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Job Description QC Analyst – Microbiology (Contract) – BioPhaseLocation: San Diego, CA Assignment: 4-month contract Pay: $33–35/hr Schedule: Monday–Friday, 8:00 am – 5:30 pmAbout the RoleOur 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 About Us Pluslife is an innovative biotechnology company specializing in advanced diagnostic solutions for both human and veterinary healthcare. As a fast-growing pioneer in molecular and rapid diagnostic technologies, we are committed to delivering accurate, accessible, and reliable testing products that empower healthcare professionals, laboratories, and consumers worldwide. Our mission is to advance global health through scientific excellence, technological innovation, and high-quality diagnostic solutions. The company has received multiple honors, including Leading Entrepreneurial Talent and Team, Specialized and Innovative SME, High-Tech Enterprise, and the 2024 Healthcare CSR Model Enterprise. Powered by proprietary RHAM technology, Pluslife has developed molecular POCT devices and test cards for major infectious diseases, respiratory and reproductive tract infections, and pathogens in companion animals. We have filed over 170 patent and certification applications, with more than 50 granted and 120 approved internationally. Our products are used across countries and regions worldwide. About the Role We are seeking an experienced and driven Veterinary Business Development Manager to expand our animal health market presence and grow our veterinary diagnostic product line. The ideal candidate has strong client resources, established relationships with distributors, veterinary hospitals, clinics, laboratories, and experience building a profitable sales pipeline in the veterinary industry. This role requires deep understanding of the veterinary market, including USDA regulatory requirements, contract manufacturing organizations (CMO), and commercialization of animal diagnostic products. You will play a critical role in expanding channel partnerships, driving revenue growth, and strengthening our position in the Veterinary IVD market. Key ResponsibilitiesBusiness Development & Sales Expansion • Identify, engage, and develop new business opportunities within the veterinary diagnostic market., • Build and maintain relationships with distributors, wholesalers, veterinary clinics, reference labs, and industry partners., • Leverage existing client resources and networks to accelerate market penetration., • Develop, manage, and expand a high-quality sales pipeline across multiple veterinary product lines., • Achieve and exceed quarterly/annual revenue targets. Channel & Distributor Management, • Establish and manage distributor partnerships across domestic and international markets., • Conduct distributor training, performance reviews, and sales enablement activities., • Negotiate commercial agreements, pricing models, and partnership terms. Veterinary Product Knowledge & Technical Guidance, • Promote and communicate the value of veterinary diagnostic products including rapid tests, molecular assays, and laboratory solutions., • Provide product training, demonstrations, and technical presentations to key accounts and distributors., • Act as a subject-matter liaison between customers and internal R&D, regulatory, and product teams. Regulatory & Industry Understanding, • Maintain working knowledge of USDA regulations related to veterinary diagnostic approvals and compliance., • Collaborate with regulatory and CMO partners to ensure product readiness, certification, and market acceptance., • Understand regulatory pathways and quality requirements for veterinary IVD manufacturing and distribution. Market Intelligence & Strategy, • Conduct market research to identify trends, competitor activities, and new market opportunities., • Provide insights to support product strategy, pricing, and go-to-market approaches., • Work cross-functionally with marketing, product management, and operations to drive strategic initiatives. Events & Customer Engagement, • Represent the company at veterinary conferences, trade shows, and industry events., • Bachelor’s degree in Animal Science, Veterinary Science, Biology, Business, or related field., • 3–7 years of experience in veterinary product sales, business development, or animal health industry., • Existing client resources such as distributor network, veterinary clinic relationships, or channel partners., • Proven success in building and managing sales pipelines., • Strong understanding of veterinary diagnostic products (IVD, rapid tests, PCR, analyzers)., • Experience working with USDA regulatory processes for veterinary products., • Strong communication, negotiation, and presentation skills., • Ability to travel domestically., • Experience working with CMOs (Contract Manufacturing Organizations) in animal health., • Knowledge of animal health market segmentation (companion animal, livestock, equine, poultry)., • Experience selling to veterinary distributors, key opinion leaders (KOLs), and corporate veterinary groups.

Job Description Attending Veterinarian, Laboratory Animal Medicine. The Attending Veterinarian is responsible for ensuring the clinical care of animals on all studies in the vivarium as well as colony animals. In addition, the individual would oversee surgical procedures, post-operative care, and diagnostic imaging while overseeing the team of veterinary staff. The Attending Clinical Veterinarian will contribute to the team by: * Providing medical and surgical care for laboratory animals to ensure adequate and humane veterinary support * Performing physical, ophthalmic, and other needed exams on laboratory animals * Providing expertise on anima health, biology, physiology, and research methodology to staff scientists and technicians, and providing training to staff when necessary. * Providing expertise on research studies and becoming involved as a partial Study Director for preclinical research studies. Principal Duties and Responsibilities * Manage the clinical care of all laboratory animals on site. * Manage and provide direction to junior staff, scheduling activities, and personnel development of the veterinary technical team. * Develop and revise SOPs to assure facility compliance with applicable regulations, client expectations, and current industry standards. * Assisting the site supervisor to ensure that the policies and practices regarding animal care and welfare are in compliance and contain relevant regulations * Reporting all animal care concerns and becoming involved in the resolution. * Ensure the facility is in compliance with all applicable guidelines, regulations, and standards that relate to animal care and use as it pertains to USDA, FDA, and AAALAC * Direct, implement and oversee health monitoring, developing, and implementing corrective actions for deficiencies and technical oversight of veterinary staff. * Deliver and develop clinical training programs for the veterinary and research staff. * Provide clinical and technical support to internal and external customers * Provide anesthesia and perform surgical support along with surgical and analgesic technical expertise to facilitate protocol development. * Ensure adherence to established protocols and help to refine best practices * Participate in inspections both internal and external with clients * Provide support for activities for the IACUC (Institutional Animal Care and Use Committee) including protocol development, review, and facility inspections along with serving on the IACUC committee. Education: * -Veterinary Degree (DVM or VMD) from a US accredited veterinary program or foreign veterinary program with requirements met for US state licensure * -Experience in Laboratory Animal Medicine * -Ability to gain a Califonia DVM license or commitment to obtain with 60 days of an offer. Benefits include: * DEA registration reimbursement * Continuing education reimbursement * Assistance and encouragement for DACLAM certification * Paid time off * Paid Holidays * Medical, Dental, and Vision Insurance * 401K

Company Description OHR uses primordial chemistry and synthetic biology to fashion strategic chemicals. Our technology enables the creation of carbon chains of deterministic length without cells, co-factors, or typical oil contaminants. With a core value of sustainability, OHR is focused on building resilient supply chains through innovative solutions. Role Description OHR Synbiosis seeks a highly experienced Chemistry Director or Sr. Principal Scientist to lead technical developments and technology transfer across R&D groups and between the broader OHR organization. The candidate will lead development of synthetic chemistry routes of OHR’s Creationary ChemistryTM platform, including: organic chemistry synthetic pathway exploration and discovery, reaction process optimization, catalyst development, analytical methodologies, product application, and external technical partnership management. Responsibilities • Exemplify excellence in lab safety and chemical hygiene practices., • Direct research and development on OHR’s Creationary ChemistryTM platform across multiple physical locations. Lead the drive to deliver critical chemicals to public and private customers in need., • Oversee discovery of organic and synthetic chemistry reactions to create novel synthetic routes leveraging OHR’s proprietary enzymatic intermediates., • Guide chemical reaction development across product pathways, including solvent selection, catalyst elucidation/optimization, reaction conditions, etc., • Lead Process Chemistry R&D to design, optimize, and scale catalytic processes, including acid/base catalysis, heterogenous supported-metal and inorganic catalysis, hydrogenation, and hydrodeoxygenation., • Oversee development of analytical methodologies, in-house and with partners, to build quantitative standing of chemical reactions., • Build testing and characterization protocols for OHR’s aviation and aerospace fuel product portfolio and additional proprietary emerging product portfolios., • Design, test, validate, and find partners to scale novel heterogenous inorganic catalysts., • Develop long-term research and IP strategies to solidify the Creationary ChemistryTM platform., • Recruit, hire, and build additional talent to strengthen OHR’s chemistry group., • Oversee technology transfer to OHR’s Manufacturing team and external partners., • With Project Managers and Executives, implement project managements systems to track Chemistry R&D developments and KPIs. Required Qualifications • Doctoral Degree in Chemistry, or equivalent area, from an accredited university., • Previous Director level experience > 1 year., • Exemplary past demonstration of lab and workplace safety., • Direct experience simultaneously leading and guiding multiple technical chemistry research and development teams., • Direct experience overseeing discovery and development of synthetic chemistry pathways., • Direct experience overseeing process chemistry and reaction optimization teams., • Direct experience exploring and selecting or synthesizing and evaluating heterogenous metal catalysts for hydrogenation and reduction chemistry., • Direct experience discovering or optimizing acid and based catalyzed reactions., • Direct experience managing development of analytical methods of compound identification and quantification, including utilization of GC-FID, HPLC, LC/MS, GC/MS, NMR, and ICP., • Experience managing international technical teams or technical partnerships., • Direct hands-on experience converting established batch reactions to flow/continuous reactions., • Past experience hiring, training, and managing younger scientists., • Ability to control ITAR and Export Compliance restricted information.

Yoh Life Sciences is hiring a long term contractor for a Senior Research Associate, Neuroscience / Cell-Based Screening in San Diego, CA. We are seeking a highly motivated Senior Research Associate with strong expertise in cell-based screening and assay development to support drug discovery programs focused on neuronal targets. The ideal candidate will bring hands-on experience with high-throughput and high-content screening, preferably in an industry setting, and will play a key role in assay development, screening execution, and hit-to-lead activities. Title: Sr. Research Associate Location: San Diego proper Pay: $34-40/hr DOE Schedule: M-F 9-5pm Duration: contract with ability to convert to perm Key Responsibilities • Design, develop, and execute primary high-throughput screening (HTS) assays, • Optimize and run counter-screens and SAR assays to triage and characterize hits from primary screening campaigns, • Analyze, interpret, and clearly present experimental data to project teams, • Collaborate closely with medicinal chemistry, biology, and pharmacology teams to advance programs, • Maintain detailed experimental documentation and ensure high scientific rigor and reproducibilityQualifications, • Bachelor’s or Master’s degree in Biology, Neuroscience, Pharmacology, or a related discipline, • Cell-based screening experience, including high-throughput and/or high-content screening, ideally in an industry setting, • Experience with neuronal cell culture, with preference for human stem cell–derived NPCs and neurons, • Proficient in immunofluorescence, • Hands-on experience with assay development and optimization, • Familiarity with automated liquid handling and screening platforms, • Strong data analysis, troubleshooting, and experimental design skills, • Ability to work independently while contributing effectively within cross-functional teamsPreferred Skills, • Experience with flow cytometry, • Exposure to drug discovery workflows, including HTS, SAR, and lead optimization, • Comfort working in a fast-paced, collaborative research environment #IND-SPG Estimated Min Rate: $34.00 Estimated Max Rate: $40.00 What’s In It for You? We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include: • Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week), • Health Savings Account (HSA) (for employees working 20+ hours per week), • Life & Disability Insurance (for employees working 20+ hours per week), • MetLife Voluntary Benefits, • Employee Assistance Program (EAP), • 401K Retirement Savings Plan, • Direct Deposit & weekly epayroll, • Referral Bonus Programs Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. 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. Visit to contact us if you are an individual with a disability and require accommodation in the application process. For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment. 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. By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice:

Local Candidates Only San Diego, California, United States • We are seeking a highly motivated and organized Scientist II to contribute to the research and development of monoclonal antibodies in our Antibody Technologies team., • This individual will be responsible for working in a dynamic team environment and be a contributor to multiple work streams, including but not limited to protein expression and purification; tissue culture and cell-line engineering; and testing antibodies for use in flow cytometry application. EDUCATION AND EXPERIENCE • A Bachelor’s or Master of Science degree in biochemistry, cellular or molecular biology, immunology, or related discipline., • Minimum of 2-4 years of laboratory experience required. Protein purification, protein expression, molecular biology and tissue culture experience required.

