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Tutor Map are offering new tuition and teaching positions in Carlsbad.We are seeking Biology tutors and teachers in Carlsbad.You can register for free, we take zero commission.Tutor Map is the largest online tutoring company in the UK and are expanding to the US.We have been running for over 18 year

Job Description Corporate Overview Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence. Pay Range Pay range for this position is $20.00 - $26.00 per hour, depending on experience. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. This is a temp to hire position. Position Overview The Manufacturing Technician II/III is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% On-Site, Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Start time for this position is 12:00 pm with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties * Ability to work within an ISO 13485 and cGMP production environment and ensure compliance with our quality system. * Execute documentation based on cGMP and GDP procedures, as well as perform documentation review post manufacturing execution. * Participate in Quality Working Teams and Continuous Improvement Teams. * Visual inspection of lyophilized product and heat seals of packaging. * Clean and sanitize manufacturing and associated support areas. * Responsible for monitoring machinery and reporting alarms to lead technician or Supervisor. * Conduct daily documentation review. * Participate in Quality Working Teams and Continuous Improvement Teams. * Operate large machinery and monitor automated. * Employee may be required to manage hazardous wastes in compliance with company procedures & State/Federal/Local hazardous waste regulations. Duties may include identifying, handling, generating, accumulating, storing, labeling, and on-site transporting of hazardous wastes. * Perform daily arithmetic calculations as it pertains to total volume and liquid concentrations. * Perform daily unit conversions as it pertains to gravimetric and volumetric measurements. * Operate production equipment such as pipettes, balances, pH meter and heat sealers. * Monitor department equipment for proper operation that is within calibration. * May perform safety and cGMP inspections or observations. * Ensure compliance with SOP/cGMP and cGDP requirements. * Assist in training/ leading of new team members in production activities. * Assist in updating and new revision of standard operating procedures (SOP). * May need to be an author for any MFG Non-Conformance Reports (NCR) and risk analysis memos. * Receive and distribute supplies into the production area as necessary. * Perform NetSuite transaction, issue material, completion and closing of work orders. * May assist with review of quality assurance logbooks. * May perform other duties as assigned. Education Requirements Level II * Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with at least 1 year of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field; or High school diploma/equivalent with 3+ years of related manufacturing experience in a cGMP environment. Level III * Bachelor's degree in a related field (Biotechnology, Molecular Biology, or Biochemistry) with 2+ years of work experience at Argonaut or in manufacturing within a cGMP environment; Associate's degree in a related field with 3+ years of related experience; or High school diploma/equivalent with 5+ years of related manufacturing experience in a cGMP environment. Required Skills and Knowledge * Punctuality and reliable attendance required. * Ability to read and follow detailed written instructions; strong verbal and written communication skills. * Proficient in reading, writing, and conversing in English to understand cGMP manufacturing processes and SOPs. * Knowledge of manufacturing production processes related to product integrity, including visual inspection of components and finished goods, manual and semi-automated packaging, and product labeling. * Understanding of basic chemical and biological safety procedures. * Basic knowledge of formulation, filling, and kitting operations and capabilities. Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US. Background checks are conducted to support workplace productivity, safety and security by ensuring applicant backgrounds and qualifications are suitable for the position being considered. It is the policy of Argonaut Manufacturing Services, Inc., as part of its hiring procedures, to conduct background checks on finalist(s) for all positions. These checks will be job-related, consistent with business necessity and conducted pursuant to all applicable laws, rules, policies and procedures. Background checks may include, but are not limited to: verification with educational institutions or licensing/credentialing boards; standard criminal checks, employment verification; and other pertinent information and resources. Employment offers will generally be made after successful completion of applicable background check(s). However, any offers of employment made prior to completion of the background check(s) shall be contingent upon successful completion of the check(s). Finalist(s) may be rejected if they provide inaccurate, untruthful information, don't fully participate in a required background check, or don't sign or complete a required form.

