registration, and lifecycle management of in vitro diagnostic (IVD) medical devices in the United States. The Regulatory Affairs Manager will lead regulatory strategy and submissions for diagnostic products, including FDA 510(k), CLIA categorization/waiver activities, and other applicable regulatory pathways. The position will work closely with R&D, Clinical Affairs, Quality, Manufacturing, Product Management, and external partners throughout the product development lifecycle. The ideal candidate has at least five years of regulatory affairs experience in the IVD or medical device industry, with hands-on experience preparing FDA submissions and interacting with FDA. Company: CorDx Inc. Location: San Diego, CA Department: Regulatory Affairs / Compliance Employment Type: Full-Time Regulatory Strategy & Product Development • Develop and execute U.S. regulatory strategies for new and existing IVD products., • Determine appropriate regulatory pathways, product classification, predicate devices, and submission requirements., • Provide regulatory guidance to R&D, Clinical, Quality, Manufacturing, and Product teams throughout product development., • Participate in design and development activities and provide regulatory input regarding intended use, indications for use, labeling, performance requirements, and regulatory testing., • Conduct regulatory assessments for product changes and determine whether new regulatory submissions or notifications are required.FDA Submissions, • Lead preparation, review, and submission of FDA regulatory applications, including:, • 510(k) Premarket Notifications, • CLIA Categorization and CLIA Waiver submissions, • Q-Submissions / Pre-Submissions, • Additional Information (AI) responses, • Other FDA submissions and regulatory correspondence as applicable, • Prepare and review regulatory submission sections covering device description, labeling, analytical performance, clinical performance, software, usability, risk management, and other applicable areas., • Coordinate cross-functional submission activities and ensure submission documents are complete, consistent, accurate, and submitted according to project timelines., • Manage FDA submission timelines, commitments, questions, and responses., • Serve as a regulatory point of contact for communications with FDA reviewers., • Participate in FDA meetings, teleconferences, and interactive reviews., • Coordinate and prepare responses to FDA deficiencies and requests for additional information.IVD Performance & Clinical Regulatory Support, • Provide regulatory guidance for analytical and clinical study strategies supporting IVD submissions., • Review analytical performance protocols and reports, including studies such as:, • Limit of Detection (LoD), • Inclusivity and cross-reactivity, • Interference, • Precision and reproducibility, • Stability, • Flex studies, • Method comparison, • Clinical performance studies, • Work closely with Clinical Affairs to ensure clinical study designs and resulting data meet FDA submission requirements., • Review clinical performance results, including PPA, NPA, confidence intervals, invalid rates, and other applicable performance measures., • Support regulatory strategies for POC and OTC diagnostic products and CLIA Waiver applications.Labeling & Lifecycle Management, • Review and approve regulatory aspects of:, • Instructions for Use (IFU), • Package labeling, • Quick Reference Instructions, • Product claims, • Marketing and promotional materials, • Ensure product claims and labeling remain consistent with FDA-cleared intended use and indications., • Maintain regulatory documentation and submission records., • Support post-clearance product changes and regulatory impact assessments., • Monitor relevant FDA regulations, guidance documents, standards, and industry developments affecting CorDx products.Cross-Functional & Compliance Support, • Partner with Quality Assurance to maintain compliance with applicable FDA Quality System requirements and internal procedures., • Participate in design reviews, risk management activities, CAPA investigations, and change control activities when regulatory input is required., • Support FDA inspections and other regulatory audits., • Develop and maintain regulatory SOPs, work instructions, templates, and regulatory tracking systems., • Provide regulatory training and guidance to internal teams., • Mentor junior Regulatory Affairs staff and support development of the regulatory team. Requirements • Bachelor’s degree or higher in Biology, Chemistry, Biomedical Engineering, Clinical Laboratory Science, Regulatory Science, Life Sciences, or a related scientific discipline., • Minimum 5 years of Regulatory Affairs experience in the IVD, medical device, diagnostics, or