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Senior Andrologist (California CLS Required) – Fertility Clinic Job Summary The Senior Andrologist is responsible for performing and overseeing advanced andrology and reproductive laboratory procedures within a fertility clinic setting. This role supports male fertility evaluation, endocrine testing, and assisted reproductive technologies (ART) by performing semen analyses, sperm preparation, and hormone testing while ensuring compliance with California laboratory regulations. The Senior Andrologist also supervises andrology laboratory operations, maintains quality control standards, and collaborates closely with reproductive endocrinologists, embryologists, and clinical staff to support patient care. Key Responsibilities Andrology Laboratory Testing • Perform diagnostic semen analysis according to WHO guidelines and laboratory protocols., • Conduct advanced sperm function testing including:, • Morphology assessment, • Motility and vitality analysis, • Sperm concentration and total motile count, • DNA fragmentation testing when applicable, • Prepare sperm samples for assisted reproductive technologies (ART) including:, • Intrauterine Insemination (IUI), • In Vitro Fertilization (IVF), • Intracytoplasmic Sperm Injection (ICSI), • Process surgical sperm retrieval samples including TESA, PESA, and micro-TESE. Endocrinology & Hormone Testing • Perform and oversee reproductive endocrinology testing related to fertility diagnostics., • Operate immunoassay analyzers including Roche Cobas e411 for hormone testing (e.g., FSH, LH, Estradiol, Progesterone, AMH, Testosterone, hCG, Prolactin)., • Perform linearity verification and calibration verification (CALVER) as required by laboratory validation protocols., • Conduct and document CAP Proficiency Testing (PT) in compliance with CLIA and CDPH regulations., • Troubleshoot analyzer performance issues and perform corrective actions as needed., • Perform routine and scheduled instrument maintenance, calibration checks, and functional verification of the analyzer., • Monitor assay performance and maintain quality documentation for regulatory inspections. Sperm Banking & Cryopreservation • Perform sperm cryopreservation and thawing procedures for fertility preservation and donor banking., • Maintain specimen tracking and chain-of-custody documentation., • Ensure compliance with CAP, CLIA, FDA tissue regulations, and California Department of Public Health (CDPH) requirements. Laboratory Operations & Quality Management • Maintain compliance with California Clinical Laboratory licensing regulations., • Implement and maintain laboratory quality assurance and quality control programs., • Perform method validation, verification, and instrument performance checks., • Assist with preparation for CAP, CLIA, and CDPH laboratory inspections., • Maintain laboratory documentation, standard operating procedures (SOPs), and regulatory records. Leadership & Training • Supervise and train andrology and laboratory technologists., • Ensure staff competency and continuing education compliance., • Assist in development and updates of laboratory SOPs., • Participate in laboratory audits and regulatory readiness activities. Clinical Collaboration • Work closely with reproductive endocrinologists, urologists, embryologists, and nursing staff., • Provide consultation regarding male fertility testing, sperm preparation methods, and endocrine laboratory results., • Participate in multidisciplinary patient case discussions and treatment planning. Required Qualifications Education • Bachelor’s degree or higher in Clinical Laboratory Science, Biology, Biochemistry, or related field. Licensure • Active California Clinical Laboratory Scientist (CLS) License issued by the California Department of Public Health (CDPH). Experience • 5+ years of laboratory experience, preferably in fertility, andrology, or reproductive medicine laboratories., • Experience performing semen analysis, sperm preparation for ART, and hormone immunoassay testing., • Experience operating and troubleshooting Roche Cobas e411 or similar immunoassay analyzers. Preferred Qualifications • Experience working in IVF or assisted reproductive technology laboratories., • Familiarity with CAP accreditation standards, CLIA requirements, and CDPH regulations., • Experience with instrument validation, proficiency testing programs, and regulatory inspections. Key Skills • Advanced knowledge of male fertility diagnostics and semen analysis techniques, • Expertise in ART sperm preparation methods, • Strong knowledge of endocrinology testing and immunoassay instrumentation, • Ability to troubleshoot laboratory instruments and perform technical maintenance, • Thorough understanding of CAP, CLIA, and CDPH regulatory compliance, • Strong attention to detail and laboratory documentation practices, • Effective leadership and communication skills Work Environment • Fertility clinic laboratory setting, • Handling of human reproductive specimens and biological materials, • May require early morning, weekend, or on-call work depending on clinical schedules

About Us Deciphr Health is a seed-stage biotech developing programmable DNA nanostructures for next-generation point-of-care diagnostics. Our first clinical application targets preeclampsia screening — a condition that affects 1 in 25 pregnancies with no adequate rapid test. We're building from our R&D lab in San Carlos, CA. The Role You'll own the aptamer discovery pipeline end-to-end: from SELEX campaign design through NGS-based candidate selection to biochemical characterization of lead binders. This is a hands-on bench role with high autonomy — you'll be the team's go-to expert on nucleic acid selection, modification, and bioconjugation. You'll also contribute to our broader DNA nanostructure platform (with internal training provided). What You'll Do • Design and run SELEX campaigns (affinity-based and capture-release formats) against clinically relevant protein targets, • Perform site-specific bioconjugation of oligonucleotides to proteins, fluorophores, and surface chemistries, • Purify and QC modified oligos and conjugates (HPLC, FPLC, spin-column), • Prepare and manage NGS libraries to identify top aptamer candidates from selection rounds, • Monitor selections via qPCR/RT-PCR and develop binding validation assays, • Support fabrication and testing of DNA nanodevices following internal protocols What We're Looking For • PhD in Biochemistry, Molecular Biology, Chemistry, or related field — or MS with 3–5+ years of hands-on industry experience, • Deep, demonstrated expertise in SELEX (not just familiarity — you've run campaigns), • Strong oligo handling skills: purification, chemical modification, conjugation chemistry, • Proficiency with HPLC, qPCR, and NGS library prep workflows, • Comfort working in a startup environment with minimal infrastructure and high ownership Nice to Have • Exposure to DNA nanotechnology or structural DNA assembly, • Experience with phage display, cell-SELEX, or tissue-based selections, • HPLC instrument maintenance and troubleshooting Compensation Base salary commensurate with experience + meaningful early-stage equity. Location San Carlos, CA (on-site; this is a lab-based role).