Job Description MeBe is a provider of evidence-based therapies for children with autism and other special needs. Our mission is to empower families, professionals, and communities by educating and training them on evidence-based approaches. Our secret sauce? Play-filled, research-based care across multi-disciplines including OT, Speech and ABA. At MeBe, you’ll be offered more than a job. You’ll receive training and support to launch a career in Behavior Therapy and grow as an individual. You’ll work with extraordinary team members who share a common goal, to help children with autism be their best selves. Your days will be filled with meaning and purpose. To help you prepare for the role, MeBe offers one of the top ABA training programs using the Vincent Carbone method. MeBe Family will also pair you with Supervisors to shadow, ask questions and guide you. MeBe is growing our team and is on the lookout for empathetic, thoughtful individuals with a genuine passion for working with young children to join our fantastic crew. Whether you are an experienced RBT or curious and want to learn more, we would like to meet you. Behavior Technician - Kearny Mesa About You: * You are a caring, compassionate and empathetic individual who loves to learn. * You possess a strong work ethic and are reliable. * You take pride in your work, pay attention to the small details and have a reputation for doing high quality work. * You value transparency and operate with candor and compassion. You inspire others to be their best selves. * You love to weave fun and laughter into whatever you do. Making a positive impact is what drives you * You value individuality and find yourself gravitating towards people with other interests who think outside the box, and push the status quo. * You embrace the power of teamwork and thrive in both one-on-one and group settings – because you know collaboration is the core of achieving big goals. About What You’ll Work On: Autism spectrum disorder (ASD) is a group of developmental disabilities that can cause significant social, communication, mental health and behavioral challenges. Although autism can be diagnosed at any age, it is described as a “developmental disorder” because symptoms generally appear in the first 2 years of life. People with ASD may face a wide range of issues, which means that there is no single best treatment for ASD. Working closely with a health care provider like MeBe Family is an important part of finding the right combination of treatment and services. (Reference, National Institute of Mental Health) As a Behavior Technician, * You'll teach and nurture behavioral, social, communication, and daily living skills in a 1:1 setting to kiddos with autism in their home or at MeBe’s Learning Center clinic * You’ll follow treatment plans developed by BCBAs that help increase the kiddo's communication, self-help, social and play skills. * You’ll relay info on your kiddos’ progress to BCBAs to keep them informed and assist with BCBA assessments. * At the end of each session, you’ll accurately record the kiddo’s behavior analysis and progress in our data collection system Central Reach using your work assigned tablet. * You’ll be responsible for clocking in, submitting your session notes and clocking out to align with strict ABA and Insurance provider regulations. * You’ll help keep our workplace shipshape, safe, and super organized. * You’ll help our kiddos with lunch breaks, bathroom breaks and diaper changing. * You’ll help with projects and tasks as directed by your Site Director and Clinical Supervisors. * You’ll voice questions, issues and concerns to your supervisors as appropriate and take co-ownership of treatment planning. * You’ll help to build positive relationships with families while maintaining professional boundaries. * You’ll positively contribute to the MeBe Family culture. Qualifications: * Consistent availability from Monday through Friday. Part-time shifts available. * Must be at least 18-years-old with a valid driver's license and reliable transportation. * RBT/ CBT certification preferred. Must obtain RBT/CBT certification within 60 days of employment (MeBe will help you!) * Prefer a background in child care; teaching, counseling, babysitting. * Ability to frequently bend, lift (up to 50 lbs), squat, sit, stand, and/or run, (without reasonable accommodations), see with prescription lenses, and hear with hearing aids. * Previous training in First Aid Certified and CPR is preferred * Ability to pass a background check. * Ability to work with computers. * If residing in CA, AZ, or VA, must obtain CPR/BLS certification before working with clients * Must have at minimum a high school diploma or equivalent- required. A bachelor’s degree in areas like Pediatrics or Human Development (Biology) is preferred. Perks and Benefits: * Industry benchmarked, competitive pay based on experience and location. * Pay: $22-27/ hour, depending on experience and location * Paid training to become a Registered Behavior Technician (RBT) through the Behavior Analyst Certification Board * Continuing education; MeBe’s Candidate Program for aspiring BCBAs and BCaBAs * Mentoring from lead clinical staff * Paid time off for Full Time BTs. * Medical, Vision, Dental for eligible employees * Life, AD&D, Accident, Hospital Indemnity, Short Term Disability, and Critical Illness Insurance * Invest in your mental health with access to free mental health sessions * Protect your pet with discounted pet insurance * Secure your future with our 401k program * Unlimited employee referral bonuses * Tuition discounts available to all employees through our University Partnerships * Expansive treatment spaces in applicable locations * Company sponsored, fun events for everyone For more information, please visit our website at We are an equal opportunity employer and prohibit discrimination/harassment 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 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 RoleBioPhase 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 Who we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a #MiracleMaker to join our CDMO Commerical team as a Director, Commerical CDMO. As a Director, Commerical CDMO, you will oversee and develop CDMO Services sales and PgM teams. Position is reporting to the VP and GM of Trilink CDMO and this leader will have responsibility for CDMO sales strategies, mRNA service markets and strategic positioning, pricing, customer / program management and forecasting for the TriLink CDMO services business. This leader will evaluate market performance while developing corporate long-range plans, goals, and objectives to strategically increase revenue and CDMO capabilities. This leader will interact with varying levels of internal and external customers as well as our business partners internal to Trilink Global products and services with a team-focused approach for continuous improvement and revenue growth. Strong sales strategies, business acumen, mRNA market awareness, customer focus and mRNA CDMO program experience are essential. How you will make an impact: • Drive sales and program management for CDMO services (Pre IND through to BLA and Commercialization) by identifying, developing, and closing opportunities across biotech, pharma, diagnostics, and life sciences accounts and managing milestones across execution to provide a best in Class Customer experience., • Develop and manage individual(s) as a part of the CDMO Leadership team to achieve defined sales and business objectives across the CDMO Service portfolio., • Build and sustain executive-level relationships with key decision-makers to catalyze the sales process., • Drive the development of new preclinical and clinical service accounts leveraging Trilink CDMO Capabilities including Process Development, Analytical Services and GMP to support the Customer journey from IND though to BLA and Commercialization., • Own Global CDMO strategies, pipeline management, and accurate forecasting through CRM (Salesforce)., • Partner cross-functionally with Maravai / Trilink Global Marketing, Commercial and Product Management to align on account strategies and educational campaigns raising awareness of TriLink's CDMO capabilities., • Develop and implement effective educational campaigns to support expansion of CDMO services awareness pre-GMP, preclinical to GMP and IND, and through Phase 2/3 to BLA and Commercialization, • Represent TriLink at key conferences, symposia, and industry events; stay current on mRNA clinical trends, • Leverage VOC to inform marketing tactics and product development strategy., • Lead management and accuracy of proposals, MSAs, SOWs, and other high-quality client-facing materials., • Meet or exceed revenue and pipeline growth targets., • Develops and maintains tools to effectively review, analyze and expand TriLink CDMO services sales achievements and program execution vs. strategic goals, • Develops and maintains forecasting, analysis and market share attainment for TriLink CDMO services with a deep understanding of market position, costs, pricing and supporting analytics., • Stays current with industry trends and market intelligence, specifically with respect to TriLink's current CDMO services and capabilities, to understand key competitive issues in relation to process, timing, costs, pricing and business strategy, • Responsible for program management and customer satisfaction as we manage contract milestones and Change Orders across programs and CDMO services departments., • Leads with cross-functional stakeholders, including Quality, Legal, Finance, PD / MFG, Supply Chain, R&D, and Eng to execute internal costing, SOW execution and best-in-class customer experience, • Gathers market and competitive intelligence and stays attuned to customer needs / feedback, • Monitors and aligns customer requirements with CDMO capabilities to effectively coordinate and execute on-time program delivery of GMP SOWs., • Develops, communicates, and coordinates improvements in strategy and execution, and provides development for the sales and program management teams to achieve goals, • Provides proactive and in-depth financial analysis to drive sales across CDMO services, • Conducts advanced analysis and business research to report on current and future CDMO services, • Leads strategies for sales promotions, marketing materials, and Maravai / Trilink cross selling, • Needs to be able to work in a fast-paced, multi-tasking environment, • BS in Molecular Biology, Biochemistry, Genomics, or related field (Advanced degree preferred)., • At least 7 to 10 years of relevant work experience in the biopharmaceutical industry, with at least 5 years of sales achievements and customer-facing experience, preferably in a CDMO setting, • Proven ability to sell in complex, multi-stakeholder environments with demonstrable revenue growth achievements and strong indirect leadership capabilities, particularly in influencing and motivating teams to achieve group goals, • Strong people leader with at least 5 years of people management in a commercial related team, • Ability to work independently with 40%+ travel across territories., • Technical background in nucleic acid, gene editing, cell therapy and/ or bioprocessing, • Strong understanding of drug development pathways, GMP manufacturing, and regulatory requirements., • Skilled in Salesforce, MS Office (Word, Excel, PowerPoint); strong presentation and negotiation skills., • Strong communication and presentation skills, • Must demonstrate collaborative work style, with a strong ability to build relationships, gain credibility, and partner with internal customers, • Strong organizational and strategic management skills, • Strong analytic skills in the area of mRNA service programs to provide growth strategies, • Ability to summarize detailed data into an actionable recommendation for a variety of audiences, • Ability to manage multiple projects simultaneously, with great attention to detail #LI-Onsite The benefits of being a #MiracleMaker: • You have the potential to change, improve, and save lives around the world., • You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans., • We offer comprehensive medical plans and HSA/FSA options., • Fertility & family planning assistance., • A variety of additional optional benefits and insurance options, including pet insurance., • Retirement contributions. To view more opportunities to become a #MiracleMaker, visit our career site at Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Click here to view Maravai LifeSciences Privacy Notice HIRING SCAM ALERT Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: • Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.), • Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment., • Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at . If you believe you have been a victim of fraud, you can report this activity at: or .