related regulated healthcare industry., • Hands-on experience preparing and supporting FDA regulatory submissions., • Strong knowledge of FDA medical device and IVD regulatory requirements., • Experience reviewing technical documentation, analytical performance studies, clinical performance data, and product labeling., • Demonstrated ability to manage regulatory projects independently and work effectively across multiple functions., • Excellent technical writing, analytical, organizational, and communication skills., • Ability to manage multiple regulatory projects and deadlines simultaneously.Strongly Preferred, • Direct experience with IVD products and FDA 510(k) submissions., • Experience serving as the primary or key regulatory contact during FDA review., • Experience preparing FDA Additional Information responses and participating in interactive review., • Experience with CLIA Waiver and/or CLIA Categorization submissions., • Experience with point-of-care (POC) and/or over-the-counter (OTC) IVD products., • Experience with infectious disease, respiratory, toxicology, reproductive health, or rapid diagnostic products., • Experience with FDA Q-Submissions/Pre-Submissions., • Experience with De Novo submissions is a plus., • Familiarity with ISO 13485, ISO 14971, design controls, and applicable FDA Quality System requirements., • RAC certification is a plus.Key Competencies, • Regulatory strategy, • FDA submission leadership, • Technical and regulatory writing, • Analytical and clinical data interpretation, • Cross-functional leadership, • FDA communication and negotiation, • Strong scientific judgment, • Attention to detail, • Project management, • Ability to work effectively in a fast-paced diagnostic product development environment Benefits • Comprehensive medical insurance., • 401(k) plan with generous company contributions., • Flexible paid time off (PTO) policy. Equal Opportunity Statement: We are an equal opportunity employer committed to inclusion and diversity. We do not discriminate based on race, gender, religion, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any other protected characteristic.

Job Description About Tr1X Tr1X is a clinical-stage biotechnology company developing engineered Tr1 cell therapies to restore immune balance in autoimmune and inflammatory diseases. Leveraging the unique biology of Tr1 cells, the company is advancing a pipeline of off-the-shelf allogeneic and in vivo CAR-Tr1 therapies designed to deliver targeted immunoregulation and address diseases driven by immune dysfunction, including transplant-related complications. Founded by pioneers in the discovery of Tr1 cells, Tr1X, Inc. is focused on developing durable, potentially curative therapies for conditions with high unmet need. For more information, visit www.tr1x.bio. Position Summary The Research Associate II (RA II) performs a variety of lab responsibilities in support of translational assay development and clinical sample analysis for ongoing and upcoming clinical trials. The RA II possesses a general technical understanding and foundation, strong work discipline, exceptional attention to detail, and the ability to apply critical thinking to generate reproducible, high-quality data that inform the translational development of Tr1X's cell therapy programs. The RA II is expected to operate with a level of general knowledge and independence but will perform duties with oversight and guidance from Translational scientists. This role involves hands-on work with human blood and tissue specimens. Key Responsibilities Assay Development and Clinical Sample Processing • Process human blood and tissue samples according to SOPs and established workflows., • Perform weekly flow cytometry runs, including sample preparation, instrument setup (QC, compensation, PMT adjustments), data acquisition, and troubleshooting., • Complete and deliver real-time data analysis, ensuring accuracy, reproducibility, and adherence to assay requirements., • Conduct MSD/ELISA and molecular assays (e.g., dPCR) as needed., • Maintain cell cultures and perform cell-based assays., • Support assay development, optimization, qualification, and troubleshooting in collaboration with scientists., • Prepare concise summaries of experimental design and results; deliver presentations in team settings., • Ensure accurate, real-time documentation of all activities using an electronic lab notebook (ELN)., • Learn, develop and enhance lab skills, troubleshooting capabilities, and knowledge through scientific curiosity and support from more senior level scientists. Supportive Translational Responsibilities • Contribute to SOP drafting, updates, method documentation, and controlled form revisions., • Participate in clinical sample management