Job DescriptionRare opportunity to learn and grow with our company! Liberty EnviroLab is currently seeking Full Time Experienced Laboratory Analysts specializing in wildfire, structure fire, asbestos, and mold analysis. Liberty EnviroLab is located in San Marcos in the northern San Diego County. Liberty offers a variety of analytical testing services to support environmental investigations focused on wildfire, structure fire, asbestos, mold (microbiology). Our management team has over 71 years of combined experience in particulate analysis and trace evidence examination. We believe in empowering our customers with accurate and defensible analytical results. Some Responsibilities Include: Safely perform analyses on samples according to Libertys Standard Operating Procedures (SOPs) using advanced instruments. Follow all laboratory QA/QC requirements Record data using computer software and programs. Maintain equipment according to manufacturer guidelines and company procedures. Perform other assigned duties, as requested by supervisor. Requirements: Associates or Bachelors Degree in a life science (biology, chemistry, environmental science, etc.) preferred. 1-2 years of Polarized light microscopy (PLM) experience required. 1 year of Phase contrast microscopy (PCM) experience required. Self-motivated, independent, and team oriented. Must be able to work in a fast-paced setting, multi-task, and prioritize assignments. Good communication, computer, typing, and organizational skills. Liberty EnviroLab offers full time benefits: medical, 401k, sick pay, paid time off, and holiday pay. Pay range for this position is $22.00-$29.00 per hour. The work schedule is flexible. Visit our website for more information about our company. Please submit your resume, or call us at 760-539-7024 for assistance!

Job Description Job Overview: An established medical device manufacturer is seeking a Quality Control Technician to join its Chemistry team. This role is responsible for performing quality control testing on products throughout various stages of production, supporting core QC functions, and ensuring accurate documentation. Ideal candidates are detail-oriented, collaborative, and comfortable working in a regulated lab environment. Responsibilities: • Perform and document QC Sofia Testing on in-process and final production lots, • Conduct 1st article functional testing for Sofia Final Kits, • Support QC Chemistry functions including stability studies, raw material testing, and complaint investigations, • Assist with product development and improvement projects, • Maintain lab cleanliness and organization, • Operate lab equipment safely and in accordance with SOPs, • Collaborate with cross-functional teams including Manufacturing, R&D, and Quality Engineering, • Bachelor’s degree in Chemistry, Biology, Life Sciences, or equivalent experience (preferred), • 0–2 years of experience in a QC or manufacturing lab environment, • Experience in medical device or high-volume manufacturing (strongly preferred), • Familiarity with QSRs/ISO, GLP/GMP, and basic quality concepts, • Strong written and verbal communication skills, • Proficient in Microsoft Office and data entry tools, • Lab, office, and manufacturing settings, • Exposure to biological and chemical hazards, • Ability to lift up to 20 lbs and work at a lab bench or desk for extended periods Apply Now If you're ready to contribute to healthcare innovation and work in a fast-paced, quality-driven environment, we encourage you to apply today!

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. We will invest in two weeks of paid training to prepare you to pass your RBT exam. 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 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 at MeBe’s Learning Center. * 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 * 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 Description About the Role The Assay Scientist plays a key role in advancing research and development initiatives focused on genomic technologies and molecular diagnostics. This position combines hands-on laboratory experimentation with data analysis to support the development of innovative genomics-based assays and products. The ideal candidate will have experience in NGS, bioinformatics, and cancer genomics, with a strong drive to contribute to translational research and product development in clinical and research applications. Responsibilities * Lead research projects to validate genomic technologies for detecting genomic rearrangements in clinical and translational applications * Design and implement development plans for future genomics-based products, services, and applications * Perform molecular biology and genomics experiments, including sample preparation, sequencing, and assay optimization * Analyze high-throughput genomic data using standard and custom bioinformatics tools * Interpret experimental results and propose actionable next steps to cross-functional stakeholders * Collaborate with internal teams including R&D, bioinformatics, and product development to support project goals * Engage in technical discussions with external collaborators and scientific partners * Monitor scientific and technological trends in cancer diagnostics, genomics, and molecular biology * Deliver internal technical presentations and contribute to departmental knowledge-sharing sessions * Represent the team by presenting research findings at external scientific meetings and conferences * Identify potential challenges in research projects early and implement solutions or escalate appropriately * Participate in regular lab and R&D team meetings, promoting a collaborative and innovation-driven environment * Support additional projects and initiatives as assigned Qualifications * PhD or MS in Molecular Biology, Genomics, Bioinformatics, Biochemistry, or related field * Hands-on experience with