Job Title: Associate Scientist Location: South San Francisco CA – 100% Onsite Duration: 12 Months with possible extension Terms: Contract W2 Description: Fully onsite USSF Support biomarker discovery using human samples (whole blood, PBMCs), focusing on generating high-quality, reproducible data in a highly collaborative environment. Responsibilities Execute and analyze experiments with minimal supervision Work with human samples (PBMCs, whole blood) using established protocols Generate, document, and interpret data Optimize assays and troubleshoot experiments Operate key lab platforms and ensure data quality Communicate results and collaborate across teams Qualifications BS in Biology, Immunology, Biochemistry, or related field + 2 years experience Strong hands-on lab skills and experience with human samples Ability to work independently and collaboratively Technical Skills Flow cytometry, Luminex, ELISA Cell culture (primary immune cells preferred) RNA extraction, qPCR Basic data analysis Top 3 Must Have Skill Sets: Strong lab execution and attention to detail Troubleshooting and problem-solving Team-oriented, collaborative mindset

Job DescriptionMyoventive Inc. is a stealth biotechnology company developing precision therapeutics for the treatment of cardiovascular disease. We are seeking a highly motivated and detail-oriented Research Associate to join our biology group. The ideal candidate will support routine molecular biology tasks to advance our research projects. The candidate may have the opportunity to contribute to or learn additional skills such as cell-based assays, protein-based assays and other research tools. This is an exciting opportunity to work in an early-stage company in a highly innovative research environment. Essential Duties and Responsibilities: • Perform molecular assays, including DNA/RNA purification, DNA electrophoresis, RT-PCR, QPCR, ddPCR., • Maintain and culture mammalian cells under aseptic conditions., • Participate in routine tasks (eg. Buffer preparation, assay preparation) as well as research-driven projects (eg. New assay development)., • Assist in troubleshooting and optimization of experimental protocols., • Accurately record experimental data in electronic lab notebooks (ELN) and contribute to data analysis, reporting and presentation., • Work independently on projects as well as collaborate and communicate effectively across teams to ensure project timelines are met., • Support lab maintenance tasks and coordinate the ordering and stocking of laboratory supplies., • Ensure compliance with laboratory safety procedures. Requirements: · Bachelor’s degree in molecular biology, cell biology, biochemistry, biophysics, or related field.· At least 2 years of hands-on laboratory experience in an academic or biotech/industry setting.· Proficiency in key laboratory techniques, including:o DNA/RNA purificationo RT-PCR, qPCR, gel electrophoresis· Strong analytical, quantitative skills, troubleshooting and problem-solving abilities.· Proven ability to work independently and collaboratively within a team.· Strong written and verbal communication skills.· High attention to detail and demonstrated ability to balance routine laboratory tasks with research and development responsibilities. Preferred Qualifications: · Familiarity with antibody therapeutics, SDS-PAGE, Western Blot, ELISA, or other immunoassays. Working Conditions: • May require working in close proximity to blood-borne pathogens., • May require work in an environment where animals are used for teaching and research.

Job Description Bioinformatics Scientist (Mid/Senior) Compensation: $170,000 - $190,000 Location: South San Francisco, CA Job Type: Full-time (Hybrid) Equity: Highly Competitive Equity About Our Client TechStaffers has partnered with one of our clients & they are on a mission to accelerate new cures and promote a healthier planet by unlocking a new level of productivity for scientists. Their sequencing services are used daily by thousands of innovators, including Nobel laureates, Fortune 100 pharma, and over 70,000 scientists. They began by revolutionizing plasmid sequencing, making it exponentially cheaper and faster. Now, they are expanding that same disruptive model across all of genomics, including a new RNA-seq service, to provide scientists everywhere with faster and more affordable access to data. Every team member plays a crucial role in driving the future of biotech research, building the world's most efficient sequencing engine that operates overnight and scales globally. Position Overview We are seeking a highly motivated mid- to senior-level Bioinformatics Scientist to work on the bioinformatics engine that powers this impact. This role is heavily bioinformatics-focused, emphasizing deep domain expertise and the building of scalable products over general software platform skills. You will wear many hats, leading projects from concept through production while maintaining strong ownership of your work. Key Responsibilities • Build blazing-fast, production-grade bioinformatics workflows that process thousands of samples per day., • Develop novel algorithms that turn raw sequencing data into fast, intuitive, and accurate insights., • Hunt down bugs and tame the chaos of real-world sequencing data, including biological artifacts and platform quirks., • Translate bioinformatics outputs into a dynamic scientific UX that feels magical to researchers., • Stay on top of cutting-edge tools and find creative ways to integrate them into real-world pipelines., • Mentor teammates and grow your own skills in a fast-moving, collaborative environment. Qualifications & Requirements • Education: PhD in Bioinformatics, Computer Science, Statistics, Biology, Biochemistry, Physics, or a closely related field., • Experience: 3+ years of experience developing production bioinformatics pipelines., • Industry Background: Minimum of 2 years of industry experience; candidates whose only experience is in academia will not be considered., • Domain Expertise: Strong background in microbial ecology or related fields, with a distinct preference for expertise in microbial genomics., • Technical Tools: Significant, hands-on experience with Nextflow and Docker is critical for pipeline development. Proficiency with standard bioinformatics tooling (Python, Linux, Git) is required., • Sequencing Data: Hands-on work with Illumina or Oxford Nanopore sequencing platforms., • Product Impact: Proven experience building scalable bioinformatics products and clear evidence of delivering impactful, independent projects., • Bonus: Contribution of a novel bioinformatics tool or algorithm is highly regarded as a signal of a top-tier candidate. Ideal Candidate Profile • Thrives with high agency and high ownership, leading projects from idea to production., • Exhibits strong leadership qualities, initiative, and a clear motivation to advance their career., • Is curious about the intersection of biology, algorithms, and software engineering., • Gets excited knowing their work directly accelerates the next generation of medicines and biotechnology., • Values clear communication and loves helping others level up., • Is energized by a tight-knit, fast-paced team environment. Visa Requirements • Visa sponsorship is generally not available., • Able to accommodate TN or H-1B1