including receipt, logging, storage, aliquoting, and preparation for downstream analyses., • Maintain detailed documentation, chain-of-custody, and compliance expectations for clinical samples., • Perform routine lab upkeep such as reagent inventory., • Perform other responsibilities based on business needs. Required Qualifications & Experience • Bachelor's degree in immunology, cell biology or a related scientific field., • Minimum 2+ years of industry or equivalent experience in assay development, immunology, cell biology, or a related field, ideally within a translational or biomarker-focused setting., • Hands-on experience with flow cytometry–based assays, including sample processing, instrument setup, data acquisition, data analysis, and troubleshooting; experience with panel design is a plus., • Hands-on experience in maintaining cell cultures on primary human cells., • Experience executing cell-based assays, such as mixed lymphocyte reactions (MLRs), is a plus., • Demonstrated ability to reproducibly conduct multiplex immunoassays (e.g., ELISA, MSD) and/or molecular assays., • Proficiency with analytical software programs (Prism, FlowJo, etc.)., • Strong attention to detail with the ability to follow SOPs and maintain real-time, accurate documentation in ELNs., • Familiarity with assay development, qualification, and validation workflows, and knowledge of GxP principles or compliance expectations relevant to clinical sample handling and processing, is a plus., • Ability to prepare clear experimental summaries (design and data)., • Ability to manage multiple tasks and meet project timelines., • Thrive in a fast-paced start-up environment., • Agile, flexible mindset with strong organizational skills., • Must be able to wear all required PPE and safely conduct experiments. Other Requirements • Legally authorized to work for any employer in the U.S., • Position is on-site in San Diego, CA. The job responsibilities and requirements provided above are intended to describe the general nature of the work performed by individuals assigned to this job classification. It is not intended to be an exhaustive list of all duties and requirements. Tr1X retains the right to add, change, or delete duties, education, experience or any other requirements of the position at any time. Working at Tr1X At Tr1X, our team is united by a singular shared mission: to transform patients' lives through breakthrough science. We are a group of skilled experts driven by urgency, innovation and a collaborative spirit. Our culture thrives on excellence, positivity, persistence and the agility to tackle new challenges head-on. With an unwavering commitment to patients, science and one another, we foster an environment where team members feel engaged, supported and empowered to make a meaningful impact. We envision a world where autoimmune diseases are not just being treated but are cured. Base Pay Hiring Range Anticipated: $88,000 - $93,000 Tr1X considers a variety of factors to determine salary such as education, years of experience, time in the position level, training, knowledge, skills, geographic location, and the market value of the position. Compensation and Benefits Tr1X provides a fair and competitive total rewards program that includes base salary; discretionary annual target bonus; incentive stock options; 401(k) retirement plan with company contribution; health and welfare insurance plans for employees (and their families) that include medical, dental, vision, long-term and short-term disability, and life insurance; paid time off (PTO); and paid holidays. Tr1X embraces a diverse, open, and inclusive environment and believes a strong culture connection is key to success. Tr1X is committed to fairness in recruitment, hiring, transfer, promotion or any other employment practice without regard to race, color, citizenship, national origin, ancestry, religion, sex, pregnancy, marital status, sexual orientation, gender, gender identity and expression, age, physical and medical disability, medical condition, genetic information, political affiliation, protected veteran status, or any other characteristic protected by law. If you are an individual needing assistance to complete an employment application or would like to request an accommodation, please contact the Human Resources department at careers@tr1x.bio. Notice to Employment Agencies The Tr1X talent acquisition program is managed through internal resources, and unsolicited referrals and resumes are not accepted from employment agencies, unless advance written authorization is granted from the Human Resources department. Tr1X shall not be liable for any fees arising from any unsolicited or unauthorized candidate information received relative to position vacancies.