next-generation sequencing (NGS) workflows and data analysis * Proficiency in using bioinformatics tools and scripting languages (e.g., Python, R, Bash) * Strong understanding of genomic rearrangements, chromatin biology, and cancer genomics * Proven ability to interpret and present complex genomic data to diverse audiences * Experience working in cross-functional research or development teams * Excellent written and verbal communication skills * Demonstrated ability to manage multiple projects and meet deadlines Desired Qualifications * Experience with Hi-C or chromosome conformation capture technologies * Familiarity with clinical assay development or regulatory standards for molecular diagnostics * Background in technology transfer or product commercialization * Publication record in peer-reviewed scientific journals * Experience presenting at national or international scientific conferences * Knowledge of single-cell genomics or spatial transcriptomics * Previous involvement in industry academic collaborations

Job DescriptionJob Title: Research Associate Job Description We are seeking a dedicated Research Associate to join a dynamic team, working primarily on bench-based molecular biology techniques. This role involves performing DNA extractions from blood, conducting PCR and sequencing (including n-point PCR or r-PCR), and applying aseptic techniques. The ideal candidate will follow standard operating procedures meticulously and document their work with precision. This position offers opportunities to learn and apply molecular techniques in an automated process and to work collaboratively within a specialized biotech team. Responsibilities • Perform DNA extractions from blood samples using aseptic techniques., • Conduct PCR and sequencing procedures, including n-point PCR or r-PCR., • Follow and document standard operating procedures (SOPs) accurately., • Create and manage bench controls, performing tasks that may vary in time commitment from half a day to two weeks., • Collaborate with the platform integration team and cross-functional teams during different project stages., • Solve problems effectively and communicate efficiently within the team., • Proficiency in GLP, PCR, DNA extraction, and aseptic techniques., • Experience with nucleic acid techniques, including purification and quantification., • Familiarity with molecular biology, including sample preparation using magnetic particles., • Competency in data interpretation and analysis., • Experience with standard laboratory techniques in a BSL-2 environment is a plus., • Bachelor's degree in Molecular Biology, Biochemistry, Microbiology, Chemistry, or Immunology with 1.5 to 3 years of relevant experience., • Proficiency in Microsoft Office Suite (MS Word, Excel, PowerPoint). This position is part of a seven-member integration team within a larger group of 17 professionals. The role is predominantly lab-based, requiring 90% of work time on bench tasks. The work schedule is flexible with an 8am-5pm timeframe, with a preference for earlier starts. The company culture is supportive, fostering a kind and personable atmosphere, and accommodating flexible work needs. Pay and Benefits The pay range for this position is $26.00 - $33.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in CARLSBAD,CA. Application Deadline This position is anticipated to close on Oct 3, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

Job DescriptionSalary: $27-$45 Hourly (DOE) RESPONSIBILITIES • Completing daily health assessments prior to starting each workday., • Conducting daily safety self-meetings using a Pangea-approved app., • Submitting daily safety check-in/check-out texts to Pangeas team., • Reviewing project documents and evaluating environmental requirements related to the projects., • Conducting daily field inspections to ensure environmental compliance., • Performing biological surveys, nest surveys, nest sweeps, andstormwater inspections., • Assist with stormwater sampling as needed., • Composing and submitting accurate and thorough daily inspection reports (with photographs) for submittal to clients, and state and federal agencies., • Uploading project photographs to Pangeas cloud server daily., • Apply excellent communication skills with project team, landowners, clients, construction, and the public., • Identifying issues and concerns and determining appropriate resolutions, while working collaboratively with Pangeas management team., • Conducting training and providing environmental updates to crews during daily tailboards., • Coordinating with construction teams to determine schedules and planned work activities to evaluate areas before construction., • Meeting with construction personnel to assess project access, extra work areas, and deviations from project plans to complete Field Change Orders (FCOs)., • Attending meetings with Pangeas internal team to discuss compliance status., • Providing daily and/or weekly email summary updates to Pangeas team regarding project concerns and needs., • Collaborating with the Pangea team to provide details and input for weekly reports., • Coordinating with Pangeas team regarding environmental compliance, including challenges, observations, and solutions., • Recording real-time entry of time (clocking in/clocking out with Pangea-approved app on company-provided iPhone), ensuring lunches and breaks are accounted for within the app., • Submitting mileage and vehicle service needs via email or smartphone app according to a schedule defined by Pangea., • Performing other duties as assigned. QUALIFICATIONS • Bachelors degree in Environmental Science, Wildlife Management, Sustainability, Biology, Ecology, or a related field. Demonstrating a solid educational foundation, this role requires a relevant degree., • Minimum of 4 years of experience in biological/environmental monitoring or compliance roles: Candidates must showcase proven expertise and