Job Description Direct Counsel is partnering with a distinguished American international law firm to find a midlevel associate with 1–5 years of patent prosecution experience in biotechnology. The ideal candidate will have an advanced degree—preferably a Ph.D.—in a life sciences field such as molecular biology, immunology, biochemistry, or cell biology. This position involves working closely with emerging companies on patent prosecution and strategic IP counseling, particularly in cutting-edge areas like antibodies, DNA/RNA therapeutics, chemical biology, and gene-editing technologies. Qualifications: 1–5 years of biotech patent prosecution experience Advanced degree (Ph.D. preferred) in a life sciences discipline USPTO Registration Number (Patent Bar membership) is required Candidates must pass the patent bar exam either prior to joining or within the first 12 months of employment

Job DescriptionBusiness Development Representative - AI Co-Scientist PlatformPerfect for New Graduates with Biology or Related Science Backgrounds About Mithrl We're accelerating the pace of scientific discovery. Our vision: novel drugs and therapies reaching patients in months, not years. Mithrl has built the world's first commercially available AI Co-Scientist—a discovery engine that transforms messy biological data into actionable insights in minutes. Scientists ask questions in natural language and receive real analysis, novel targets, and patent-ready reports. No coding required. No bioinformatics bottlenecks. Our traction speaks for itself: 12X year-over-year revenue growth Trusted by leading biotechs and big pharma across three continents Driving real breakthroughs from target discovery to patient outcomes Why This Role is Perfect for New Science Graduates This is your chance to bridge the gap between cutting-edge science and real-world impact. You'll use your scientific background to communicate with leading researchers while building essential business skills that will accelerate your career. Our BDRs are experiencing some of the fastest pipeline growth and deal velocity in biotech. As a new graduate, you'll get unparalleled exposure to how biotech companies operate, from early-stage startups to Big Pharma R&D teams. You'll initiate conversations with the same caliber of scientists you've studied under, uncovering critical pain points in drug discovery and opening doors to breakthroughs that could lead to life-saving therapies. What You'll Do Core Responsibilities: Research and identify high-potential biotech and pharma companies (Series A+ biotechs, mid-cap pharma, academic research institutions) Craft compelling outbound campaigns targeting scientists, bioinformaticians, and R&D leaders—using your scientific background to speak their language Qualify inbound leads and schedule meetings for our sales and science teams Collaborate with founders and commercial leadership on messaging optimization and market expansion What We're Looking For Educational Background: Bachelor's degree in Biology, Biochemistry, Molecular Biology, Genetics, Bioinformatics, or related life sciences field Master's degree preferred (MS, PhD candidates welcome) Core Skills & Attributes: Exceptional written and verbal communication skills with ability to translate complex scientific concepts for diverse audiences Strong research abilities and scientific curiosity Comfortable with ambiguity and rapid iteration in a startup environment Active listening skills and ability to identify genuine scientific pain points Mindset: Intellectual curiosity about the intersection of science, technology, and business Persistence and resilience—essential for both scientific research and business development Discipline Wins: Our social currency is consistent hard work. We tackle complex problems that require long-term thinking and daily discipline Desire to make a meaningful impact on drug discovery and patient outcomes What You'll Gain Professional Growth: Transform your scientific knowledge into business acumen Front-row seat to AI transformation in drug discovery Competitive base salary designed for new graduates Performance-based commission structure with significant upside potential Work alongside elite scientists, engineers, and commercial professionals High-autonomy, results-driven culture that values scientific rigor Beautiful SF office with in-person collaboration and mentorship

Job Description Active Care Physical Therapy is a world renowned physical therapy clinic seeking highly motivated, professional, out-going and customer-service oriented individual who enjoys working in a fast-paced environment. MEDICAL BILLING Job Description: · Must have experience and knowledge of medical billing · Orthopedic terminology is a plus · Must have knowledge insurance; HMO, PPO; POS; Workers Comp · Answer incoming billing calls, check voicemails daily and respond accordingly and timely · Verify patient eligibility and benefits · Request/process for authorizations · Post patient and insurance payments · Process patient and insurance payments daily · Weekly patient statements · Request for refunds · Follow up on aging accounts receivable; check status on claims and appeals · Scan daily explanation of benefits to billing drive · Submit secondary claims with primary explanation of benefits · Compile deposits as needed · Analyze reports and problem solve · Assist on other projects and duties as assigned · Competent use of computer systems, software, and 10 key calculators · Ability to work well in a team environment · Consistently provide outstanding customer service while maintaining a positive, enthusiastic and helpful attitude · Must be able to multitask and work high volume · Reliable, punctuality and dependability · Be able to work under minimal supervision · Full time position and must be able to work in the office · Benefits · Health promoting/active setting Company DescriptionLisa Giannone, Active Care founder, has developed and masterminded an approach on treating orthopedic and sports injury that has been highly successful. Her system involves a point of view in analysis, the development of a working theory for each individual patient case, and an understanding of mechanics and the kinetic chain and its influence on the recovery path. In her system, each step of the rehab process must be supported by a "why" that both the patient and therapist understand. This is not cookie-cutter or textbook as Lisa's theories and practices developed out of her academic background in biochemistry, physiology, and biomechanics and through the more than 30 years of experience she has in the field. The vast majority of the techniques and exercises used to manage AC patients were developed and nuanced by Lisa and make up her system of care and training. All practitioners of AC are trained to practice within this system and learn directly from Lisa. She guides her team from her belief that "Exercise is the Medicine", "that it is only through methodical mechanical work to the body both manually and through proprietary exercise series that real and lasting, durable recovery can be accomplished in orthopedic and sports injury." We have been in practice for more than 30 years keeping athletes and athletically ambitious patients moving forward.Lisa Giannone, Active Care founder, has developed and masterminded an approach on treating orthopedic and sports injury that has been highly successful. Her system involves a point of view in analysis, the development of a working theory for each individual patient case, and an understanding of mechanics and the kinetic chain and its influence on the recovery path. In her system, each step of the rehab process must be supported by a "why" that both the patient and therapist understand. This is not cookie-cutter or textbook as Lisa's theories and practices developed out of her academic background in biochemistry, physiology, and biomechanics and through the more than 30 years of experience she has in the field. The vast majority of the techniques and exercises used to manage AC patients were developed and nuanced by Lisa and make up her system of care and training. All practitioners of AC are trained to practice within this system and learn directly from Lisa. She guides her team from her belief that "Exercise is the Medicine", "that it is only through methodical mechanical work to the body both manually and through proprietary exercise series that real and lasting, durable recovery can be accomplished in orthopedic and sports injury." We have been in practice for more than 30 years keeping athletes and athletically ambitious patients moving forward.

Job DescriptionDescription: • Set-up, prepare, and operate upstream manufacturing equipment/labware/assemblies (includes scaleup, bioreactors, harvest filtration including centrifugation, autoclave/sterilizer, bench top analytical instruments (pH/conductivity/osmometer), etc.) in accordance with current good manufacturing practices (cGMP)., • Record and document procedures with detail and accuracy. This includes batch records, training records, logbooks, standard operating procedures (SOPs) and validation protocols., • Execute quality systems (including critical work orders, change controls, deviations, corrective action preventative action (CAPA))., • Create and revise standard operating procedures, batch records, part numbers, specifications, etc., • Weigh and prepare cell culture media, buffers, and solutions., • Coordination and collaboration of activities with other departments, and with vendors., • Sample solutions and perform analytical assays (including cell counts, pH, conductivity, etc.), • Maintain clean room work areas (including floors, benches, bioreactors, chromatography skids, etc.) waste disposal, lean manufacturing and good manufacturing practices (GMP)/compliance.Requirements:, • 2 years of college science in Cell Biology, Biochemistry, Chemistry, Biology, with 2 to 4 years of related experience., • Or 4 to 8 years of experience and/or training, or equivalent combination of education and experience., • Knowledge of downstream equipment (scaleup, bioreactors, harvest filtration, flow/UV/pH/conductivity/etc. sensors), filtration equipment, solution preparation equipment (laminar air flow hood, agitator mixers, bench top instruments) are essential for this position., • Attention to detail and accurate record keeping and documentation is mandatory in this position., • Teamwork and communication are key attributes needed for this position. A collaborative attitude and a positive work ethic are key traits for success., • Work safety is essential for this position.

Job DescriptionCompany Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description About the Team AbbVie Biologics Analytical Research & Development (Biologics ARD) is a global analytical sciences organization responsible for CMC analytical development of AbbVie's pipeline of innovative therapeutic biologic products. We are a world-class team of scientists and leaders united by a shared mission to drive the advancement of industry-leading analytical capabilities and meaningfully contribute to advancing AbbVie’s pipeline of innovative medicines. The Biologics ARD team at the AbbVie Bay Area site in South San Francisco has a long and rich history of biologics development. Located in a state-of-the-art facility housing end-to-end CMC development capabilities, the team works collaboratively to advance novel biologic therapeutics – including multi-specifics, ADCs, antibodies, and novel modalities – into first-in-human clinical development and through to clinical proof of concept. Careers in AbbVie Biologics ARD provide unique opportunities to work with cross-functional and global teams to drive exceptional science and innovative product development strategies. Role Summary The Analytical Lead owns the analytical development strategy and deliverables for assigned biologic programs and serves as the primary