Job Description Job Description: ADARx is seeking a qualified and highly motivated individual Lab Manager to join the R&D Department. The Lab Manager will provide operational and scientific support for a fast-paced biotechnology research environment to ensure smooth functioning of the lab while maintaining compliance with safety standards. This role is ideal for a highly experienced professional who can operate independently, proactively manage laboratory operations, and ensure the efficient, compliant, and safe execution of research activities. The Lab Manager will serve as a key partner to scientific teams, requiring minimal supervision and a strong ability to anticipate and resolve issues. Essential Responsibilities: • Oversee day-to-day laboratory operations to ensure efficiency, organization, safety, and compliance (e.g., company policies, OSHA, EPA, EHS, local guidelines)., • Oversee proper functioning and maintenance of all laboratory equipment, including calibration, maintenance and repairs., • Serve as a liaison with external vendors and landlord, manage service contracts, and operate as the primary point of contact for lab-related issues, troubleshooting independently when possible., • Manage shipping and receiving of laboratory materials, including reagents, and samples, ensuring proper compliance with company’s policies and IATA shipping certificate., • Oversee inventory management, ordering, and stock levels for reagents, consumables, and supplies; maintain equipment inventory., • Lead lab safety programs, including chemical hygiene, waste disposal, emergency procedures, safety inspections and training., • Support onboarding and training new lab personnel on lab protocols and safety practices., • Implement best practices to support a growing and evolving R&D organization, including establishing, maintaining and improving lab processes, SOPs and workflows., • Manage lab scheduling, space utilization, and shared equipment across Discovery Biology and Discovery Chemistry research teams., • Partner closely with scientists, IT, Legal, and external vendors and act as a trusted operational advisor to internal stakeholders and research leadership., • Identify opportunities to streamline operations, reduce costs, and improve productivity., • Anticipate future lab needs based on scientific and business demands., • Oversee day-to-day laboratory and vivarium operations to ensure efficiency, organization, safety, and compliance (e.g., company policies, OSHA, EPA, EHS, local guidelines)., • Bachelor’s degree in Biology, Chemistry, Biochemistry, or a related scientific field., • Minimum of 5 years of experience managing laboratory operations in a pharmaceutical, biotech, or life sciences environment., • Demonstrated ability to work independently with minimal supervision., • Strong knowledge of laboratory safety, compliance standards, and best practices., • Proven experience managing equipment, vendors, and lab budgets., • Experience supporting discovery and/or development-stage research., • Must be able to work independently with supervision as needed., • Must be collaborative and work well with other team members in a matrix team environment., • Excellent written and verbal communication skills are essential for this role., • Strong organizational skills with attention to detail and accuracy., • Ability to maintain a high level of confidentiality and exercise discretion., • Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges., • Understand project timelines and deliverables and plans/coordinate project work accordingly with departmental, functional, and external stakeholders., • Occasional after-hours availability may be required to respond to critical equipment alarms or other urgent laboratory matters. Reasonable accommodation(s) may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis. On-Site Protocol: Physical presence at the ADARx Pharmaceuticals worksite is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. Compensation: • This is a full-time position, Monday-Friday, • Pay is commensurate with experience, • Equity-based compensation, • Performance-based bonuses, • 401(k) with Company Match, • Medical, Dental, Vision, • Flexible Spending Account, • Life Insurance, • Employee Assistance Program, • Employee Discounts, • Gym Membership, • Paid Vacation, • Paid Holidays, • United States (Required), • Background Check ADARx Pharmaceuticals, Inc., (the “Company” or “ADARx”) located in San Diego, is a late-clinical stage biotechnology company committed to turning cutting-edge science into life-saving therapeutics. ADARx has developed proprietary RNA targeting platforms and technology for silencing or editing target mRNA. ADARx has a growing pipeline of RNA targeting therapeutics for treating diseases across a range of therapeutic areas including genetic, cardiometabolic, complement-mediated diseases and central nervous system. ADARx currently has multiple active programs in development with the lead candidate in the clinic. We are well-financed by a syndicate of highly regarded investors. ADARx Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Disclosure Statement • The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position., • Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations., • The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual target bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, type and length of experience within the industry, and other job-related factors permitted by law., • Total Compensation includes base salary; benefits: medical, vision, and dental insurance; life insurance; 401(k) matching program; paid time off; paid holidays; Employee Assistance Program; and other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including but not limited to cash bonuses., • Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position We are seeking a highly motivated and skilled Data Engineer to join our Research Informatics team within R&D. The successful candidate will play a key role in supporting Translational Genetics, Computational Chemistry, and AI/ML-driven discovery with software, AI tools, data requests, and building data infrastructure and pipelines that support immediate and longer term needs. This role will actively support Arrowhead's AI-enabled discovery initiatives by enabling high-quality, well-governed datasets for machine learning and advanced analytics. Responsibilities include preparing data for AI/ML workflows, supporting model training environments, and evaluating AI-powered tools (including LLM-based systems) to accelerate research insights, automation, and decision-making across R&D. The successful candidate will understand data and software needs for R&D teams, identify and access process gaps and opportunities to speed up research and optimize research results. This role also contributes to evaluating and deploying AI-enabled tools that enhance scientific productivity and insight. The best candidate will also design and implement robust data pipelines and architectures that integrate experimental and computational data across the research organization. A strong background in scientific informatics platforms (e.g., LIMS/ELN such as Benchling) and a passion for FAIR data principles are essential. Responsibilities • Support R&D teams with their day-to-day software, AI tools and data integration needs., • Evaluate, prototype, and adopt emerging technologies that advance data engineering, scientific AI, and research informatics capabilities., • Partner closely with Discovery Chemistry and Biology teams to ensure seamless data flow between experimental, analytical, and predictive workflows., • Develop and standardize data models and architectures to support research data management, metadata, and governance., • Build and manage integrations across scientific informatics platforms, including ELN, CDS, and analytical systems, to unify experimental and computational datasets., • Design, develop, and maintain scalable, reliable data pipelines to support R&D data integration, processing, visualization, and advanced analytics., • Influence architectural decisions that optimize data accessibility for AI development, analytics, and visualization tools., • Bachelor's or Master's degree in Computer Science, Data Engineering, Bioinformatics, or a related field., • 4+ years of professional experience in data engineering or data science, preferably within biotech, pharmaceutical, or scientific research environments., • Familiarity with data modeling, metadata management, data lineage, and data governance best practices., • Strong proficiency in Python, SQL, Git, and modern data engineering practices., • Experience with AI/ML frameworks and tooling (e.g., PyTorch, LangChain, or custom ML/AI pipelines)., • Experience supporting AI/ML workflows, including data preparation, curation pipelines, and model training environments., • Understanding of scientific data domains such as omics, assays, screening, or chemical data. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job Description We have an immediate need for a Paleontologist. This is an On-call position working on projects throughout California. This individual will be responsible for conducting paleontological monitoring of construction projects to include data collecting, interpretation of stratigraphic units, and salvaging of fossils. Qualifications • BS or BA degree in Geology or Paleontology and one year experience monitoring in the state or geologic province of the specific project AS or AA in Geology, Paleontology, or Biology and demonstrated two years’ experience collecting and salvaging fossil materials in the state or geologic province of the specific project., • Ability to identify vertebrate, invertebrate, plant, and trace fossils to class or lower taxonomic level in the field is desirable, • Ability to travel Upon a conditional job offer, a drug test and background check will be required. Compensation based on experience. (Paleontologist, Geology, Monitoring, Fossils, Geologic Province, Plants, Biology) Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website .

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, • 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 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 Powered by JazzHR DgRdMIsBZh

Job DescriptionCapricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most. We are seeking a Quality Assurance Associate I/II to join our team. This role is critical in scaling clinical production activities, ensuring compliance with cGMP and regulatory standards. The position will assist in batch record review, deviation investigations, label issuance, and management of controlled documentation across GLP/GCP/GMP systems. The ideal candidate is detail-oriented, organized, and passionate about driving quality excellence in a fast-paced environment.Responsibilities • Assist in batch record review and disposition for clinical product manufacturing, including label issuance, product packaging, and shipping activities., • Support the issuance, tracking, and archiving of controlled documentation in compliance with GxP (GLP/GCP/GMP) regulations., • Maintain and manage controlled records, including batch/test records, logs, reports, and quality management documentation., • Assist in preparing materials for internal audits and ensuring documentation readiness for regulatory inspections., • Help process and track training records to ensure company-wide GxP compliance., • Participate in the review and release of incoming materials in accordance with company standards., • Support controlled label issuance, including inventory tracking and updating lot numbers., • Collaborate with senior team members to improve and implement quality management systems and training programs., • Assist in preparing reports and documentation related to deviations, corrective actions, and change controls., • Support the maintenance and management of documentation systems, both manual and electronic, ensuring timely and accurate record-keeping., • Perform additional quality assurance tasks as assigned. Requirements, • Bachelor’s degree in a relevant field (e.g., Biology, Biotechnology, or related discipline) or equivalent experience., • 0-3 years of experience in a regulated environment (e.g., cGMP, GLP, GCP)., • Familiarity with regulatory standards such as 21 CFR 210 and 211, ICH, ISO9001, and FDA guidelines preferred., • Strong attention to detail and excellent organizational skills for managing documentation and records., • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and familiarity with database systems., • Strong written and verbal communication skills for effective collaboration and reporting., • Ability to work independently and as part of a team in a dynamic, fast-paced environment., • Comfortable gowning and working in classified areas as required. Work Environment / Physical Demands, • Primarily office-based with occasional time in GMP cleanroom environments for documentation and oversight tasks., • Requires prolonged periods of computer use for documentation and record management, and gowning for cleanroom work., • May involve lifting materials or equipment up to 20 pounds. Notice to Recruiting Agencies Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The Summer Intern, Biochemistry (Cell-Based Assay Development) will support discovery research at Arrowhead Pharmaceuticals by contributing to the development and execution of cell-based assays used for antibody screening. This internship offers hands-on laboratory experience supporting routine experiments, data analysis, and documentation that help accelerate research progress. The intern will work closely with scientists to generate high-quality data and gain exposure to assay development workflows within a collaborative research environment. This is an 11-week Summer Internship Program paying $24.00 per hour and requires full-time, onsite work five days per week at the designated location. Responsibilities • Maintain primary and established cell lines to support ongoing research activities., • Perform molecular biology tasks, including plasmid preparation and construction., • Generate experimental data using techniques such as multicolor flow cytometry and ELISA., • Isolate proteins, DNA, and RNA from cell cultures and conduct analyses using qPCR, SDS-PAGE, and Western blot., • Analyze, interpret, and organize experimental data with strong attention to detail., • Assist with routine instrument maintenance, inventory management, and general laboratory upkeeping., • Maintain accurate experimental records and contribute to reports or documentation as needed., • Bachelor's degree (completed or in progress) in Biological Sciences or a related field., • Completion of relevant coursework in biology or life sciences., • Familiarity with routine molecular and cellular biology techniques., • Hands-on experience with ELISA and flow cytometry., • Familiarity with cell-based assay development or antibody screening., • Proficiency in Microsoft Office applications. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job Description Duties: • Collaborate with research, analytical development and process development teams to develop, qualify/validate AAV gene therapy cell-based biological potency assays, protein chemistry assays, and molecular biology assays for process monitoring and drug product release, specifically droplet digital PCR, HPLC, ELISA, culture of primary mammalian cells, and cell based potency assays., • Participate in developing timelines, protocols and reports for assay transfers, qualifications / validations., • Author and review QC analytical SOPs, protocols, and reports as needed, • Ensure the timely execution of all routine QC testing, data review, and preparation of summary reports, • Perform quality management activities such as deviation, CAPA, change control, investigation of OOS, OOT and anomalous results within the company QMS Qualifications: • BS or equivalent in relevant discipline with a minimum of 4 years of relevant industry experience or Master’s degree in relevant discipline with a minimum of 1 year of relevant industry experience, • Experience in pharmaceutical industry with a GMP testing focus, ideally covering the analytical method and testing lifecycle from development through commercial drug product testing, with experience in a GMP QC release testing role, • Experience with JMP statistical software a plus. Why Choose R&D Partners? As an employee, you have access to a comprehensive benefits package including: • Medical insurance – PPO, HMO & HSA, • Dental & Vision insurance, • 401k plan, • Employee Assistance Program, • Long-term disability, • Weekly payroll, • Expense reimbursement, • Online timecard approval Pay Scale: $112,000 - $117,000 (Dependent on Experience) R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. R&D Partners is an equal-opportunity employer. Company DescriptionR&D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire & outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL. The cornerstone of our success: a knowledgeable and experienced recruiting team. Our life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.R&D Partners is a national staffing firm focused in the areas of: Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined staffing experience providing consulting, direct hire & outsourcing solutions with our west coast offices in San Francisco, Redwood City and San Diego, CA and our east coast offices located in Harrisburg, PA and Tampa, FL.\r\n\r\nThe cornerstone of our success: a knowledgeable and experienced recruiting team.\r\n\r\nOur life sciences recruiters, clinical research recruiters and engineering recruiters are uniquely specialized. After a detailed assessment of our clients’ needs, we can then identify appropriate candidates utilizing our established network of professionals. R&D Partners takes a proactive approach to recruiting, establishing relationships with experienced passive candidates so when the time is right, we can combine our candidates’ talents with our clients’ opportunities.

Job DescriptionSummary: The Senior Research Associate, Protein Sciences will play a key role in advancing our mission to develop novel therapeutics for cardiometabolic diseases. This position will primarily support the expression and purification of therapeutic candidates and assist with molecular cloning efforts, as well as analyze and present data and contribute scientific insights to drive our research forward. The Senior Research Associate will collaborate closely with cross-functional teams to accelerate progress, delivering reproducible, reliable data and solutions that help move promising therapies closer to patients who need them most. • Manage the expression and purification of proteins in mammalian cell systems, supporting multiple teams and molecular biology efforts as needed., • Develop and employ processes to produce endotoxin-free material., • Operate and maintain relevant laboratory equipment including incubators, biosafety cabinets, FPLCs, and other related instruments., • Review and contribute to the creation and revision of SOPs related to expression and purification practices and maintain accurate reporting in an electronic lab notebook system., • Knowledge of mammalian cell transfection techniques, especially lipofection, for CHO and HEK293 cells., • Familiarity with chromatography techniques such as protein A, ion exchange, Ni-NTA, and desalting., • Knowledge of endotoxin-removal procedures and methods for maintaining instrumentation to prevent endotoxin contamination., • Experience with FPLC operation and troubleshooting, particularly using ÄKTA Avant or ÄKTA Pure systems.Experience with molecular biology techniques, including cloning (restriction enzyme digestion/ligation, Golden Gate assembly, or Gibson assembly), bacterial transformation and culture, and DNA preparation and characterization., • Strong analytical and problem-solving skills with attention to detail., • Excellent organizational and time-management abilities., • Strong verbal and written communication skills.Ability to work both independently and collaboratively in a fast-paced environment.