bring substantial hands-on experience navigating complex environmental landscapes effectively, in California, and the western United States., • Proficiency in Microsoft Office Suite (Word, Excel) and Google Earth: Essential technical skills are required to understand and analyze data accurately, ensuring precision in reporting, with secure and reliable high-speed internet service., • Strong knowledge of environmental regulations and compliance requirements specific to California: Comprehensive regulatory knowledge - Environmental Compliance Inspector/Monitor will ensure all projects adhere to state and federal environmental standards., • Excellent communication skills: Effective communication with team members and stakeholders with timely, effective, and respectful communication., • Ability to manage multiple tasks concurrently while maintaining attention to detail: Multitasking should not compromise quality; the Environmental Compliance Inspector/Monitor must juggle various responsibilities while focusing on detail-oriented execution., • Experience conducting fieldwork, environmental monitoring, and other environmental surveys: Field-ready expertise is crucial for accurate data collection, compliance assessments, and fostering environmental stewardship., • Problem-solving mindset with a proactive approach to addressing issues: Environmental Compliance Inspector/Monitor must anticipate challenges and devise strategic solutions promptly, ensuring seamless project progress., • Ability to work independently and as part of a team in a fast-paced environment: Flexibility and teamwork ensure adaptability in project environments, fostering collaborative efforts., • High personal integrity, professionalism, and business ethics: Upholding the highest standards, the Environmental Compliance Inspector/Monitor must demonstrate honesty, reliability, and ethical behavior in all aspects of their work., • Strong work ethic strive for excellence, accuracy, and efficiency: Dedication to achieving superior results underscores our commitment to quality and thoroughness in every task., • Proactive and positive even when challenges arise: Maintaining optimism and forward-thinking solutions ensures resilience and effective problem-solving under pressure., • Ownership in the role and with assignments, fully accountable for success: Taking responsibility for ones duties and outcomes reinforces accountability., • Quick learning and accurate following of directions: Rapid adaptation to new information and precise execution of instructions are vital for maintaining high standards and efficiency., • Resourceful mindset, anticipating issues with solutions at the ready: Foreseeing potential obstacles and preparing actionable solutions exemplifies resourcefulness., • Ability to manage last-minute changes and reprioritize: Flexibility in the face of shifting priorities maintains project momentum., • Taking appropriate follow-up actions: Taking necessary follow-up actions ensures that all tasks are completed thoroughly and responsibly. COMPENSATION AND BENEFITS • Pay range: $27.00-$45.00 per hour, • 401(k) program with company matching, • Employee Assistance Program (EAP) (company-paid), • Flexible Spending Account (FSA), • Health Insurance available after 30 days of employment (company contribution, eligibility requirements), • Dental Insurance is available after 30 days of employment (company contribution, eligibility requirements), • Vision Insurance available after 30 days of employment (eligibility requirements), • Health Savings Account (HSA) & Flexible Spending Account (FSA) (eligibility requirements), • Life insurance is available after 30 days of employment (company-paid), • AD&D available after 30 days of employment (company-paid), • Accident insurance available after 30 days of employment (eligibility requirements), • Critical illness insurance is available after 30 days of employment (eligibility requirements), • Hospital indemnity insurance available after 30 days of employment (eligibility requirements), • Supplemental life insurance and AD&D available after 30 days of employment (eligibility requirements), • Vacation & Holiday Pay (eligibility requirements), • Sick Time, • Eligible for Discretionary Bonus and other Perks, • Professional Development Opportunities, • Wellness Program, • Referral Program TRAVEL This position requires local day travel and possible overnight travel for temporary field assignments, with travel, lodging, and meals paid. WORK ENVIRONMENT The Environmental Compliance Monitor/Inspector works remotely at home and outside in the field. This position requires frequent use of four-wheel-drive vehicles. PHYSICAL DEMANDS The physical demands described in this job description are representative of those that must be met by an employee to successfully perform the essential job functions of this role. While performing the duties of this job, the Associate Biologist is required to: • See, talk, hear, read, write, walk and stand for a minimum of 1 hour up to 12 hours a day sometimes on uneven or rocky terrain, while bending, crouching, and reaching to collect data, and hiking several miles per day to conduct surveys and/or monitor construction activities., • To work in the field for long hours., • May be exposed to inclement weather including rain, snow, and hot and cold temperatures., • Must be able to carry or lift up to 35 pounds., • Must wear protective equipment such as; gloves, hardhat, safety glasses, ear protection, safety vest, reinforced-toe boots, snake chaps, long sleeves, and long pants., • May be exposed to thick brush, poison oak, snakes, and insects when working outside in the field. SCHEDULE Monday to Friday (weekend work possible, at times, due to client schedules) WORK LOCATION • Southern California, • Other locations and opportunities available outside of San Diego County (in Southern California and the western U.S.)