analytical point of contact on the CMC development teams for these programs. Deliverables span product control strategies, CQA assessments, characterization and comparability studies, release and stability packages, and regulatory submission content. The Analytical Lead is responsible for coordinating method development, validation, transfer, and clinical supply testing across internal lab teams, Quality Control, and external contract labs. The role operates within a cross-functional, on-site environment supporting a portfolio that includes multi-specifics, antibodies, ADCs, and novel modalities. Responsibilities • Independently conceive and own the analytical development strategy for assigned programs – including methods, specifications, CQAs, stability study plans, extended characterization, and comparability assessments – in alignment with CMC project goals., • Translate program analytical strategy into clear, scoped work packages for internal lab teams., • Accountable for the timely delivery of respective analytical work packages to achieve agreed upon CMC development objectives., • Manage and oversee third-party laboratory work to ensure quality and on-time execution., • Interpret data trends across release, stability, and characterization assays., • Collaborate with process development and drug product development partners to define analytical strategies for process development and formulation development studies., • Author and review regulatory submission documents, responses to health authority queries, technical reports, lab data, and method validation protocols and reports., • Communicate strategy, risks, and key issues to the Product Development Strategy Team, functional management, and SMEs., • Present project updates at group, department, and project team meetings., • Plan resource and budgetary requirements for assigned programs., • Mentor dual-role analytical leads on project management and analytical development strategies., • Serve as a subject matter expert within the broader Biologics ARD team for processes and procedures relevant to the Analytical Lead role., • Compile program-level analytical information into consolidated reporting for Analytical management.Qualifications, • Degree in Chemistry, Biochemistry, Analytical Chemistry, or a related field. PhD with 8+ years, MS with 14+ years, or BS with 16+ years of relevant industry experience., • Comprehensive knowledge of analytical methods for release, stability, and extended characterization of protein therapeutics (HPLC, capillary electrophoresis, mass spectrometry, potency assays, ELISA, cell-based functional assays, CD, DSC, light scattering)., • Proven track record in project management of analytical development activities for biologic compounds (multi-specifics, mAbs, antibody drug conjugates and/or fusion proteins)., • Experience authoring and reviewing INDs/IMPDs, including quality and characterization sections, and authoring responses to health authority queries., • Experience leading and reviewing change records, exception reports, and laboratory investigations in a GXP environment., • Working knowledge of global regulatory requirements applicable to analytical development of protein therapeutics (ICH, FDA, EMA)., • Statistical knowledge and hands-on experience with design of experiments, stability trending, statistical software packages (e.g. JMP)., • This position requires an individual who is self-motivated, detail-oriented, and able to work in a fast-paced team environment with demonstrated problem solving skills. Key Competencies • Strong technical, communication, collaboration, and critical thinking skills., • Must be adaptable and flexible in the face of evolving priorities and timelines., • Fosters a learning environment, open to suggestions and experimentation for improvement., • Embraces the ideas of others, nurtures and manages innovation to reality. Work Environment This is a full-time, on-site role located in South San Francisco, CA. The position requires daily in-person collaboration across scientific and cross-functional teams. Candidates should expect frequent interaction with both local and global colleagues. Compensation & Leveling Compensation and Leveling will be commensurate with experience. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees. This job is eligible to participate in our long-term incentive programs. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job DescriptionDescription: • Set-up, prepare, and operate upstream manufacturing equipment/labware/assemblies (includes scaleup, bioreactors, harvest filtration including centrifugation, autoclave/sterilizer, bench top analytical instruments (pH/conductivity/osmometer), etc.) in accordance with current good manufacturing practices (cGMP)., • Record and document procedures with detail and accuracy. This includes batch records, training records, logbooks, standard operating procedures (SOPs) and validation protocols., • Execute quality systems (including critical work orders, change controls, deviations, corrective action preventative action (CAPA))., • Create and revise standard operating procedures, batch records, part numbers, specifications, etc., • Weigh and prepare cell culture media, buffers, and solutions., • Coordination and collaboration of activities with other departments, and with vendors., • Sample solutions and perform analytical assays (including cell counts, pH, conductivity, etc.), • Maintain clean room work areas (including floors, benches, bioreactors, chromatography skids, etc.) waste disposal, lean manufacturing and good manufacturing practices (GMP)/compliance.Requirements:, • 2 years of college science in Cell Biology, Biochemistry, Chemistry, Biology, with 2 to 4 years of related experience., • Or 4 to 8 years of experience and/or training, or equivalent combination of education and experience., • Knowledge of downstream equipment (scaleup, bioreactors, harvest filtration, flow/UV/pH/conductivity/etc. sensors), filtration equipment, solution preparation equipment (laminar air flow hood, agitator mixers, bench top instruments) are essential for this position., • Attention to detail and accurate record keeping and documentation is mandatory in this position., • Teamwork and communication are key attributes needed for this position. A collaborative attitude and a positive work ethic are key traits for success., • Work safety is essential for this position.