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The Pharmacovigilance Systems Intern will support discovery research at Arrowhead Pharmaceuticals by contributing to laboratory projects that strengthen experimental capabilities and support program progress. This internship offers hands-on experience working with biological assays, data analysis, and scientific collaboration in a research environment. The intern will work alongside experienced scientists and gain exposure to laboratory workflows that help advance understanding of RNA biology. This is an 11-week Summer Internship Program paying $26.00/hour and requires full-time, on-site work five days per week. Responsibilities • Develop an understanding of the scientific background and workflow for RNA isolation assays and related experimental approaches., • Under supervision, establish and optimize assay parameters and conditions for isolating RNA from specific cellular compartments., • Perform experimental readouts using multiple methods to confirm assay performance and results., • Analyze experimental data and organize results using appropriate analytical tools., • Maintain accurate and well-organized experimental records., • Communicate findings and present results to the project team during meetings., • Currently enrolled student in an accredited university Master's degree program in Biology or a related field., • Familiarity with RNA-related techniques., • Hands-on experience with biological laboratory techniques., • Strong verbal and written communication skills., • Excellent problem-solving and analytical skills., • Excellent verbal and written communication skills, including comfort presenting in group settings., • Strong problem-solving and organizational skills., • Previous experience with RNA isolation techniques., • Familiarity with Microsoft Excel and GraphPad Prism., • Strong interest in RNA biology, assay development, or discovery research. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

Job DescriptionSalary: $80K - $85K, depending upon experience Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to build lasting partnerships that enable the life sciences industry to accelerate discovery and innovation in research and manufacturing. We can offer you the chance to build on your skills and knowledge while working among experts in their fieldsand with cutting-edge instrumentation. Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment.We aim to recruit the best people who stand out among their peers and embody our Core Values: • Client Focused: We only succeed when our clients succeed., • Outstanding: We deliver meticulous results through outstanding performance., • Good: We act ethically and morally., • Employee-Centric: We honor and support our employees., • Nimble: We are prepared to adapt in an ever-changing industry., • Team-Oriented: We collaborate with each other and with our clients. We currently have a role available for an Experienced Pharma Biophysical Chemist. Job duties include, but are not limited to: • Execute protein purification and characterization using techniques such as SDS-PAGE, DSF, HPLC, FPLC, BLI, and other biophysical assays., • Prepare, analyze, and document samples with accuracy and efficiency, ensuring compliance with laboratory standards., • Maintain organized lab operations, including inventory management and meticulous record-keeping., • Analyzing data using Excel and/or custom analysis software., • Manage multiple projects concurrently, delivering high-quality results within established timelines., • Presenting project data at meetings as needed. Job requirements include, but are not limited to: • BS degree in Biology or relevant field with 5+ years of laboratory experience or MS degree with 2-5 years of laboratory experience (biotech or pharma experience preferred)., • Hands-on experience with protein purification and analytical techniques; familiarity with chromatography and biophysical instrumentation preferred., • Strong foundation in protein biophysics and structural biology, including protein folding, stability, and conformational dynamics; experience with structural techniques (e.g., cryo-EM, X-ray crystallography) and biophysical characterization methods is advantageous., • Excellent communication skills verbal and written., • Works well both as a team and as an individual., • Demonstration of excellent team player skills, very strong attention to detail, very strong problem-solving skills, a high level of learning agility, and the ability to work across functions. The ideal candidate will be enthusiastic and self-motivated, with the leadership and communication skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery. This job posting will close by 4/1/2026 or when a candidate is identified, whichever comes first.

Job DescriptionSalary: $60-$65K, depending upon experience Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to build lasting partnerships that enable the life sciences industry to accelerate discovery and innovation in research and manufacturing. We can offer you the chance to build on your skills and knowledge while working among experts in their fieldsand with cutting-edge instrumentation. Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment.We aim to recruit the best people who stand out among their peers and embody our Core Values: • Client Focused: We only succeed when our clients succeed., • Outstanding: We deliver meticulous results through outstanding performance., • Good: We act ethically and morally., • Employee-Centric: We honor and support our employees., • Nimble: We are prepared to adapt in an ever-changing industry., • Team-Oriented: We collaborate with each other and with our clients. We currently have a role available for a Pharma Biophysical Chemist. Job duties include, but are not limited to: • Execute protein purification and characterization using techniques such as SDS-PAGE, DSF, HPLC, FPLC, BLI, and other biophysical assays., • Prepare, analyze, and document samples with accuracy and efficiency, ensuring compliance with laboratory standards., • Maintain organized lab operations, including inventory management and meticulous record-keeping., • Analyzing data using Excel and/or custom analysis software., • Manage multiple projects concurrently, delivering high-quality results within established timelines., • Presenting project data at meetings as needed. Job requirements include, but are not limited to: • BS degree in Biology or relevant field with 2-4 years of laboratory experience or MS degree with 0-2 years of laboratory experience (biotech or pharma experience preferred)., • Hands-on experience with protein purification and analytical techniques; familiarity with chromatography and biophysical instrumentation preferred., • Strong foundation in protein biophysics and structural biology, including protein folding, stability, and conformational dynamics; experience with structural techniques (e.g., cryo-EM, X-ray crystallography) and biophysical characterization methods is advantageous., • Excellent communication skills verbal and written., • Works well both as a team and as an individual., • Demonstration of excellent team player skills, very strong attention to detail, very strong problem-solving skills, a high level of learning agility, and the ability to work across functions. The ideal candidate will be enthusiastic and self-motivated, with the leadership and communication skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery. This job posting will close by 4/1/2026 or when a candidate is identified, whichever comes first.

Job DescriptionSalary: $60K-&70K, DOE Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to build lasting partnerships that enable the life sciences industry to accelerate discovery and innovation in research and manufacturing. We can offer you the chance to build on your skills and knowledge while working among experts in their fields and with cutting-edge instrumentation. Cogent Scientific offers competitive pay (with relocation bonus as needed), attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment.We aim to recruit the best people who stand out among their peers and embody our Core Values: • Client Focused: We only succeed when our clients succeed., • Outstanding: We deliver meticulous results through outstanding performance., • Good: We act ethically and morally., • Employee-Centric: We honor and support our employees., • Nimble: We are prepared to adapt in an ever-changing industry., • Team-Oriented: We collaborate with each other and with our clients. We currently have a role available for a Pharma Cell Biologist to join our San Diego based team. Job duties include, but are not limited to, the following: Maintain and culture mammalian cells, including both adherent and suspension cell lines. Prepare, optimize, and maintain various cell culture media, supplements, and reagents. Perform routine cell passaging, counting, viability assessment, and cryopreservation. • Hands-on experience with mammalian cell culture, including adherent and suspension cells is a must. Job requirements include, but are not limited to: • BS/MS degree in Cell/Molecular Biology (or related field) and at least 1 year laboratory experience in industry is required., • Team player mentality with strong written and verbal communication skills. Will be required to work collaboratively with cross-functional teams including structural biology, molecular biology, biochemistry, and biophysics., • The ideal candidate will be organized, comfortable with multi-tasking, enthusiastic, self-motivated and details oriented, with the skills necessary to operate effectively in a fast-paced multidisciplinary environment with flexibility and an adaptable approach to goal delivery. This job posting will close by March 31st 2026 or when candidates are identified, whichever comes first.

Job DescriptionAbout GenScriptGenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.About ProBioProBio proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio's total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing. Job Scope: The Business Development Manager will drive revenue growth across GenScript's GMP Gene Editing and GMP Biologics Manufacturing portfolios. This individual will support sales of GMP-grade nucleic acid reagents (including guide RNAs, ssODNs, long ssDNA, dsDNA HDR templates, and custom endonucleases) as well as GMP peptide and recombinant protein manufacturing services supporting vaccines, protein therapeutics, and advanced cell and gene therapy programs. This role requires strong technical fluency in gene editing or biologics development, outstanding consultative selling skills, and the ability to collaborate cross-functionally to deliver world-class customer experience. This role will support the West Coast territory and can be based remotely in California, Arizona, Washington, Oregon or another nearby state. Key Responsibilities: Sales & Revenue Growth • Identify, prospect, and close new business for GMP gene-editing reagents and GMP peptide/protein manufacturing services., • Develop and execute a territory sales plan to meet or exceed monthly, quarterly, and annual revenue targets., • Manage the full sales lifecycle, including lead generation, discovery, scoping, proposal creation, negotiation, and closing., • Build strong relationships with customers in cell therapy, gene therapy, vaccine development, and biologics R&D., • Serve as a technical resource for GMP manufacturing capabilities spanning:, • sgRNA, pegRNA, and custom guide RNA, • ssODNs and long ssDNA, • Linear dsDNA HDR donors (covalently closed), • Custom endonucleases and engineered proteins, • GMP peptides and recombinant proteins, • Translate complex scientific concepts into clear value propositions for R&D, technical, and CMC stakeholders., • Partner with Marketing, Project Management, Manufacturing, Quality, and R&D to ensure seamless customer onboarding and project execution., • Communicate customer needs, trends, and feedback internally to refine service offerings and operational capabilities., • Attend conferences, trade shows, and on-site customer meetings (15–25% travel)., • Expand GenScript's presence through networking with KOLs, biotech leaders, and strategic partners. Education & Experience • Bachelor's degree in Biology, Biochemistry, Molecular Biology, Biotechnology, or related field required; Master's or MBA preferred., • 3+ years of business development or sales experience in CDMO/CRO services within gene editing, biologics manufacturing, or adjacent markets., • Demonstrated success in consultative technical selling and achieving revenue targets., • Strong understanding of CRISPR workflows, HDR template design, and/or biologics development., • Excellent relationship-building, communication, and negotiation skills., • Ability to independently manage a dynamic pipeline within a fast-paced environment., • Proficiency with Microsoft Office, Salesforce/Dynamics, and virtual communication platforms., • Highly motivated, organized, detail-oriented, and capable of leading scientific and commercial discussions. #LI-EB1 #GS GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law. GenScript USA Inc./ProBio Inc. maintains a drug-free workplace. Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.

Job DescriptionCapricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most. We are seeking an individual to join our Quality Compliance department. This role conducts internal and external audits to ensure our biopharma operations comply with applicable regulations, standards, and company procedures. The ideal candidate brings hands-on GMP/GxP auditing experience within the life sciences industry and partners cross-functionally to drive continuous improvement and a strong culture of compliance.Responsibilities • Internal Audits: Plan, conduct, and report risk-based GxP audits across manufacturing, QC, labs, validation, and supply chain., • Supplier Audits: Lead and support vendor audits and monitor ongoing supplier performance, as needed., • Audit Execution: Develop audit agendas, checklists, and sampling strategies aligned with regulatory expectations., • Reporting & CAPA: Issue clear audit reports, classify findings, and track CAPA effectiveness to closure., • Inspection Readiness: Support regulatory inspection readiness., • Gap Assessments: Assess compliance against regulations and industry standards and recommend improvements., • Cross-Functional Partnership: Collaborate with QA/QC, Manufacturing, Regulatory, Supply Chain, and IT to strengthen quality systems., • Metrics & Communication: Maintain audit schedules, dashboards, and communicate status and trends to management., • Quality Improvement: Support SOP development, training, and continuous improvement initiatives., • Additional Support: Willing to support activities related to post-marketing safety and surveillance and additional responsibilities as needed.Minimum Qualifications, • Education: Bachelor's degree in a scientific or technical field (e.g., Chemistry, Biology, Engineering) or equivalent experience., • Experience: 2–5 years of auditing experience within biopharma, biotech, medical devices, or related regulated industry, including audits against quality system elements (Deviation, CAPA, Change Control, Training, Document Control)., • Regulatory Knowledge: Working knowledge of FDA 21 CFR Parts 210/211, ICH Q-series, EU GMP, and GxP principles., • Communication: Strong writing skills and attention to detail; able to produce clear, evidence-based audit reports., • Technical Proficiency: Proficiency with risk-based auditing, root cause analysis, and CAPA effectiveness verification., • Stakeholder Management: Excellent communication and stakeholder management skills; comfortable engaging at all levels.Preferred Qualifications, • Certification: Certified Quality Auditor (CQA) – ASQ, or equivalent certification; candidates without certification must demonstrate the ability and willingness to obtain it within a defined timeframe., • Vendor Oversight: Experience auditing CMOs/CDMOs and complex supply chains., • Digital/Data: Background with data integrity, CSV, Annex 11, and Part 11 assessments., • Specialized Manufacturing: Exposure to biologics, cell & gene therapy, aseptic processing, or sterile manufacturing., • Post-Marketing: Knowledge of ISO 9001/13485 and quality systems related to post-marketing safety and surveillance (as applicable).Core Competencies, • Integrity & objectivity in evidence gathering and reporting., • Risk-based thinking and prioritization., • Analytical problem-solving and pragmatic recommendations., • Collaboration across functions and suppliers., • Time management, organization, and follow-through.Work Conditions, • On site based in San Diego. Notice to Recruiting Agencies Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.