Job Description Fate Therapeutics is looking for a Senior Manager, Biomarker Operations to help advance innovative clinical programs by shaping and executing biomarker sample strategies across studies. This is an exciting opportunity for a collaborative, detail-oriented operations professional who enjoys partnering across scientific, clinical, and vendor teams, solving complex challenges, and improving processes that support high-quality study execution. This is a full-time, exempt position located at our corporate headquarters in San Diego, CA. Responsibilities • Lead day-to-day biomarker sample operations for clinical studies, including sample logistics, issue resolution, protocol amendments, lab manual updates, study initiation materials, and escalation of study-related risks., • Partner with Translational and Clinical teams to design and implement innovative, feasible biospecimen collection and handling approaches that uphold quality, ethical, and informed consent standards., • Maintain accurate sample inventories and oversee short- and long-term sample storage solutions., • Collaborate with cross-functional stakeholders, including Translational Scientists, Medical Monitors, Clinical Operations, Finance, Procurement, Legal, Data Management, and Quality Assurance., • Work with Quality Assurance to support vendor qualification and audit activities., • Manage CROs and external laboratories to ensure key deliverables, timelines, sample processing, testing, and data reporting meet study specifications and business requirements., • Organize and facilitate meetings with internal and external stakeholders to support alignment and timely execution., • Oversee central lab budgets, contracts, MSAs, legal agreements, and other agreements related to clinical biomarker activities, laboratories, and partnerships., • Coordinate with Clinical and IT teams to manage data reporting from CROs into Fate and clinical study vendor systems, as appropriate., • Provide cross-functional study updates to clinical study and biomarker teams, including sample collection, assay status, and analysis updates., • Develop and update SOPs for cross-functional biomarker operational processes.Qualifications, • MS or higher degree with 3+ years of experience in biomarker operations, or BS degree with 5+ years of relevant experience., • Demonstrated experience managing clinical or biomarker operations from study initiation through completion, including collaboration with central labs and CROs to execute biomarker study plans., • Experience working with clinical trial sites and related clinical CROs., • Knowledge of cancer biology, immunology, biomarkers, drug development, and clinical trial methodology is a plus., • Experience with one or more Laboratory Information Management Systems (LIMS) is strongly preferred., • Prior experience or familiarity with IND preparation and filing is preferred., • Strong planning, organization, and follow-through, with the ability to manage multiple high-priority projects and competing deadlines in a dynamic environment., • Excellent interpersonal, verbal, written communication, presentation, and influencing skills., • High emotional intelligence and a collaborative approach to working effectively across cross-functional teams., • Innovative mindset with the ability to introduce new ideas, improve processes, and solve problems creatively., • Flexibility in schedule and willingness to travel as needed.Working Conditions & Physical Requirements, • Travel may be required (up to 10%)., • Subject to extended periods of sitting and standing, vision to monitor, and moderate noise levels.Compensation, • The salary offer will be based on a variety of factors, including level, experience, qualifications, internal equity, and location., • Fate offers a competitive employment package that includes an annual bonus, equity, and a generous benefits package., • The anticipated salary range for this role is $150,000 - $165,000. The preceding job description indicates the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required from time to time. Equal Employment Opportunity Fate Therapeutics, Inc. is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. Privacy Notice To learn about how Fate collects and uses job application information, please visit Fate's online Privacy Notice. About Fate Therapeutics, Inc. Fate Therapeutics is a clinical-stage biopharmaceutical company dedicated to bringing a pipeline of induced pluripotent stem cell (iPSC)-derived cellular immunotherapies to patients. Using its proprietary iPSC product platform, the Company has established a leadership position in creating multiplexed-engineered master iPSC lines and in the manufacture and clinical development of off-the-shelf, iPSC-derived cell products. The