Job DescriptionDescription: Manufacturing Operations · Execute and monitor aseptic fill/finish activities including pooling/mixing, filtration, vial/syringe filling, capping, visual inspection, labeling, and packaging in full compliance with cGMP. · Operate, monitor, and troubleshoot automated and semi-automated filling, inspection, labeling, packaging and serialization equipment. · Perform sterile gowning and work effectively in Grade A/B/C/D cleanroom environments. · Conduct in-process sampling, support environmental monitoring, and perform real-time quality checks. · Execute in-process checks, environmental and system monitoring, and alarm/exception response according to validated procedures. · Troubleshoot system faults and escalate mechanical, software, or sterility-related issues when required. · Perform manual and semi-automated visual inspection of sterile drug products to detect particulates, cosmetic defects, and container-closure abnormalities. · Maintain visual inspection proficiency by completing required annual operator qualification assessments. · Undergo and maintain compliance with the annual eye examination requirement to ensure visual acuity necessary for inspection tasks. · Support upkeep of defect libraries, inspector training files, and trending of reject categories. · Escalate atypical findings and actively contribute to root cause investigations for inspection-related deviations. · Set-up, prepare, and operate manufacturing equipment/assemblies (includes freeze/thaw equipment, filtration assemblies, drug product fill equipment, filter integrity tester, environmental monitoring system, visual inspection booth, labeling machine, packaging machine) in accordance with current good manufacturing practices (cGMP). · Perform clinical and commercial labeling, packaging, and serialization activities in accordance with the manufacturing order. Equipment, Facilities, and Readiness · Perform equipment changeover, cleaning, sanitization, and routine maintenance. · Support basic equipment troubleshooting and coordinate with internal teams or vendors as needed. · Maintain cleanroom readiness, including room sanitization and equipment status verification. · Set up, operate, and maintain manufacturing equipment (e.g., freeze/thaw systems, filtration assemblies, filling equipment, filter integrity testers, visual inspection booths). Process & Documentation · Support development and refinement of Fill/Finish processes and Bills of Materials. · Participate in tech transfer, engineering runs, qualification, and validation activities. · Accurately complete batch records, logbooks, and electronic documentation in compliance with GDP. · Create and revise SOPs, batch records, specifications, bill of materials, and other GMP documents. Quality Systems & Continuous Improvement · Participate in deviations, CAPAs, root cause investigations, change controls, and other quality system activities. · Identify process and equipment improvement opportunities; contribute to LEAN, 5S, and Six Sigma initiatives. · Provide hands-on and classroom training to team members. Safety · Follow all safety procedures, including proper handling of biologics, cleaning agents, and raw materials. · Escalate safety concerns and support safety audits and required training. Requirements: QUALIFICATIONS – SKILLS & REQUIREMENTS: · Background in Biological or Chemical Sciences. · Proficiency with Microsoft Office; experience with SAP or similar ERP is a plus · Comprehensive understanding of aseptic techniques, media fill qualifications, and contamination control strategies. · Basic proficiency in equipment control and automation processes · Strong organizational and record-keeping skills. · Ability to work independently, collaborate within teams, or lead assigned tasks. · Effective verbal and written communication skills. · Ability to lift = 50 lbs, work in hot/cold or wet environments, and perform repetitive motions. · Color differentiation and clear visual acuity required for inspection tasks. · Ability to work with and around large equipment · Ability to lead small operational teams or initiatives. · Knowledge of cGMP’s. EDUCATION & EXPERIENCE: · Associate-level coursework (2 years science-focused) in Cell Biology, Biochemistry, Chemistry, or a related field plus 2–4 years of relevant experience, OR · 4–8 years of directly related industry experience and/or training, or equivalent combination of education and experience WORK ENVIRONMENT: This is a Manufacturing position, located in our manufacturing facility in Emeryville, CA. The physical demands described here are representative of those that must be met by an individual to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the individual is: · Must possess visual acuity adequate to identify small defects under controlled lighting conditions. · Near vision and color perception sufficient to distinguish particulate matter and cosmetic defects in transparent and amber containers. · Ability to maintain sustained visual concentration during repetitive inspection activities. · Corrective lenses are permitted if vision is corrected to satisfactorily perform inspection duties. Moderate noise (i.e., background noise due to computers, phone, printers, and light hallway traffic). · Constantly required to use hands and fingers to operate office machines and equipment. · Frequently required to reach with hands and arms. Occasionally required to stoop, kneel, and crouch. · Able to work a flexible schedule as needed. · Accessibility via Cell Phone · Work a nonstandard schedule. · Work evening or night shift hours. · Provide coverage for other positions, shifts, or functions. · Frequently required to sit and/or stand, walk, talk, and hear. · Ability to sit at a computer for an extended period of time

Job Description About Allogene: Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T™) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients. About the role: Allogene is seeking a highly motivated Senior Associate Scientist to support the development and characterization of clinical-scale manufacturing processes for Allogene’s CART therapies. This individual will contribute to the development, implementation and characterization of state-of-the-art processing technologies to deliver scalable and robust manufacturing processes, and support successful tech transfer for GMP manufacturing and release. This position will also contribute to the development of novel technologies and approaches to meet future CART manufacturing needs. Responsibilities: • Actively contribute to development, implementation, characterization and successful execution of robust, state-of-the-art CART manufacturing processes., • Execute and analyze Design of Experiments (DoE) studies to support process understanding, optimization, and characterization activities., • Support clinical‑scale non‑GMP manufacturing operations for execution of BLA‑enabling process characterization activities., • Support and contribute to process characterization efforts and continuous improvement initiatives aimed at enhancing CAR‑T manufacturing processes and capabilities (e.g., evaluation of process parameters, materials, closed or disposable systems, and operational workflows)., • Contribute to Project Technical Teams and communicate and collaborate effectively to ensure effective interactions with all stakeholder groups., • Ensure high-quality, timely documentation in electronic laboratory notebooks and Technical Reports and contribute to Regulatory Filings and responses to Regulatory questions as appropriate., • Present data/strategy to scientists (and management) in internal venues (technical meetings, Project Team meetings) as appropriate., • Remain current with relevant cell therapy, immunology, and bioprocessing literature., • Other duties as assigned Requirements: • BS in Chemical Engineering, Biochemistry, Molecular & Cell Biology, or Immunology or related degree, • MS plus at least 2 years experience