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, • 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 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 Powered by JazzHR 9oKusGlLSA

Job Description About The Bishop’s School Founded in 1909 and affiliated with the Episcopal Church, The Bishop’s School is an independent, all-gender college-preparatory day school servingin 800 students in grades six through twelve. The School is located on a historic campus in the heart of La Jolla, just 10 miles north of downtown San Diego. With a student-teacher ratio of approximately 9 to 1, Bishop’s is known for academic, artistic, and athletic excellence while celebrating character development, diversity, inclusion, and belonging. Last year’s applicant pool drew from 72 zip codes and 168 middle and high schools throughout San Diego County and beyond. Fifty-one percent of the student population self-identify as students of color. Additionally, over $4 million in need-based grants is awarded annually. What is Essential about Being a Teacher at Our School? The Bishop’s School seeks engaging, collaborative, dynamic, and learner-centered teachers. We seek candidates who hold high expectations for students, design learning experiences that prioritize adolescent well-being and belonging, are enthusiastic about working on teams and are eager to pursue growth in their teaching practice. Our goals are to foster curiosity, encourage active student engagement, encourage collaboration in the classroom and direct students to take ownership of their learning. Position Summary Description The Bishop’s School seeks a full-time Chemistry Teacher beginning August 2026. The ideal candidate will have a background in teaching chemistry at the high school level, and will demonstrate interdisciplinary capacity with the ability to teach additional subjects within the department such as biology, environmental science, or biochemistry. The Science Department seeks candidates who are enthusiastic about working with teaching teams and other departmental colleagues to develop, iterate upon, and align lab-focused, inquiry-based, student-centered curricula throughout the Science Department. Bishop’s faculty communicate regularly with students, parents and administrators on student progress and are regularly expected to supervise students in out-of-classroom activities during the school day and after school. In addition to teaching, faculty serve as advisors to students and offer daily office hours. Responsibilities Include: • Teach three sections of chemistry (with a lab component), and a semester-length elective course, • Meaningfully engage with students through advisory, • Engage in co-curricular activities as assigned, • Employ a variety of pedagogical approaches to teach students with an array of learning styles, • Be available to students during office hours and at other times throughout the day to provide guidance and support as needed, • Collaborate with departmental colleagues in the development of curriculum and meaningful, relevant, learner-centered classroom experiences, • Provide timely communication to students and their parents/guardians relating to grading and current academic standing, • Uphold the School’s Core Values, • Demonstrate professionalism and tact, • Stay up to date on industry standards, trends, developments and legal updates, • Make timely and ethical decisions both systematically and under pressure, • Comply with School’s reporting policies and procedures, • A bachelor’s degree (B.S.) in chemistry or a related field; advanced degree in chemistry or education (preferred), • A minimum of 3 years of teaching experience in high school chemistry, • Experience teaching at the honors or AP level, • Excellent chemistry content knowledge, • Ability to teach biology in addition to chemistry (preferred), • Knowledge of laboratory safety standards and best practices, • Interest in supporting current co-curricular programs, • An unequivocal passion for working with adolescents and supporting them in all facets of their lives, • Ability to integrate technology into instruction, • Eagerness to collaborate with other department members in creating meaningful, relevant, learner-centered classroom experiences, • Ability to communicate effectively in writing and verbally with students, parents, faculty, staff, administrators, and the broader school community, • Strong work ethic, time management, verbal, written language, and interpersonal skills, • Irrespective of own religious orientation, ability to support the School’s mission and values as a school founded in the Episcopal tradition In addition to competitive salary, The Bishop's School offers a comprehensive menu of benefits including medical, dental, and vision insurance plans, generous PTO, robust professional development opportunities, and chef-prepared lunch provided to employees at no charge on a daily basis when school is in session. Application Deadline Interested candidates are encouraged to use the link provided to submit a resume, cover letter, and a sample of work (a lesson plan, lab, or project) to the attention of Ian Hayden, Dean of Faculty. Applications received by January 20, 2026 will be afforded priority consideration. Applications will be reviewed on an ongoing basis until the position is filled. Please do not contact the school directly. EEO The Bishop's School is an equal opportunity employer. We are a diverse community of professionals that broadly reflects the people of the San Diego area and the United States at large. We aim to align our hiring process with our mission and institutional goals. All qualified applicants will receive consideration for employment and will not be discriminated against on the basis of race, color, religion or religious practices, sex, gender identity or expression, sexual orientation, citizenship status, national origin, age, ability status, military status, unemployment status or any other category protected by applicable local, state, or federal laws. The Bishop's School takes affirmative action in support of its policy to employ and advance all qualified candidates. Powered by JazzHR cATjPWRcJB

Job DescriptionSalary: $150,000 - $200,000/year + bonus As a subject matter expert, this role will support the execution and delivery of clinical and translational biomarker services for Sponsor and internal R&D studies. This role will function to lead and support immunostaining assay development, biomarker projects, and advanced image analysis including developing and applying AI-driven image analysis algorithms to quantitatively assess histopathology and biomarker data, while also serving as a scientific partner to clients from study design through data interpretation and presentation. The role will work cross-functionally with pathologists, laboratory technicians, scientists, project operations and business development teams, and will directly support pharmaceutical and biotechnology clients in planning, executing, and interpreting biomarker studies across preclinical and clinical programs. What you'll be doing: Lead/Support Scientific Efforts for Computational and Digital Pathology • Act as a scientific interface with clients, participating in client meetings, protocol reviews and data review meetings, • Provide expert input on design and conduct of clinical or translational studies incorporating biomarker endpoints and omics and non-omics techniques including but not limited to immunostaining, proteomics, spatial biology, computational and digital pathology., • Prepare and/or support the preparation and review of project plans, analysis plans and study reports, abstracts, manuscripts, and technical reports., • Perform and/or support the analysis and interpretation of biomarker data including providing clear, scientifically rigorous data visualizations, analyses, and summaries. Assay Development, Image Analysis, and Algorithm Development • Partner with laboratory technicians to support immunostaining assay development, optimization, and validation., • Define analytical endpoints, scoring strategies, and quality control metrics aligned with assay performance., • Contribute to assay validation documentation and analytical reports as required., • Develop, validate, and maintain image analysis pipelines for immunostaining (IHC), immunofluorescence (IF), in situ hybridization (ISH), and multiplex assays., • Design and implement AI/machine learning algorithms for tissue segmentation, cell characterization, and biomarker quantification., • Collaborate with pathologists through end-to-end workflows including assay development, validation, quantitative read-outs and interpretation., • Ensure traceability, reproducibility, and documentation of analysis workflows. Business Development Support • Assist with business development activities including participating in client meetings, requests for proposal (RFP) responses, project pricing, protocol review, and bid defenses as needed., • Provide advice to sponsors seeking guidance, • Assist in the development of sales, marketing and promotional materials as needed. Product and Service Innovation Support • Contribute to continuous improvement of computational, digital pathology, spatial biology and translational research capabilities., • Assist in the development of our product/service platforms to ensure all stakeholder requirements are being considered, documented, and translated to the final solution., • Participate in brainstorming meetings and functionality reviews. Qualifications • Post-graduate degree / professional designation; 7-9 years related experience, plus continuous training and knowledge/skills upgrading, • Strong experience with digital pathology and image analysis, • Solid understanding of histopathology and immunostaining techniques, • Experience working in CRO, laboratory, biopharma and/or regulated research environment, ideally supporting clinical and translational research studies, • Experience presenting data to external stakeholders or at scientific meetings, • Scientific rigor and attention to detail - able to communicate complex scientific concepts and results clearly to all stakeholders, • Strong written and oral English communication skills, problem-solving and analytical thinking, • Ability to manage multiple projects in fast-paced environment with a collaborative mindset across disciplines Note: Compensation is dependent on the unique experience, skills, and education the successful candidate brings to the role. The range above represents an estimated base salary that we would expect to compensate at, but we encourage applicants to speak with the member of the TA team if contacted for an initial phone screen should your expectations differ from those listed above.

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. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Eurofins BioPharma Product Testing is seeking a Microbiology Lab Technician to support routine microbiological testing at our San Diego site. This position is a professional laboratory role suited for early-career microbiology professionals with a Bachelor’s degree in Microbiology or a related life science who are looking to develop their skills in a regulated laboratory environment. This role supports pharmaceutical and medical device microbiology testing performed under GMP and ISO-classified cleanroom conditions. The successful candidate will perform routine testing, documentation, and laboratory support activities in accordance with established procedures, while building technical proficiency and regulatory knowledge through hands-on experience and structured training. The ideal candidate will have relevant laboratory experience, typically gained through academic coursework, internships, or early-career industry roles, and a strong foundation in microbiological techniques. This position offers an opportunity to gain experience with compendial methods, environmental monitoring, and regulated laboratory operations, with opportunities for growth as independence, technical capability, and confidence increase. · Perform routine microbiological testing in accordance with approved SOPs, including but not limited to: o Microbial Limits testing (USP <61> / <62>) o Sterility testing (USP <71>) o Endotoxin testing (USP <85>) · Prepare, label, and verify microbiological culture media and reagents · Conduct basic microbiological techniques such as plating, colony enumeration, and Gram staining · Support Environmental Monitoring (EM) activities in ISO-classified cleanrooms, including surface, air, and personnel monitoring · Accurately document laboratory activities in compliance with GMP, GLP, and data integrity requirements · Enter test results into LIMS and support data review under supervision · Operate and maintain laboratory equipment (e.g., incubators, biosafety cabinets, autoclaves) following training and established procedures · Maintain a clean, organized, and inspection-ready laboratory workspace What We Offer · Hands-on training in regulated pharmaceutical and medical device microbiology · Exposure to a broad range of microbiological test methods and client applications · Technical skill development and clear opportunities for career growth · Competitive compensation and comprehensive benefits package · Collaborative, science-driven team environment · Follow laboratory safety, gowning, aseptic technique, and contamination control practices · Support investigations, deviations, and corrective actions as assigned · Participate in training and continuous improvement initiatives Qualifications Required Qualifications · Bachelor’s degree in Microbiology, Biology, or a closely related life science · Relevant laboratory experience gained through academic, internship, or early career industry roles-career industry roles · Working knowledge of basic microbiological techniques and aseptic practices · Strong attention to detail and ability to follow written procedures · Ability to work effectively in a regulated laboratory environment · Basic computer proficiency (Microsoft Office and electronic data systems) Preferred Qualifications · Experience in a GMP, GLP, or ISO-regulated laboratory environment-regulated laboratory environment · Familiarity with pharmaceutical or medical device microbiology · Exposure to USP or other compendial test methods · Experience with Environmental Monitoring or cleanroom operations · Experience using a Laboratory Information Management System (LIMS) Physical & Work Environment Requirements · Ability to work in ISO-classified cleanroom environments with gowning requirements · Ability to stand for extended periods and perform repetitive laboratory tasks · Ability to lift and move laboratory materials and equipment as required · Flexibility to work assigned shifts and occasional overtime based on business needs Additional Information Position is full-time, first shift, Monday - Friday, 8:00pm - 5:00PM. Candidates currently living within a commutable distance of San Diego, CA are encouraged to apply. The pay range of this role is $24/h - $28/h depending on related experience. • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match

Job DescriptionDescription: An excellent opportunity exists to work for a government contractor with competitive compensation and work-life balance. Posterity Group is seeking experienced Dental Assistant at the Naval Medical Center San Diego. • Certificate or associate degree as a dental assistant/technician from a program accredited by the Commission on Dental Accreditation (CODA) of the American Dental Association (ADA) and 12 months experience within the preceding 36 months., • Certification from a military dental technician or dental assistant school and 12 months experience within the preceding 36 months., • Certification from a Red Cross Dental Assistant course and 12 months experience within the preceding 36 months., • 36 months experience within the preceding 60 months as a dental assistant in a private practice or a military clinic., • Membership in good standing with the American Association of Dental Assistants with required continuing education and 12 months experience within the preceding 36 months., • Graduation from a state accredited program for dental assistants or dental technology within the preceding 12 months., • All training must have included a course in radiation physics; radiation biology; radiation health, safety, and protection; X-ray films and radiographic film quality; radiographic techniques; darkroom and processing techniques; film mounting; and digital radiographic processing techniques. Requirements:, • Performs duties in providing assistance in one or more phases of complex/difficult restorative, prosthodontic, oral surgical, endodontic, or periodontal treatment. Receives and schedules patients for treatment., • Obtains and records related medical history of patient. Charts examination and treatment information. Records information on prescriptions., • Sterilizes instruments, materials, and equipment; prepares surgical trays. Maintains dental equipment in a clean and operative condition., • Assists dentist at chair side. Performs intra-oral procedures as directed by dentist. Takes preliminary impressions for study models, removes sutures, places and removes rubber dams, perio-packs, matrix bands, and wedges., • Relays dentist’s instructions to patient for post-treatment care. Instructs patient in proper dental techniques, care of appliances, and causes of dental decay., • Operates dental X-ray equipment to take intra and extra oral radiographs. Maintains, cleans, and performs minor repairs on X-ray equipment and materials., • Pours and trims models from impressions and constructs custom impression trays. Maintains a variety of recurring reports related to dental activities.