Job Description About the Role: The Vice President Bioinformatics and Software Engineering will provide strategic and technical leadership for computational biology, software development, and data infrastructure in support of whole genome sequencing (WGS), multi-omics analysis, and clinical diagnostics. This executive role requires deep expertise in de novo algorithm development, data modeling, and scalable bioinformatics methods for genomic discovery and precision medicine. The successful candidate will lead a multidisciplinary team of bioinformaticians and engineers, advancing both production-ready clinical pipelines and cutting-edge computational research to enable next-generation diagnostics. Responsibilities: * Develop and execute the strategic roadmap for bioinformatics and software engineering, with emphasis on de novo method development and novel algorithm design. * Lead the design, validation, and deployment of NGS pipelines for WGS, RNA-seq, and multi-omics applications, ensuring compliance with CLIA, CAP, and FDA standards. * Drive innovation in data modeling, statistical methods, and computational frameworks to address large-scale genomic and structural variation analysis. * Oversee end-to-end software engineering efforts including cloud infrastructure, APIs, automation tools, and scalable production systems. * Establish and enforce engineering best practices in version control, testing, reproducibility, and audit-ready documentation. * Recruit, mentor, and manage a high-performing team spanning bioinformatics, machine learning, software engineering, and data science. * Collaborate with R&D, Clinical, Regulatory, and Product teams to integrate novel computational methods into diagnostic product development. * Shape the data strategy to support AI/ML applications, real-world evidence generation, and advanced data integration across omics modalities. * Ensure compliance with data security, privacy, and regulatory frameworks across all systems and workflows. * Foster partnerships with academic, industry, and open-source communities to accelerate innovation in bioinformatics methods and software solutions. Qualifications: * PhD or MS in Bioinformatics, Computational Biology, Computer Science, or a related discipline. * At least 10 years of experience in bioinformatics and software engineering, with proven expertise in algorithm development for NGS and large-scale genomics. * Demonstrated success in developing de novo methods for genome assembly, structural variant detection, or advanced computational modeling. * Strong track record building cloud-based platforms and production-grade pipelines for regulated diagnostics. * Leadership experience managing cross-functional teams across bioinformatics, engineering, and clinical domains. * Deep understanding of regulatory compliance frameworks including CLIA, CAP, and FDA submissions. * Hands-on expertise with cloud infrastructure, distributed computing, and data-intensive systems, preferably AWS. * Exceptional communication skills, with the ability to influence technical, scientific, and executive stakeholders. Desired Qualifications: * Experience with multi-omics integration, statistical modeling, and advanced algorithmic methods in computational biology. * Background in genome assembly, haplotype phasing, structural variant calling, or other de novo discovery pipelines. * Familiarity with LIMS, clinical reporting systems, and laboratory automation workflows. * Experience leading FDA submissions and developing QMS-aligned software systems for diagnostics. * Knowledge of AI/ML applications in bioinformatics, including predictive modeling and real-world data analysis. * Proven ability to translate computational innovations into clinically validated products.