Company’s pipeline includes iPSC-derived T-cell and natural killer (NK) cell product candidates, which are selectively designed, incorporate novel synthetic controls of cell function, and are intended to deliver multiple therapeutic mechanisms to patients. Fate Therapeutics is headquartered in San Diego, CA. For more information, please visit www.fatetherapeutics.com. ⚠️ Recruitment Fraud Alert Recently, we have been made aware of unauthorized individuals falsely presenting themselves as Fate Therapeutics employees or recruiters as part of online scams or phishing attempts. Impersonators may use the Fate Therapeutics name and logo, as well as employee names and job titles, to gain a job seeker’s personal or banking information or to request payment as a condition of being considered for a position at the company. Fate Therapeutics and its employees are not involved in these scams. Here are a few things to be aware of to help identify recruitment fraud: - Our Talent Acquisition team only corresponds from our @fatetherapeutics.com domain. - At no stage in our hiring process will we require payment or ask you to make deposits in your bank account. - We will only ask for personal information when applying for a position via our Careers page or thereafter. - At no stage during our hiring process will we ask you to click a link to begin a one-way video interview. - We do not use Google Hangouts, WhatsApp, or other third-party messaging platforms to recruit candidates or conduct interviews. Please exercise caution. If something feels off about your interactions, we encourage you to contact us at careers@fatetherapeutics.com to confirm the authenticity of the message. Your security is important to us, and we appreciate your vigilance. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job Description Deep Science Ventures is seeking an exceptional formulation chemist to join the team of a new venture at the intersection of crop nutrition and weed control. This is a deeply hands-on role: You will take ownership of a critical part of the technology, developing the formulation and coating system required to translate the underlying biology into a scalable, commercially viable agricultural product. You will design the formulation strategy and personally execute experimental work in the lab, taking the technology from early formulation development through to pilot scale. Depending on your experience, leadership ambition and fit with the founding team, the role could develop as Technical Co-Founder (c-suite), with responsibility for the company's broader technical strategy, or as a founding Formulation Chemist/Lead Scientist working alongside the c-suite. The venture is targeting incorporation and spin-out in early Q2 2027, with pre-seed (incorporation) investment and ongoing support from Deep Science Ventures and the Grantham Foundation. The role is full-time and will require an on-site presence in San Diego, California as the company's laboratory capability is established. The Venture A combination of legislation and weed resistance is giving farmers an ever-diminishing herbicide tool kit. Legacy chemical herbicides have been shown to be toxic to human health and the environment. Meanwhile, farmers are spending thousands of dollars per year on inefficient crop nutrition with at best 50% of what is administered benefiting the crop. The remainder is polluting our water systems or feeding weeds that compete with the crop for nutrients. Thus weeds are costing farmers twice - on wasted nutrients and on herbicides. We are building a solution to address this paradox, with a technology that delivers nutrients exclusively to crops. It is designed for compatibility with existing farming practices, thereby enabling large scale impact via both increased nutrient use efficiency for yield and weed starvation to lower herbicide demands. You’ll build the company alongside Dr. James Pearce, an experienced ag-biotech R&D leader with 20+ years spanning startups and global crop-science companies. He has held senior roles including CSO at Boost Biomes and VP Research at CH4 Global, alongside earlier leadership roles at Monsanto/Bayer, Cibus and Syngenta. His experience spans microbial crop inputs, biologicals, field trials, bioprocess scale-up, regulatory and IP strategy, and strategic partnerships. Requirements You’re motivated by ambitious, unsolved challenges and the opportunity to challenge the status quo in agrochemicals. You’re entrepreneurial, impact-driven and comfortable taking initiative in ambiguous, fast-moving environments, using first-principles thinking to figure out what’s really needed. You collaborate with patience and an open mind, and are willing to go where the company needs you most as the venture evolves. Technical