Job DescriptionSalary: 78k-83k JOB SUMMARY This position works directly with the Quality Systems Manager and Quality Assurance Associates toward the implementation of a Quality Management System in compliance with ISO 13485. The Quality Assurance Lead will provide support in the implementation, maintenance, and improvement of company-wide Quality Management System procedures, and support processes. Proactively monitors the various elements of the QMS to help ensure compliance with quality system regulations and applicable national and international standards. RESPONSIBILITIES * Provide support to internal functions in the application, maintenance, and improvement of quality systems, procedures, and department-specific processes. * Support the trending of quality systems such as deviation, change control, CAPA, complaints for management review processes. * Lead or support quality functions such as supplier qualification and surveillance program. * Lead or support internal audit programs including planning, implementation, report generation, corrective action issuance to closure. * Writes new standard operating procedures or revises existing documentation utilizing document control systems. * Creates and/or revises Quality Assurance documents such as gap analysis, risk assessment, reports to support compliance with regulatory requirements. * Performs review of completed records from materials management, manufacturing, quality control, tech transfer etc. * Provide support during regulatory inspections. * Conduct local and global training on key elements of the QMS, including CAPA, Complaint, and Internal Audit. * Execute projects and complete other duties as assigned. QUALIFICATIONS * Bachelors degree in biology, Engineering, or science-related field. * 4+ years of Quality Assurance experience in the Biotech industry. Knowledge of ISO 13485, 14971 is preferred. * 3+ years of experience in GMP environments including knowledge of change management principles and industry standard QMS applications. * Strong interpersonal teamwork and organizational as well as effective oral and written communication skills. * May require domestic and international travel (5-10%)

Job Description Job Description: We are looking for a highly talented Quality Assurance Supervisor to join our team. Responsible for supporting and overseeing production and manufacturing quality. Furthermore, you are responsible for exercising your authority to stop manufacturing if, and when product is out of specification, and to report any, and all product quality issues. This position may require travel to Pomona. Duties / Responsibilities: • Ensure incoming materials, in process and all finished products meet specified requirements., • Must be able to work in coordination with production line workers., • Ensure that customer complaints are investigated and resolved with the necessary corrective and preventive actions., • Develop and validate methods for analyzing and products to ensure they meet specifications., • Develop quality metrics and assess trends for product or process implications., • Investigate product, and process deviations, identify root cause, and develop corrective and preventative actions., • Ensure quality in the initial start-up of new or modified product manufacturing., • Keep in constant communication with manufacturing plant supervisors to ensure guidelines are followed at bottling lines., • Serve as Quality Management Representative for the company with respect to government agencies compliance and regulations., • Formulate and recommend quality policy and strategy to executive management., • Monitor and review quality performance against company’s set objectives and take necessary action to advise process owners to strive for improvements., • Promote quality achievement and performance improvement throughout the organization., • Establish clearly defined quality standards and methods for manufacturing plant to follow., • Conduct various analytical testing of in-process materials, raw materials, to ensure quality control of products at the point of production, shipping, and arrival upon the job site, as per manufacturing quality control guidelines., • Analysis and evaluation of material and products at all stages of development process under stringent quality and time requirements., • Involve in procedure review and propose modifications and updates., • Anticipating additional resources, consumable, and equipment requirements as needed to ensure that work can be completed within the budgeted time., • Maintenance of a safe and orderly laboratory and insurance of compliance with all safety policies and practices., • Ensure housekeeping standards are maintained in and around the lab. Troubleshoot problems and review basic product specifications. Inspect, calibrate, and maintain testing equipment periodically. This job supervises the Quality Assurance Inspector. Requirements: • BS or BA, degree in Chemistry, Math, Applied Chemistry, Biology or related field preferred or equivalent combination of education and experience., • Experience supervising Quality personnel., • 3 to 5 years of experience in manufacturing and quality assurance in an ISO9001:2015 and/or AS9100D environment., • Knowledge and experience of statistical processes related to manufacturing., • Proficient in Microsoft office (excel, word, PowerPoint)., • Excellent communication, interpersonal skills, attention to details, organizational skills, analytical skills, investigative abilities to oversee and lead the quality control processes and procedures., • Ability to lift 10-25 lb. objects.

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., • 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., • 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 DescriptionBenefits: • Employee discounts, • Free uniforms, • Opportunity for advancement, • Paid time off, • Training & development "If you have enthusiasm, a positive attitude and good communication, we have a fun and fulfilling Personal Training Position just for YOU!" We understand that everyone knows they should exercise, and everyone wants to be fit and healthy. But, that is easier said than done given busy schedules, and in some cases somewhat beat-up bodies. Thousands of people every day enjoy the best possible workout for them at our 180 nationwide studios. The Exercise Coach brand was built upon the belief that staying strong and healthy shouldnt feel like a hassle! Our protocols combine our very own proprietary strength and interval high-tech technology with a 100% coach-guided process, which for the first time allows to actually measure an individuals muscular and metabolic makeup and then prescribe exercise that is perfectly appropriate for them. Our technology can adapt to the user, every second of every workout. Additionally, our clients receive instantaneous feedback throughout their workouts that helps them focus their efforts, which leads to increased results. And all of this is delivered in a safe, clean studio environment that is nothing like a regular gym filled with mirrors, clanging dumbbells, and loud music. Our studio is located in Rancho Bernardo and offers a casual, fun environment, top-of-the-line proprietary training equipment, and the opportunity to learn the inner-workings of a successful personal training studio. We want someone who enjoys working with people and making a difference in the lives of others... because that is what we do. Members of our team enjoy benefits like: • Access to state-of-the-art fitness technology, • Complimentary Membership - Be paid to improve your own strength and health!, • Company-paid certifications, • Paid for all scheduled hours (not just for training), • Opportunity for career advancement, • Conducting initial consultations, • Lead individual and small-group exercise sessions, • Track fitness results for clients and lead client education, • Measure success by tracking studio metrics, • Administration of client accounts, including the completion of all necessary forms, credit card charges, and data entry, • Contribute to and oversee the maintenance of a clean and well-organized studioNo fitness experience is necessary, but candidates with experience in personal training or small-group fitness instruction will receive priority consideration. All employees will receive full training in The Exercise Coach methods and technologies and must be able and willing to participate both in our exercise and nutrition methodology. If you would like to inspire and empower people to enjoy the strength, wed love for you to consider joining our team! Certification: • Successful completion of:, • The Exercise Coach Certification Course, • Nutrition Playbook Certification Course, • Valid CPR/AED certificate from a nationally-recognized provider., • Passion for Health & Fitness: This is where it all begins!, • Good Communication Skills: You must be comfortable conversing in person and on the phone and know how to conduct yourself professionally, and deliver clear instructions to the clients., • People skills and personality: You must LOVE working with people! As mentioned above you must be very comfortable working with people. This is an exciting studio and you must be able to show your clients energy and excitement while working with them., • Health and Fitness Education: A college degree in a health-related field is nice, but not required. However, fundamental knowledge of exercise science and human biology is essential. You do not need a great deal of personal training experience, but you should have a working knowledge of the human body and the various components of good health and fitness.Preferred Skills:, • Basic nutrition knowledge, • College degree in a health-related field, • Experience with various strength training applications, • Experience working with older adults and various limitations

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., • 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., • 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 Invivoscribe is an industry pioneer, dedicated to Improving Lives with Precision Diagnostics®. Invivoscribe has been the global leader in driving international standardization of testing and accelerating patient access to the newest and best cancer treatments for over 30 years. Headquartered in sunny San Diego, California with locations across the world, we offer a comprehensive portfolio of products and services. We work with key collaborators to develop molecular assays, reagents, controls and bioinformatics tools under ISO 13485 design control that are used by over 700 clinical laboratories in over 160 countries. Our global network of laboratories offers internationally standardized next generation molecular and flow cytometry panels to support drug development and accelerate drug approvals worldwide. We work with pharmaceutical partners and international regulatory agencies across the globe to develop companion diagnostics, which are necessary to gain approval of new drugs and treatments for cancer patients. Our harmonized ISO15189 accredited and CLIA/CAP clinical laboratories offer a test menu focused on biomarkers which are clinically actionable to support therapeutic decisions, measurable residual disease (MRD) testing, patient stratification, and trial enrollment, all designed to accelerate approvals of new oncology drugs and treatments. For 30 years, we have been at forefront of precision diagnostics, and we’re just getting started! We are looking to add a Senior Bioinformatics Scientist. The Senior Bioinformatics Scientist is a hands-on technical leader with advanced knowledge of scientific principles and concepts who designs, builds, and validates production-grade bioinformatics software and scalable NGS pipelines (on-prem and cloud) to diagnose and track disease (MRD) for clinical and research applications. This role independently identifies opportunities, defines technical roadmaps, and leads delivery from requirements and design through implementation, verification/validation, release, and lifecycle support. Core Responsibilities Include: • Lead the design and development of bioinformatics software and pipelines to support Whole Genome Sequencing (WGS), hybrid-capture, and amplicon based NGS assays., • Work in close collaboration with the R&D and clinical lab teams, representing bioinformatics from a technical leadership role., • Evaluate and develop novel methods and external tools; perform benchmarking and method comparisons, and document recommendations and decisions; own projects end-to-end., • Develop reproducible, testable bioinformatics software using modern engineering practices (git, code review, unit/integration tests, CI/CD, containerization), and workflow technologies (e.g., Nextflow)., • Apply deep Next Generation Sequencing (NGS) analytics expertise and partner with scientific stakeholders to translate bioinformatics outputs into actionable conclusions., • Lead bioinformatics software development for CAP/CLIA/NYA environments, including requirements definition, design documentation, verification and validation planning/execution, traceability, change control, and release documentation., • Ph.D. degree in bioinformatics, computational biology, molecular biology, or related field with, typically, 8+ years applicable post-graduate experience. M.S. degree in bioinformatics or related field and 10+ years of applicable post-graduate experience. Equivalent combination of education and experience may be considered., • Advanced proficiency with Linux and strong programming skills (Python, bash required; additional languages welcome)., • Experience building and/or leveraging AI agents and LLMs for various tasks and optimization of software development., • Demonstrated experience designing and building production bioinformatics pipelines for WGS/WTS assays., • Hands-on experience developing and operating bioinformatics software in the cloud, including workflow execution at scale and management of compute/storage costs., • Experience collaborating across multi-disciplinary teams and providing technical leadership through influence (with or without direct reports)., • Strong foundation in statistics and quantitative analysis of biological datasets., • Extensive background in immunology or cancer research is highly preferred., • Experience developing software in a regulated environment is a plus (e.g. IVD, IVDR, CAP/CLIA/NYS)., • A beautiful modern facility centrally located in San Diego County, with many jobs conducive to flexible scheduling and telework options., • A welcoming breakroom for gathering with hosted hot/cold beverages and healthy convenience foods, and an available micro-market to get you through the day., • A positive workplace culture with an emphasis on support, respect and belonging., • A diverse and inclusive work environment where you will learn, grow, and make new friends.