or BS with at least 5 years experience, • A demonstrated foundational understanding of mammalian or primary cell culture, biochemistry, molecular & cell biology and immunology (required for enhanced product & process understanding)., • Experience with prior Gene & Cell Therapy manufacturing preferred, but not required., • Experience with continuous manufacturing processes including operation in upstream genetic modification and bioreactor/WAVE expansion, and cryopreservation preferred., • Experience in genetic modification of cells using gene edit and gene delivery technologies preferred, but not required., • Experience in flow cytometry for T cells characterization preferred, but not required., • Experience in FMEA, process characterization and DOE methodologies in biologics or cell therapy space preferred., • Ability to work in a fast-paced, startup environment., • Strong attention to detail with the ability to multi-task and handle multiple responsibilities simultaneously., • Excellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelines., • Ability to work independently and as part of a team., • Strong interpersonal skills including verbal and written communication are essential in this collaborative work environment., • Candidates must be authorized to work in the U.S., • This is a 1-year contract opportunity with the possibility of extension or contract-to-hire. We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more. The expected hourly range for this role is $45 to $50 per hour. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law. As an equal opportunity employer, Allogene is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients. #LI-Onsite #LI-TF1

Job DescriptionPilot Plant Technician, Food Science and Product Development, Full-time, ExemptSouth San Francisco, CA Alpine Bio is a plant ingredient and genetics company focused on redefining protein production from the soil up. We believe that replacing resource-intensive protein production methods based on animal agriculture with highly efficient and regenerative systems can facilitate rapid, planet-scale changes. Our proprietary biomanufacturing platform makes this possible. Since 2016, we’ve been transforming soybeans into the world’s most efficient protein factories, harnessing their natural ability to create functional proteins at scale and unprecedented efficiency. Using our expertise in purifying proteins we created the world's most soluble and neutral tasting plant proteins, and invite you to be a part of the revolution in plant-based ingredients! About the Role: We are looking for a Pilot Plant Technician to become part of primary operations in our Pilot Plant. Your main focus will be to purify plant proteins at pilot-scale, primarily from soybeans and soy-based ingredients. The job entails batching of ingredients (including food allergens), preparing solutions, operating pilot scale equipment and performing post-process shut-down and cleaning procedures. Ability to perform all operational tasks safely and according to relevant operating procedures is essential. Who you are: • Operator with at least basic familiarity with food and protein processing equipment;, • Committed to Pilot Plant operations excellence and quality., • Safety-minded, proactively spotting potentially unsafe situations and prioritizing safety., • Perceptive, able to spot variations from expected conditions and results., • Adaptable, quick learner hands-on problem solver., • Team player who thrives at communicating and collaborating with colleagues, • Passionate about our mission of creating animal-free foods for the 99% of people who are unwilling to compromise on taste and price Responsibilities:, • Purify plant proteins at pilot scale (10-500L), ensuring that they meet target quality requirements using equipment such as tanks, decanters, centrifuges, filtration units, pasteurizers, and dryers, • Follow, fill out and, over time, help to develop detailed documentation such as batch records., • Operate, clean, and maintain pilot equipment and facility according to SOPs., • Monitor equipment and instruments, including flow meters, pumps, and control valves., • Prepare processing buffers and solutions., • Help manage pilot plant consumables and raw materials inventory.Required Skills and Experience:, • Associate’s or Bachelor’s degree in a life science or engineering discipline (biology, biochemistry, molecular biology, biotechnology, chemical engineering, or similar)., • Some experience in a manufacturing, pilot, or R&D lab environment (>1 year preferred)., • Ability to lift and carry up to 50 pounds and/or position the body to reach items on the floor/below knee level or reach overhead., • Excellent organizational, communication, and interpersonal skills., • Resourceful, eager to learn, and team-oriented, with meticulous attention to detail., • Ability to work independently in a timely manner., • Please note that this role involves working with soy and soy-derived materials.Closing: The pay range is currently between $75,000 to $85,000 in annual gross compensation. Within the range, individual pay is determined by many factors, including job-related skills, experience, and relevant education or training. Alpine Bio offers competitive compensation, generous healthcare, dental and vision plans, and 401(k).

Job Description About Allogene: Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T™) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients. For more information, please visit www.allogene.com, and follow @AllogeneTx on X (formerly Twitter) and LinkedIn. About the role: Allogene Therapeutics is seeking Senior Director, Head of Process Sciences group within the Process and Product Development organization. This role will be responsible for driving innovation, developing new cell therapy technologies, and implementing robust CAR-T processes to advance Allogene’s core technologies in our GMP manufacturing facilities. This individual will be responsible for leading Drug Substance and Drug Product teams developing early and late-stage CAR-T processes across Allogene’s pipeline. This role is onsite in our HQ in South San Francisco, CA and reports directly to the Executive Director, Process and Product Development. We encourage applicants who believe they have the skills and drive to succeed at Allogene to apply for this role. Responsibilities include, but are not limited to: • Lead Cell Starting Material, Drug Substance, and Drug Product process development teams responsible for early and late-stage manufacturing processes, • Build strong relationships and collaborate effectively to ensure seamless interactions with internal and external partners and stakeholders; Lead and contribute to Project Technical Teams as appropriate, • Apply Quality by Design principles to develop a deep understanding of process-to-product relationships to define and enable robust, integrated BLA enabling control strategies, • Lead the development of robust risk assessments that set the foundation for platform process knowledge and process/raw material characterization. Responsible for process development and process characterization plans utilizing Design of Experiments and Quality by Design methodologies, • Ensure high-quality across teams, timely documentation in electronic laboratory notebooks and Technical Reports, • Contribute to Regulatory Filing strategy and content, and responses to Regulatory questions as appropriate (IND through BLA), • Demonstrate strong leadership, personal accountability and interpersonal skills, and capability for mentoring junior and senior colleagues (direct reports, their direct reports and others), and establish safe, high-quality lab practices, • Maintain awareness of current state of the field (literature, Regulatory expectations and competitive surveillance) and collaborate on/ author external publications and present at external conferences as appropriate, • Other duties as assigned Position