Experience: • PhD or equivalent technical depth in Chemistry, Materials Science, Polymer Science, Biochemistry or a related discipline;, • Significant industry R&D experience developing formulations or coatings from bench towards pilot scale;, • Deep expertise in controlled-release formulation/coating systems, ideally involving fertilisers, agricultural inputs or another relevant controlled-release application;, • Hands-on experience with fluid-bed coating or closely analogous coating processes;, • Strong understanding of film properties, coating integrity and dissolution/release kinetics;, • Experience working with biopolymers or polymer modification and characterisation; experience with esterification, degree-of-substitution control, NMR and titration is particularly relevant;, • Experience applying formal Design of Experiments (DoE) to multi-parameter formulation or coating optimisation, using tools such as JMP, Design-Expert, Minitab or R;, • Experience considering scale-up, manufacturability and cost-of-goods alongside technical performance;, • Experience with enzyme-substrate interactions and kinetics, microbial formulations, fertiliser coatings or other biological/chemical interfaces would be particularly valuable. Track record: For candidates interested in taking on the broader Technical Co-Founder (c-suite) role, we're additionally looking for experience in/the ability to: • Set technical strategy and prioritise the experiments that most rapidly de-risk the company;, • Build and lead multidisciplinary R&D teams;, • Make pragmatic decisions about technical risk, resources and capital allocation;, • Own technical elements of fundraising, partnerships and investor diligence;, • Develop and protect the company's IP position;, • Communicate complex science clearly to investors, commercial partners and other non-specialists;, • Operate with the ownership, adaptability and resilience required of a founder. Responsibilities You will own formulation development and help translate the technology from the bench towards a scalable agricultural product. Depending on expertise, you will: • Define the fertiliser formulation and coating strategy and personally execute experimental work at the bench;, • Design and iterate coating systems based on release kinetics, biological performance, manufacturability and cost of goods;, • Take formulations from bench towards pilot scale, identifying the critical technical and scale-up risks along the way;, • Define product specifications that are technically robust and commercially viable;, • Design rigorous experiments and use DoE/data-driven approaches to optimise multi-parameter formulation systems;, • Establish the chemistry capability within a shared laboratory, including selecting equipment, reagents and experimental infrastructure;, • Identify patentable inventions and contribute to the development of the company's IP strategy;, • Represent the technology credibly with external technical partners, investors and the wider Ag Biotech community;, • As the team grows, help recruit, mentor and lead additional technical talent. Benefits The setup The venture spins out with £250k in inception capital from DSV and the Grantham Foundation. The founding team will collectively hold a majority equity stake in the company, and salary is negotiated as part of the spin-out. Post-launch, DSV provides continuous portfolio support - fundraising, partnerships, recruitment. The role is full-time and will require an on-site presence in San Diego, California as the laboratory is established. Candidates must be authorised to work full-time in the US. For an exceptional candidate with the breadth and ambition to join as a Technical Co-Founder, founder-level equity and leadership responsibility will reflect that role. About DSV Deep Science Ventures (DSV) is on a mission to create a future in which both humans and the planet can thrive. We use our unique venture creation process to create, spin-out, and invest in science companies, combining available scientific knowledge and founder-type scientists into high-impact ventures. Operating in four sectors—Pharmaceuticals, Climate, Agriculture, and Computation—we tackle the challenges defining these areas by taking a first principles approach and partnering with leading institutions. About Grantham The Grantham Foundation for the Protection of the Environment was established in 1997 by Jeremy and Hannelore Grantham. Jeremy is co-founder and Chairman of investment management firm GMO, LLC. Jeremy was elected a member of the American Academy of Arts and Sciences in 2015, was appointed Commander of the Order of the British Empire (CBE) in 2016, and received with Hannelore the Carnegie Medal for Philanthropy in 2017, all for leadership in climate change activities.