Job Description Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gene, thereby affecting the production of a specific protein. Arrowhead's RNAi-based therapeutics leverage this natural pathway of gene silencing. Arrowhead is focused on developing innovative drugs for diseases with a genetic basis, typically characterized by the overproduction of one or more proteins that are involved with disease. The depth and versatility of our RNAi technologies enables us to potentially address conditions in virtually any therapeutic area and pursue disease targets that are not otherwise addressable by small molecules and biologics. Arrowhead is leading the field in bringing the promise of RNAi to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and lung with a promising pipeline of preclinical candidates. Arrowhead's corporate headquarters is in Pasadena, CA with research and development teams in Madison, WI & San Diego, CA, and a state of the art manufacturing facility in Verona, WI. Our employees are nimble, science-driven innovators who are collaborating to bring new therapies to patients in need. The Position The AI & Computational Chemistry Intern will support discovery research at Arrowhead Pharmaceuticals by contributing to an AI-driven virtual compound library initiative. This internship offers hands-on experience working at the intersection of computational chemistry, cheminformatics, and machine learning to support early-stage drug discovery. The intern will play a meaningful role by executing focused technical tasks, improving computational workflows, and supporting model development, helping accelerate project timelines and enhance data quality across the discovery organization. This is an 11-week Summer Internship Program paying $24.00 per hour and requires full-time, onsite work five days per week at the designated location. Responsibilities • Curate, clean, and preprocess molecular and structural datasets to support AI model development and evaluation., • Contribute to algorithm prototyping, benchmarking, and computational experiments related to virtual compound library generation., • Help automate repetitive computational tasks using Python or related scripting tools to improve workflow efficiency., • Assist in development and evaluation of machine learning or deep learning models supporting virtual compound libraries., • Collaborate with scientists and engineers to test new ideas, troubleshoot issues, and iterate on computational designs., • Currently pursuing a Bachelor's degree in Computational Chemistry, Chemistry, Bioinformatics, Computer Science, Data Science, or a related technical field., • Basic proficiency in Python and familiarity with scientific or data-processing libraries (e.g., NumPy, pandas, RDKit, PyTorch, TensorFlow)., • Fundamental understanding of molecular structures, chemical representations, or machine learning concepts., • Strong problem-solving skills and ability to work independently within established computational workflows., • Hands-on experience with Linux environments, shell scripting, or GPU computing., • Prior research or project experience in AI, drug discovery, computational modeling, or molecular biology., • Familiarity with deep learning frameworks or cheminformatics toolkits., • Strong curiosity and motivation to learn at the interface of AI, chemistry, and biology. All applicants must have authorization to work in the US for a company. California Applicant Privacy Policy

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. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Leadership & Strategic Management • Team Oversight: Directly manage non-leadership employees and group leaders; handle scheduling, training, and fostering teamwork/morale., • Operational Excellence: Ensure laboratory operations meet the highest quality, efficiency, and safety standards (including Health, Safety & Environmental responsibilities)., • Strategic Planning: Identify departmental unmet needs, focus on team time management, and implement LEAN projects or new technologies., • Method Development: Lead the development, qualification, and validation of cell-based analytical test methods for drug products and drug substances. Design studies to elucidate the cellular mode of action (MoA) of drugs and characterize drug-target interactions and signaling pathways, • Assay Execution: Perform tissue culture-based potency assays, ELISAs, and molecular biology techniques (qPCR, ddPCR, flow cytometry, DNA/RNA extraction/purification)., • Laboratory Support: Maintain multiple cell lines, prepare solutions/culture media, and utilize automation and advanced pipetting techniques., • Regulatory Oversight: Ensure strict adherence to GXP (GMP/GLP) compliance; interface with the FDA and other regulatory agencies as needed. Track record of developing and validating GMP methods to support drug commercialization., • Scientific Review: Serve as the final reviewer for scientific rigor, conclusions, and the quality of reports sent to customers., • Technical Writing: Author SOPs, policies, and procedures; maintain accurate records and ensure the integrity of all laboratory work., • Accountability: Take ownership of reporting errors, deviations, or Out of Specification (OOS) occurrences promptly.Qualifications Degree: Bachelor’s, Master’s, or Doctorate in Biology, Chemistry, Biochemistry, or a related physical sciences Experience Levels: • Ph.D. with 10+ years of related experience., • Master’s with 15+ years of related experience., • Bachelor’s with 20+ years of related experience., • Communication: Exceptional oral and written communication skills for technical writing, client interaction, and professional peer engagement., • Computer Literacy: Advanced proficiency in Excel (formulas and linking spreadsheets) and general scientific software., • Professionalism: High attention to detail, self-motivated, adaptable, and willing to work overtime when necessary to meet group deadlines. Additional Information Position is full-time, first shift Monday - Friday 9:00am - 5:00pm. Candidates currently living within a commutable distance of San Diego, CA are encouraged to apply. The pay range of this role is $150,000 - $180,000 at a Associate Director or Director level depending on related experience. • Excellent full time benefits including comprehensive medical coverage, dental, and vision options, • Life and disability insurance, • 401(k) with company match

Job Description Who we are: Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies. At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market. Your next role as a Miracle Maker Maravai LifeSciences is seeking a #MiracleMaker to join our CDMO Commerical team as a Director, Commerical CDMO. As a Director, Commerical CDMO, you will oversee and develop CDMO Services sales and PgM teams. Position is reporting to the VP and GM of Trilink CDMO and this leader will have responsibility for CDMO sales strategies, mRNA service markets and strategic positioning, pricing, customer / program management and forecasting for the TriLink CDMO services business. This leader will evaluate market performance while developing corporate long-range plans, goals, and objectives to strategically increase revenue and CDMO capabilities. This leader will interact with varying levels of internal and external customers as well as our business partners internal to Trilink Global products and services with a team-focused approach for continuous improvement and revenue growth. Strong sales strategies, business acumen, mRNA market awareness, customer focus and mRNA CDMO program experience are essential. How you will make an impact: • Drive sales and program management for CDMO services (Pre IND through to BLA and Commercialization) by identifying, developing, and closing opportunities across biotech, pharma, diagnostics, and life sciences accounts and managing milestones across execution to provide a best in Class Customer experience., • Develop and manage individual(s) as a part of the CDMO Leadership team to achieve defined sales and business objectives across the CDMO Service portfolio., • Build and sustain executive-level relationships with key decision-makers to catalyze the sales process., • Drive the development of new preclinical and clinical service accounts leveraging Trilink CDMO Capabilities including Process Development, Analytical Services and GMP to support the Customer journey from IND though to BLA and Commercialization., • Own Global CDMO strategies, pipeline management, and accurate forecasting through CRM (Salesforce)., • Partner cross-functionally with Maravai / Trilink Global Marketing, Commercial and Product Management to align on account strategies and educational campaigns raising awareness of TriLink's CDMO capabilities., • Develop and implement effective educational campaigns to support expansion of CDMO services awareness pre-GMP, preclinical to GMP and IND, and through Phase 2/3 to BLA and Commercialization, • Represent TriLink at key conferences, symposia, and industry events; stay current on mRNA clinical trends, • Leverage VOC to inform marketing tactics and product development strategy., • Lead management and accuracy of proposals, MSAs, SOWs, and other high-quality client-facing materials., • Meet or exceed revenue and pipeline growth targets., • Develops and maintains tools to effectively review, analyze and expand TriLink CDMO services sales achievements and program execution vs. strategic goals, • Develops and maintains forecasting, analysis and market share attainment for TriLink CDMO services with a deep understanding of market position, costs, pricing and supporting analytics., • Stays current with industry trends and market intelligence, specifically with respect to TriLink's current CDMO services and capabilities, to understand key competitive issues in relation to process, timing, costs, pricing and business strategy, • Responsible for program management and customer satisfaction as we manage contract milestones and Change Orders across programs and CDMO services departments., • Leads with cross-functional stakeholders, including Quality, Legal, Finance, PD / MFG, Supply Chain, R&D, and Eng to execute internal costing, SOW execution and best-in-class customer experience, • Gathers market and competitive intelligence and stays attuned to customer needs / feedback, • Monitors and aligns customer requirements with CDMO capabilities to effectively coordinate and execute on-time program delivery of GMP SOWs., • Develops, communicates, and coordinates improvements in strategy and execution, and provides development for the sales and program management teams to achieve goals, • Provides proactive and in-depth financial analysis to drive sales across CDMO services, • Conducts advanced analysis and business research to report on current and future CDMO services, • Leads strategies for sales promotions, marketing materials, and Maravai / Trilink cross selling, • Needs to be able to work in a fast-paced, multi-tasking environment, • BS in Molecular Biology, Biochemistry, Genomics, or related field (Advanced degree preferred)., • At least 7 to 10 years of relevant work experience in the biopharmaceutical industry, with at least 5 years of sales achievements and customer-facing experience, preferably in a CDMO setting, • Proven ability to sell in complex, multi-stakeholder environments with demonstrable revenue growth achievements and strong indirect leadership capabilities, particularly in influencing and motivating teams to achieve group goals, • Strong people leader with at least 5 years of people management in a commercial related team, • Ability to work independently with 40%+ travel across territories., • Technical background in nucleic acid, gene editing, cell therapy and/ or bioprocessing, • Strong understanding of drug development pathways, GMP manufacturing, and regulatory requirements., • Skilled in Salesforce, MS Office (Word, Excel, PowerPoint); strong presentation and negotiation skills., • Strong communication and presentation skills, • Must demonstrate collaborative work style, with a strong ability to build relationships, gain credibility, and partner with internal customers, • Strong organizational and strategic management skills, • Strong analytic skills in the area of mRNA service programs to provide growth strategies, • Ability to summarize detailed data into an actionable recommendation for a variety of audiences, • Ability to manage multiple projects simultaneously, with great attention to detail #LI-Onsite The benefits of being a #MiracleMaker: • You have the potential to change, improve, and save lives around the world., • You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans., • We offer comprehensive medical plans and HSA/FSA options., • Fertility & family planning assistance., • A variety of additional optional benefits and insurance options, including pet insurance., • Retirement contributions. To view more opportunities to become a #MiracleMaker, visit our career site at Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. Click here to view Maravai LifeSciences Privacy Notice HIRING SCAM ALERT Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that: • Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.), • Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment., • Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment. If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at . If you believe you have been a victim of fraud, you can report this activity at: or .

Job Description About the Role: As an Optician, you will play a critical role in helping patients achieve optimal vision by accurately fitting and dispensing eyeglasses and contact lenses based on prescriptions from ophthalmologists or optometrists. You will ensure that each patient receives personalized care by interpreting prescriptions, taking precise measurements, and advising on lens types and frame styles that best suit their needs and lifestyle. Your expertise will contribute to enhancing patients' quality of life through improved vision and comfort. Additionally, you will manage appointment schedules and maintain detailed patient records to ensure smooth clinic operations. Your compassionate approach and technical skills will be essential in delivering exceptional customer service and fostering long-term patient relationships. Minimum Qualifications: • High school diploma or equivalent., • Completion of an accredited opticianry training program or equivalent experience., • Valid state licensure or certification as required by the United States jurisdiction., • Proficiency in medical terminology related to eye care., • Associate degree or higher in opticianry or related field., • Experience with electronic health records (EHR) and appointment scheduling software., • Strong background in biology or anatomy related to vision and eye health., • Previous customer service experience in a healthcare or retail setting., • Interpret and verify optical prescriptions to accurately fill eyeglass and contact lens orders., • Measure patients’ eyes and facial features to ensure proper fit and comfort of eyewear., • Assist patients in selecting appropriate frames and lenses based on their prescription, lifestyle, and preferences., • Adjust and repair eyeglasses to ensure optimal fit and function., • Manage appointment scheduling and maintain organized patient records., • Provide education and guidance on proper eyewear care and usage., • Collaborate with ophthalmologists, optometrists, and other healthcare professionals to ensure comprehensive patient care., • Handle customer inquiries and resolve any issues related to eyewear products or services., • Submit Claims using Software, • Front Office duties based upon business operational needs The required skills such as manual dexterity and arithmetic are essential for accurately measuring patients and filling prescriptions with precision. Medical terminology knowledge enables clear communication with healthcare providers and understanding of prescriptions. Appointment scheduling and multitasking abilities ensure efficient clinic operations and timely patient care. Compassion and customer service skills are vital for building trust and providing a positive patient experience. Additionally, a foundational understanding of biology supports informed discussions about eye health and appropriate eyewear solutions.

Job Description Sanford Burnham Prebys is much more than a research facility and hub for innovation; it’s a vibrant global community of talented scientists and researchers from over 30 countries. This worldwide representation enriches our perspectives and enhances our creative approach to solving complex scientific challenges. We strive to be leaders not only in biomedical research but also in creating an environment where excellence thrives through collaboration across cultures and backgrounds. Our mission is to advance the biomedical sciences by cultivating the next generation of scientific leaders, providing meaningful opportunities for researchers of all backgrounds to learn, innovate, and make breakthrough discoveries that improve human health. Together, we translate science into health. The duties and responsibilities contained in the job description are intended to be examples of the accountabilities for which the person in the position will demonstrate competency through performance. The job description is not intended to be an all-inclusive list. Duties and responsibilities are subject to change and other duties may be assigned as necessary. Position Summary: This technology role in the institute’s NCI-designated Cancer Center will be responsible for technical execution in the bioinformatics, computational biology and data science spaces. They will be responsible for engineering of complex data-pipelines and associated biostatistical and machine-learning analyses on the outputs of these pipelines. This will include data ingestion, quality-control, feature-extraction, data-visualization, benchmarking and both descriptive and predictive statistical analyses. They will have experience in building and executing data and software pipelines. They will work with a team in identifying technical opportunities, including recognition of new algorithms, datasets and benchmarking opportunities. They may be involved in assembling and submitting funding applications. They may have external-facing roles, including interactions with collaborating research groups, commercial entities and other partner organizations. They will provide technical support to other researchers, including bioinformaticians, statisticians and trainees. They will be expected to generate peer-reviewed scientific research of high-activity, both as a lead and as a collaborator. They will work in a variety of statistical and programming environments including python, Nextflow and R. They will deploy a variety of bioinformatic tools including but not limited to bwa, GATK, MuSE, and delly. They will execute project milestones set by the PI and other internal leaders, and then manage their time and technical skills to achieve those milestones. Amongst their key early roles will be standing up DNA- and RNA-sequencing analysis and benchmarking pipelines for the rapidly-growing Institute cancer data science group. This will involve close collaborations across the Institute, particularly with the Center for Data Science. Duties and Responsibilities: • Modifying, deploying, benchmarking and executing robust, feature-rich Nextflow pipelines, • Performing data-ingestion, data-cleaning and quality-control on biomedical datasets, • Working in a high-performance computing environments, including use of containerization, dev/ops, test-driven development and other software- and cloud-engineering techniques, • Descriptive statistical modeling, • To effectively present results and ideas related to assigned projects both verbally and in writing, • Performs other related tasks, duties and responsibilities as required, assigned, or directed. Experience: • Experience in cancer or genome bioinformatics, • Understanding of DNA and RNA sequencing technologies and algorithms, • At least one (1) year of HPC experience in a containerized environment Other Knowledge, Skills and/or Abilities: · Work independently as well as in a team environment · Be responsible, organized, and a problem solver · Possess strong attention to detail, analytical, time management, organizational, communication, and interpersonal skills · Professional proficiency in Microsoft Office, statistical software and programming · Deep understanding of good software development practices · Fluency in working on HPC environments, particularly those that are containerized Supervisory Responsibilities: Direct: No Indirect: No Compensation: The expected hiring rate for this position is $71,822 - $75,000/annually commensurate with experience. We welcome talented individuals of all backgrounds regardless of gender, sex, religion, race, national origin, citizenship, age, disability, perceived disability, pregnancy, pregnancy-related condition, reproductive health decisions, sexual orientation, gender identity, gender expression, genetic information, HIV/AIDS, marital status, covered veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations. We are proud to be an equal employment opportunity employer. As part of this commitment, Sanford Burnham Prebys Medical Discovery Institute will ensure that persons with disabilities are provided reasonable accommodations for the hiring process. If a reasonable accommodation is needed, please contact our Benefits Team at (858) 646-3100 or via e-mail at