Lead Auditor / Assistant Director, GMP Quality Systems Workplace: Carlsbad, CA (on-site preferred) or remote (quarterly travel required, expenses covered) Salary range: $100,000–$140,000 + 15% performance bonus + equity (RSUs & stock options) About the Company Our client is a commercial-stage biotechnology company recognized for pioneering RNA-targeted medicines and advanced gene technologies. With multiple approved therapies, a robust pipeline, and a shift toward commercial GMP operations, the company is expanding its Quality Systems team to ensure global inspection readiness and regulatory excellence. Position Overview We’re seeking an experienced GMP Auditor to step into a strategic Assistant Director-level role within our Quality Systems and Vendor Management team. Reporting to the Director of GxP Quality Systems, you will own and elevate the Internal Audit Program while supporting GMP vendor management. This is a high-impact, individual contributor role—ideal for someone who thrives on leadership through influence, program ownership, and cross-functional collaboration. Key Responsibilities • Lead and modernize the Internal Audit Program:, • Conduct risk-based audits of internal GMP functional areas., • Transition the program beyond compliance checks to a holistic, risk-driven model., • Ensure inspection readiness for commercial operations., • Conduct hands-on audits with emphasis on:, • Computer System Validation (CSV) & Data Integrity, • Drug product fill/finish processes, • Combination products (e.g., auto-injector assembly), • Vendor Management:, • Perform GMP vendor qualification, ongoing audits, and performance monitoring., • Oversee Quality Agreements, Change Notifications, and vendor-related CAPAs., • Partner with stakeholders to drive vendor compliance and continuous improvement., • Stakeholder Collaboration:, • Work cross-functionally with QA, manufacturing, and global quality partners., • Influence teams to recognize risks, strengthen systems, and drive enhancements., • Quality Leadership:, • Demonstrate ownership, initiative, and strong communication skills., • Serve as a quality culture ambassador—driving agility, compliance, and continuous improvement. Qualifications Required: • Bachelor’s degree in a Life Sciences field (Chemistry, Biology, Biotech, Engineering, etc.)., • 8+ years’ experience in life sciences or pharma, with at least 5 years focused on GMP auditing/vendor management., • Strong knowledge of global GMP regulations (FDA, EMA/Eudralex, ICH, MHRA, Health Canada, etc.)., • Proven experience with CSV audits, data integrity, and drug product fill/finish., • Ability to lead programs independently, influence stakeholders, and communicate effectively at all levels., • Track record of working in mid-to-large pharma/biopharma environments (preferred over small biotech only). Preferred: • Experience with antisense oligonucleotide manufacturing., • Exposure to combination product/device assembly., • Familiarity with electronic audit systems (e.g., TrackWise, Veeva)., • Continuous improvement mindset with demonstrated program-building skills. Why Join Us • Be part of a growing Quality Systems team shaping the company’s commercial readiness., • Work in a collaborative, global, and innovative environment with colleagues across the U.S. and Europe., • Competitive compensation package: base + annual bonus + equity., • Flexibility: onsite in Carlsbad preferred, but remote considered for strong candidates (quarterly travel required, fully covered).