Job DescriptionAbout Us We are an award-winning California-based environmental consulting firm with 550+ professionals and more than 30 years of diverse experience serving clients in transportation, energy, water, infrastructure, private development, and government sectors. Our mission is to deliver practical, science-based environmental and planning solutions that support communities, infrastructure, and natural systems. As a people-centric organization, we value collaboration, fairness, and transparency, and are committed to fostering a workplace that supports both personal and professional growth while offering robust career opportunities. We are especially proud of our recent Great Place To Work® certification, which reflects an independent assessment of our culture and our team-member experiences. About The Role This leadership role involves managing client relationships, overseeing internal teams, and driving both current programs and new business development in the Energy and Utilities market. The focus will be on either renewable energy or utilities, depending on the candidate’s expertise. The ideal candidate will have significant experience in business development, client management, strategic consulting, QA/QC oversight, and team leadership. This position also involves working closely with Rincon leaders across multiple disciplines and service lines. Strong communication and mentorship skills are essential for success in this role. How We Collaborate While this role may offer flexible work arrangements that can include a mix of in-office and remote work, our changing business needs will ultimately determine our level of remote-work flexibility. Additionally, to promote in-person collaboration and client teaming, we prioritize hiring those who reside within 50 miles of a Rincon office which currently includes: Carlsbad, Fresno, Los Angeles, Monterey, Oakland, Palm Springs, Riverside, Sacramento, San Luis Obispo, San Diego, San Jose, Santa Barbara, and Ventura. What You’ll Do Strategic Business Development and Client Management • Lead the development and oversight of Rincon’s statewide Energy and Utilities market, collaborating with other Rincon leaders, • Manage key client relationships and support renewable energy production and utility projects, • Drive business development, including proposal preparation, client outreach, marketing, and strategic planning for the Energy and Utilities market, • Align business development efforts with other service lines to pursue strategic opportunitiesOperations and Technical Guidance, • Oversee business operations, including contract and risk management, ensuring program efficiency and compliance, • Provide final quality assurance reviews for technical studies and ensure projects meet schedule and budget goals, • Delegate and manage technical assignments to ensure successful project completion, • Guide Rincon’s renewable energy and utilities services, ensuring regulatory compliance and operational excellenceTalent Advancement and Team Leadership, • Recruit and develop qualified staff for renewable energy and utilities programs, • Mentor senior staff on strategic thinking, business development, and program management, • Lead and motivate teams to ensure high performance and productivity, while managing performance reviews and professional developmentWhat You’ll Bring, • Bachelor’s degree in Biology, Environmental Science, Environmental Policy, or a related field, • 15+ years of progressive experience in environmental consulting, including project management, business development, and technical leadership within the energy or utilities sectors, with a focus on overseeing high-stakes projects and driving business growth, • Exceptional communication, presentation, and organizational skills, with expertise in budgeting and client engagement, ensuring successful project delivery and business expansion in the renewable energy and utilities sectors, • Strong business acumen and customer service skills, with active participation in industry organizations and leadership in regulatory and industry standards, • Proven ability to streamline processes and workflows for greater efficiency while managing and building collaborative teams, • Proficiency with digital tools and platforms (e.g., SharePoint), with strong file management, time management, and organizational skills to handle complex projects Investing in You The base salary range for this full-time position is $170,000–$190,000, plus a generous benefits program. Salary ranges are based on the market median of similar jobs, according to third-party salary benchmark surveys. Base pay is determined based on internal equity and a candidate’s job-related knowledge, skills, and experience. We offer a comprehensive Total Rewards Package designed to support employee well-being, growth, and financial security. Our benefits are designed to offer flexibility and choice, including health coverage options, employer-sponsored insurance, retirement benefits, generous time off, and programs that support learning, growth, and community engagement. Explore more about our culture, benefits, and life at Rincon on our Culture and Benefits page. Additional Employment Information Individuals offered employment must successfully complete a pre-employment drug screening as a condition of employment. Additionally, those hired who may be assigned to federal projects will be subject to further drug testing, including screening for cannabinoids (THC/marijuana), in compliance with the Drug-Free Workplace Act of 1988 and other applicable federal regulations, which take precedence over California state and local laws. Rincon Consultants does not accept unsolicited applicant/candidate resumes from search firm recruiters and/or temporary agencies that do not have a signed contract and specified work order with Rincon Consultants. Further, such resumes received will be deemed the sole property of Rincon Consultants and no fees will be paid in the event Rincon Consultants subsequently hires such individual. Rincon Consultants is an equal opportunity employer. All aspects of employment will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. Powered by JazzHR DJIQ7j9NK2