Job DescriptionAs a subject matter expert, this role will support the execution and delivery of clinical and translational biomarker services for Sponsor and internal R&D studies. This role will function to lead and support immunostaining assay development, biomarker projects, and advanced image analysis including developing and applying AI-driven image analysis algorithms to quantitatively assess histopathology and biomarker data, while also serving as a scientific partner to clients from study design through data interpretation and presentation. The role will work cross-functionally with pathologists, laboratory technicians, scientists, project operations and business development teams, and will directly support pharmaceutical and biotechnology clients in planning, executing, and interpreting biomarker studies across preclinical and clinical programs. Responsibilities • Act as a scientific interface with clients, participating in client meetings, protocol reviews and data review meetings, • Provide expert input on design and conduct of clinical or translational studies incorporating biomarker endpoints and “omics and non-omics” techniques including but not limited to immunostaining, proteomics, spatial biology, computational and digital pathology., • Prepare and/or support the preparation and review of project plans, analysis plans and study reports, abstracts, manuscripts, and technical reports., • Partner with laboratory technicians to support immunostaining assay development, optimization, and validation., • Define analytical endpoints, scoring strategies, and quality control metrics aligned with assay performance., • Contribute to assay validation documentation and analytical reports as required., • Develop, validate, and maintain image analysis pipelines for immunostaining (IHC), immunofluorescence (IF), in situ hybridization (ISH), and multiplex assays., • Design and implement AI/machine learning algorithms for tissue segmentation, cell characterization, and biomarker quantification., • Collaborate with pathologists through end-to-end workflows including assay development, validation, quantitative read-outs and interpretation., • Assist with business development activities including participating in client meetings, requests for proposal (RFP) responses, project pricing, protocol review, and bid defenses as needed., • Provide advice to sponsors seeking guidance, • Contribute to continuous improvement of computational, digital pathology, spatial biology and translational research capabilities., • Assist in the development of our product/service platforms to ensure all stakeholder requirements are being considered, documented, and translated to the final solution., • Participate in brainstorming meetings and functionality reviews.Qualifications, • Post-graduate degree / professional designation; 7-9 years related experience, plus continuous training and knowledge/skills upgrading, • Strong experience with digital pathology and image analysis, • Solid understanding of histopathology and immunostaining techniques, • Experience working in CRO, laboratory, biopharma and/or regulated research environment, ideally supporting clinical and translational research studies, • Experience presenting data to external stakeholders or at scientific meetings, • Scientific rigor and attention to detail - able to communicate complex scientific concepts and results clearly to all stakeholders, • Strong written and oral English communication skills, problem-solving and analytical thinking

Job DescriptionCapricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most. As a Manufacturing Associate I, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trials and exosome development, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success. Responsibilities • Perform routine manufacturing tasks, including media preparation, cell culture, cell counting, formulation, centrifugation, and freezing., • Complete and ensure timely, accurate documentation in compliance with GMP standards across batch records, forms, and protocols., • Mentor fellow team members on cGMP documentation protocols to ensure the highest standards., • Plan, collect, analyze, and report on production data, maintaining comprehensive records and observations., • Author, revise, and maintain SOPs through Capricor’s document change system., • Oversee inventory, material transfers, and cleanroom procedures to support efficient GMP operations., • Prepare technical summaries, protocols, and reports to ensure full documentation of production activities., • Lead moderate-complexity CAPAs and assist with deviations and investigations to maintain quality assurance., • Take on special projects in manufacturing and development as required.Requirements, • Bachelor’s degree in Biomedical Engineering, Biological Sciences, or a related field., • 1-3 years of experience in a cGMP/cGTP manufacturing environment., • Solid laboratory experience in mammalian tissue culture, along with expertise in aseptic techniques., • Working knowledge of regulatory standards in biopharmaceutical or tissue banking industries., • Strong organizational skills and acute attention to detail within a fast-paced, dynamic setting., • Basic molecular biology and flow cytometry skills are a plus. Notice to Recruiting Agencies Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.

Job DescriptionCapricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most. As a Manufacturing Technician, you’ll be a vital part of Capricor’s efforts in delivering therapies for patients in need. Supporting critical clinical trialscommercial production, you’ll perform meticulous production tasks and documentation to uphold our quality and compliance standards. This role places you in a cleanroom environment, where precision and attention to GMP standards are essential. You’ll be instrumental in ensuring that each production step is performed with accuracy, ultimately contributing to Capricor’s therapeutic success. This role is a full time position on our Manufacturing team, this position will be a 2-2-3 work schedule. Responsibilities • Maintaining cleanroom inventory, performing material transfers and cleanroom-required activities to support cGMP operations (i.e restocking Kanban, scrubs, and gowning), • Ensuring clear communication and working closely with manufacturing and materials management to confirm proper materials are stocked accordingly;, • Performing cleanroom setup and shutdown (Biohazard waste decontamination, packaging and autoclaving of required materials/supplies, etc), • Performing special manufacturing projects, • Completing required documentation with proper cGMP recording of entries and comments on batch records, forms and protocols independently;, • Operation, Maintenance, and Cleaning of GMP equipment, including: Centrifuges, Microscopes, Incubators, BSCs, Refrigerators, Freezers, etc, • Initiate minor revisions to existing documents, to troubleshoot simple existing procedures, and to contribute to continuous improvement initiatives., • Performing such other duties as may be assigned from time to time. Requirements, • High school diploma or GED required, • Bachelor’s degree in Biology, Biological Sciences or related field preferred, • 0-1 years of experience in cGMP/cGTP manufacturing environment in academic/industry setting, • Lift, push, pull and carry up to 40 lbs., • Excellent knowledge of aseptic technique and aseptic practices, • Excellent knowledge of Good Documentation Practices, • Exceptional communication and interpersonal skills, • Excellent organizational skills and attention to detail, • Excellent interpersonal skills, team player, • Ability to work in a dynamic environment, • Adaptable/flexible with work schedule with an ability to multi-task and prioritize work, • From time-to-time extended hours may be required with or without notice, dependent on the work needed Notice to Recruiting Agencies Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without expressed consent from Talent Acquisition management and a prior written agreement. Agencies that contact hiring managers directly, solicit business, or submit candidates without this approval will not be considered for any engagement. All such submissions become the property of Capricor Therapeutics, and no fees will be paid for any candidates hired as a result. We appreciate your cooperation and respect for this policy.

Ideal Participants May Hold Titles Such As - Earth Science Professor - Atmospheric Science Instructor - Marine Biology Lecturer - Oceanography Faculty - Geoscience Teacher - Climate Science Educator Requirements - Master's degree or higher in Earth Science, Atmospheric Science, Oceanography, Geolog

Ideal Participants May Hold Titles Such As - Earth Science Professor - Atmospheric Science Instructor - Marine Biology Lecturer - Oceanography Faculty - Geoscience Teacher - Climate Science Educator Requirements - Master's degree or higher in Earth Science, Atmospheric Science, Oceanography, Geolog

The Associate Director, Field Marketing, is a field-based, customer-facing (non-sales) role and a key member of the Dermatology marketing team. Bachelors degree required, preferably in biology, marketing, strategy, or business administration. Share synthesized customer insights with cross-functional

Bachelor degree with 0-3 years of professional experience in molecular biology, biotechnology, or biochemistry required. Proficiency in molecular biology techniques, including DNA/RNA extraction & purification, NGS library preparation & QC, PCR, qPCR, cloning, etc. The Sequencing Research & Genomics

Job Description Data Analyst 1 year San Diego, CA Database entry or management experience (1+ year) Microsoft Excel ERP (1+ year hands-on experience preferred) Jet Report/Power BI SQL (or an understanding of if/then logic-based statements) PIM/MDM (preferred) Attention to detail, critical thinking Works well in a team environment, good communication Knowledge of the biotech industry, biology, and/or immunology (preferred) Knowledge of manufacturing practices and bills of material (preferred) Education: Bachelor's degree (completed or completing soon) in any major (focus on data or biology preferred) Knowledge of the biotech industry, biology, and/or immunology (preferred) The Database Assistant will provide operational support for day-to-day business activities for the Product Release Team (PRT) and Product Data Supervisor. This would include assignment of item/catalog numbers, as well as input and maintenance of relevant data in the ERP system. They will also provide technical support to perform data analysis and preparation that contribute to our data reporting and overall data integrity. The individual will help ensure that all item-related data is available in the necessary systems and legal entities. Lastly, the Database Assistant will also help with process improvement and automation initiatives. #TB_PH #ZRCompany DescriptionFounded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX & downtown San Francisco, CAFounded in 2002 by three former Monster.com executives; TalentBurst is an award-winning full-service Staffing Firm working directly with Fortune 500 companies in the US and Canada. We specialize in Contract and Contract to Permanent roles across many industries and have direct/contractual relationships with all our clients. Please visit our website or come meet us at our offices in Natick, MA, Miami, FL, Christiansburg, VA, Vineland, NJ, Houston, TX & downtown San Francisco, CA

Job DescriptionSalary: $52,500 to $57,500 per year DOE Ideal Candidate Profile Do you fit this profile? • Wants to start a CAREER / not just another "job", • Wants to make a difference, • High Moral Standards & Values, • Positive, • Helpful, • Team Player, • Professional, • Wants to be the best of the best, • Is Ready Envirocheck is a growing company and has exciting opportunities for A players on our team. Job Summary Our environmental field technicians / consultants (level 1) provide clients with advice regarding potential contaminant presence in a variety of settings including residential, commercial, and industrial buildings. An ideal candidate should be an individual who is self-motivated, this hands-on position requires strong analytical and communication skills to identify a potential issue and convey the said issue to a client with remedial solutions when necessary. Through on-the-job training and certification courses, field technicians gain knowledge regarding state and federal regulations and in turn conduct surveys and produce reports as a knowledgeable party. The successful candidate for this position will have the opportunity to advance to Level 2 and Level 3 with the potential to earn a base salary of $65,000+ per year by 1 year of hire, and $72,500+ per year by 3 years of hire. As knowledge, experience, and capabilities increase, additional levels may become available. Responsibilities and Duties • Conduct on-site inspections, which includes documentation of site conditions, sampling, and in-person consultation, • Produce professional survey reports based on inspection notes and sample data with remedial recommendations as necessary, • Coordinate with multiple parties regarding inspections while keeping all parties best interests in mind, • Adhere to all applicable state and federal laws and regulations and communicate that information to clients in a professional manner Qualifications and Skills • No experience required - will train., • High school diploma is required., • Prefer individuals with a bachelor's of science degree in construction management, biology, chemistry, environmental science, and/or a related science., • Valid Driver's License, • We are hiring for all levels! Certified asbestos consultants (CAC), certified site surveillance technicians (CSST), Lead sampling technicians, or CA DHS lead inspector/assessors are encouraged to apply. Benefits • Health Insurance options, • 401K with matching, • Company vehicle & iPhone & gas card provided, • Paid Training & Field-Related Education