Job description PhD Scientific Director/Grant Writer: Must have a proven immuno-oncology track record in Biotech with winning major preclinical and clinical stage grants. Must have a background in oncology/hematology/cell therapy Targazyme, Inc. is a San Diego based, clinical stage biopharmaceutical company developing novel enzyme-based platform technologies and products to improve clinical efficacy, safety and cost of care outcomes for stem cell medicine, immunotherapy for cancer and autoimmune diseases, gene therapy and regenerative medicine. Targazyme is entrepreneurial and fast-moving in nature and desires additional team members with similar qualities. With a FDA SPA in place, our medium term goal is to become a public company, driving global Phase 3 registration trials towards product approvals. Primary Responsibilities: • Generates and delivers multible winning grant applications monthly, drive achievement of major funding to advance our science - fucosylation enzymes to transform outcomes for patients undergoing cell therapy., • Initiate and work with academic labs and opinion leaders to form collaborations and discovery efforts as part of grant submissions, including managing and executing on all grant-related activities, • Manage efforts in lead optimization, transition into pre-clinical development, and oversee pre-clinical studies, • Work closely with the development team, in house or outsourced, ensuring effective coordination of all pre-clinical projects as well as contributing to clinical trial activities Desired Skills, Experience and Qualifications: • Grant Writer with proven track record in winning major pre-clinical and clinical grants, both government and foundation-related mechanisms. Proven as an effective PI - able to deliver on project milestones with limited resources., • Ph.D. or M.D. with strong background in hematology/oncology, immunology, organ/cell transplantation, in-depth knowledge of the drug development and approval process; experience in drug research and clinical development; and experience and expertise in a wide range of molecular biology, biochemistry, and cell biology techniques, • Capable of being Principal Investigator (PI) on clinical trial grants. Proven track record with driving multiple collaborators together to put together winning grants within compressed timeframes with winning quality. Track record of winning major grants and also delivering on milestones with quality, on time and within budget., • Proven track record in designing and executing new research project initiatives and delivering positive results and meeting project milestones. Strong skills in project management, data documentation, problem solving and trouble-shooting., • Must be entrepreunerial, multi-tasking, fast-paced, resourceful and able to overcome obstacles independantly. Strong drive for excellence. Must have the ability to be strategic and tactical at the same time and be execution and results-oriented. Ability to focus on important details, exhibit flexibility, am highly responsible, takes feedback well and respond effectively. Compensation: Initial compensation will be stipends received from awarded grants, equity and bonuses. Post new grant awards &/or Closing of Targazyme's Pre-IPO Mezzanine Financing Round, competitive Pre-IPO Company compensation commensurate with experience, includes equity Contact Information: Lynnet Koh

Digital Pathology Technician Onsite, Vista CA 92081 W2 Contract to Possible Hire The Digital Pathology Technician – AI/ML Support is a key technical role supporting our mission to advance cancer diagnostics through innovative digital pathology solutions. This role combines expertise in digital imaging, histological slide handling and close collaboration across laboratory, engineering, and data science teams. In this role, you will help ensure the accuracy, consistency, and quality of scanned slides used in digital workflows and data-driven applications. You’ll support continuous improvement in slide preparation, scanning, and artifact handling processes, helping enable scalable, high-quality datasets. This position reports to the Manager, SW Developer and is based on-site. In this role, you will have the opportunity to: • Procure, order, organize, and track tissue blocks and histology slides to support digital scanning workflows., • Prepare and load slides for whole slide imaging, ensuring high-quality scans through proper calibration and scanner maintenance., • Perform quality control (QC) on scanned slides, identifying and annotating scan-related or histological artifacts according to defined protocols., • Collaborate with pathologists and lab staff to define, refine, and continuously improve artifact classification and annotation workflows., • Partner with cross-functional teams, including Machine Learning (ML) and Data Science, to align on image quality standards, annotation guidelines, and model training requirements., • Contribute to best practices for digital pathology operations and cross-functional workflows between lab and data science teams. The essential requirements of the job include: • Hands-on experience with digital slide scanners (e.g., Leica, Hamamatsu, Aperio), including basic imaging calibration and maintenance., • Experience working with digital pathology or lab information systems (LIS/LIMS)., • Strong attention to detail with the ability to follow and optimize standardized protocols., • Effective communication and collaboration skills across technical and non-technical teams. It would be a plus if you also possess: • Associate’s or Bachelor’s degree in Histotechnology, Biology, Medical Laboratory Science, or a related field., • 1–3 years of experience working in a histology or pathology laboratory., • Knowledge of histological processes including sectioning, staining, and slide preparation., • Prior experience with digital annotation platforms (e.g., QuPath, or internal tools)., • Experience working in a regulated environment with exposure to CAP/CLIA or IVD workflows., • Understanding of how slide quality and annotation accuracy impact machine learning performance., • Experience in digital pathology workflows and image quality control for AI/ML or research applications.

Digital Pathology Technician Onsite, Vista CA 92081 W2 Contract to Possible Hire The Digital Pathology Technician – AI/ML Support is a key technical role supporting our mission to advance cancer diagnostics through innovative digital pathology solutions. This role combines expertise in digital imaging, histological slide handling and close collaboration across laboratory, engineering, and data science teams. In this role, you will help ensure the accuracy, consistency, and quality of scanned slides used in digital workflows and data-driven applications. You’ll support continuous improvement in slide preparation, scanning, and artifact handling processes, helping enable scalable, high-quality datasets. This position reports to the Manager, SW Developer and is based on-site. In this role, you will have the opportunity to: • Procure, order, organize, and track tissue blocks and histology slides to support digital scanning workflows., • Prepare and load slides for whole slide imaging, ensuring high-quality scans through proper calibration and scanner maintenance., • Perform quality control (QC) on scanned slides, identifying and annotating scan-related or histological artifacts according to defined protocols., • Collaborate with pathologists and lab staff to define, refine, and continuously improve artifact classification and annotation workflows., • Partner with cross-functional teams, including Machine Learning (ML) and Data Science, to align on image quality standards, annotation guidelines, and model training requirements., • Contribute to best practices for digital pathology operations and cross-functional workflows between lab and data science teams. The essential requirements of the job include: • Hands-on experience with digital slide scanners (e.g., Leica, Hamamatsu, Aperio), including basic imaging calibration and maintenance., • Experience working with digital pathology or lab information systems (LIS/LIMS)., • Strong attention to detail with the ability to follow and optimize standardized protocols., • Effective communication and collaboration skills across technical and non-technical teams. It would be a plus if you also possess: • Associate’s or Bachelor’s degree in Histotechnology, Biology, Medical Laboratory Science, or a related field., • 1–3 years of experience working in a histology or pathology laboratory., • Knowledge of histological processes including sectioning, staining, and slide preparation., • Prior experience with digital annotation platforms (e.g., QuPath, or internal tools)., • Experience working in a regulated environment with exposure to CAP/CLIA or IVD workflows., • Understanding of how slide quality and annotation accuracy impact machine learning performance., • Experience in digital pathology workflows and image quality control for AI/ML or research applications.

Digital Pathology Technician Onsite, Vista CA 92081 W2 Contract to Possible Hire The Digital Pathology Technician – AI/ML Support is a key technical role supporting our mission to advance cancer diagnostics through innovative digital pathology solutions. This role combines expertise in digital imaging, histological slide handling and close collaboration across laboratory, engineering, and data science teams. In this role, you will help ensure the accuracy, consistency, and quality of scanned slides used in digital workflows and data-driven applications. You’ll support continuous improvement in slide preparation, scanning, and artifact handling processes, helping enable scalable, high-quality datasets. This position reports to the Manager, SW Developer and is based on-site. In this role, you will have the opportunity to: • Procure, order, organize, and track tissue blocks and histology slides to support digital scanning workflows., • Prepare and load slides for whole slide imaging, ensuring high-quality scans through proper calibration and scanner maintenance., • Perform quality control (QC) on scanned slides, identifying and annotating scan-related or histological artifacts according to defined protocols., • Collaborate with pathologists and lab staff to define, refine, and continuously improve artifact classification and annotation workflows., • Partner with cross-functional teams, including Machine Learning (ML) and Data Science, to align on image quality standards, annotation guidelines, and model training requirements., • Contribute to best practices for digital pathology operations and cross-functional workflows between lab and data science teams. The essential requirements of the job include: • Hands-on experience with digital slide scanners (e.g., Leica, Hamamatsu, Aperio), including basic imaging calibration and maintenance., • Experience working with digital pathology or lab information systems (LIS/LIMS)., • Strong attention to detail with the ability to follow and optimize standardized protocols., • Effective communication and collaboration skills across technical and non-technical teams. It would be a plus if you also possess: • Associate’s or Bachelor’s degree in Histotechnology, Biology, Medical Laboratory Science, or a related field., • 1–3 years of experience working in a histology or pathology laboratory., • Knowledge of histological processes including sectioning, staining, and slide preparation., • Prior experience with digital annotation platforms (e.g., QuPath, or internal tools)., • Experience working in a regulated environment with exposure to CAP/CLIA or IVD workflows., • Understanding of how slide quality and annotation accuracy impact machine learning performance., • Experience in digital pathology workflows and image quality control for AI/ML or research applications.

Other related fields include, but are not limited to: Microbiology, Cell Biology, Genetics, Physiology, Biochemistry, Molecular Biology, Biotechnology, Environmental Science. Benefits: * This is a full-time or part-time REMOTE position * You'll be able to choose which projects you want to work on *

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