Requirements & Experience: • PhD, MS or BS in Chemical Engineering, Biochemistry, Molecular & Cell Biology, Immunology or the related field with 12+ years of relevant experience required with at least 5 years in a management role leading a team, • A demonstrated foundational understanding of mammalian or primary cell culture, biochemistry, molecular & cell biology and immunology (required for enhanced product & process understanding), • Experience with development and manufacture of viral vectors and gene editing technologies desired, • Proven ability to successfully manage multiple process development functions in complex biological processes is expected, including significant experience with process characterization/ validation/ commercialization; Cell and gene therapy experience a plus, • Demonstrated technical and strategic leadership and problem-solving skills, • Experience in cell therapy manufacturing processes and technology transfer, • Ability to work in a fast-paced, dynamic, startup environment, • Strong attention to detail with the ability to multi-task and handle multiple responsibilities simultaneously, • Experienced leader of scientific teams, • Experienced project management/leadership skills, • Strong interpersonal skills with the ability to establish, motivate and lead highly-functioning teams, and influence across organizational boundaries, • Excellent organizational skills and an ability to prioritize effectively to deliver results within reasonably established timelines, • Ability to work independently and as part of a team, • Candidates must be authorized to work in the U.S. We offer a chance to work with talented people in a collaborative environment and provide a top-notch compensation and benefits package, which includes an annual performance bonus, equity, health insurance, generous time off (including 2 annual holiday company-wide shutdowns) and much more. The expected salary range for this role is $230,000 to $270,000. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law. As an equal opportunity employer, Allogene is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state and local laws. We also embrace differences in experience and background, and welcome diversity of opinions and thought with active recruitment and internships designed to create a stronger and better Allogene that is focused on developing life-changing products for patients. #LI-TF1 #LI-Onsite

Job DescriptionAbout Us Becoming is building a Developmental Intelligence™ platform that combines biology, engineering, and AI to understand, model, and guide development. We design and operate integrated biological and technological systems that enable new approaches to tissue generation, regenerative medicine, and therapeutic discovery. Our team brings together expertise across developmental biology, tissue engineering, hardware, software, and operations. We are mission-driven, highly collaborative, and focused on building foundational capabilities that can scale from early research through clinical and translational applications. Position Overview We are seeking a highly capable Lab , Research & Operations Manager to join our growing team in San Francisco. This is a manager-level, hands-on role that combines in vivo research execution with ownership of laboratory operations, safety, compliance, and operational excellence. This role is a steward of lab health and safety and a central operational leader. You will establish and maintain SOPs, ensure inspection-ready lab and vivarium operations, manage projects across teams, and track KPIs that keep the organization running safely, efficiently, and on schedule. The ideal candidate thrives in an early-stage environment, enjoys both bench work and systems-building, and takes pride in creating order, safety, and repeatability in complex scientific operations. Key ResponsibilitiesLab, Vivarium & Safety Operations • Own day-to-day laboratory and vivarium operations, ensuring a safe, clean, compliant, and inspection-ready environment at all times, • Serve as a primary steward of lab health and safety, including biosafety, chemical hygiene, animal welfare, waste management, and equipment safety, • Establish, document, implement, and continuously improve Standard Operating Procedures (SOPs) covering lab operations, vivarium workflows, animal handling, biosafety, equipment use, and waste disposal, • Ensure SOPs are version-controlled, actively followed, trained on, and audited, not just written, • Lead onboarding and recurring training for staff on SOPs, lab safety, and compliance requirements, • Support and coordinate IACUC, EH&S, and internal audits, inspections, and protocol updates, • Coordinate equipment maintenance, calibration schedules, certifications, and vendor service visits, • Manage animal deliveries, cage cleaning coordination, and accurate animal care documentation, • Handle, breed, and maintain animal colonies and perform tissue collection as required Research & Histology Support, • Perform mouse embryo dissections and tissue isolations from early developmental stages, • Conduct in vivo procedures including IV, IP, and PO dosing; necropsy; tissue collection; and sample processing in rodent models, • Monitor animal health and maintain accurate experimental records in compliance with ethical and regulatory standards, • Validate and perform in vitro assays to evaluate tissue-engineered constructs, • Perform primary and iPSC cell culture using aseptic techniques, • Prepare samples for flow cytometry, RNA sequencing, and histological staining, • Analyze and interpret histological and experimental data and present findings to cross-functional teams, • Collaborate closely with research, engineering, and manufacturing teams to advance therapeutic programs Operations, Project Management & KPI Tracking, • Own operational project management across lab, vivarium, and biomanufacturing workflows, • Create and maintain lightweight project plans, timelines, and dependencies for research, infrastructure, and operational initiatives, • Define, track, and report key operational KPIs, including but not limited to:, • Lab uptime and equipment availability, • Inventory accuracy and stockout rates, • Safety incidents and corrective actions, • Animal colony health, utilization, and throughput, • Experiment turnaround times, • Build and maintain dashboards or reporting systems (e.g., spreadsheets, Notion, Airtable, or similar) to provide visibility into operational performance, • Identify operational bottlenecks and inefficiencies and drive process improvements through execution, • Partner with leadership and cross-functional teams to align operational execution with company priorities and milestones Purchasing & Inventory Management, • Manage ordering of lab supplies, reagents, consumables, and office materials, • Maintain accurate, real-time inventory systems and optimize stock levels, • Coordinate with vendors and sales representatives on delivery timelines, backorders, and issue resolution, • Ensure safe storage, labeling, and tracking of chemicals, biologicals, and controlled materials Biomanufacturing & Hardware Support, • Operate biomedical-grade resin 3D printers, • Perform post-processing, • Assist with assembly, bonding, tubing, and fittings, • Conduct testing and basic quality control checks, • Sterilize equipment and components in accordance with safety and quality standards Requirements Qualifications • Master’s degree in Biology, Bioengineering, or a related scientific or engineering discipline, • Minimum of 2 years of experience in in vivo research and laboratory operations, • Hands-on experience with animal handling, dosing, pathology, and surgical procedures, • Demonstrated understanding of laboratory safety, biosafety, and animal welfare best practices, • Proven ability to create, maintain, and enforce SOPs in a laboratory or vivarium environment, • Strong organizational skills and exceptional attention to detail, • Clear written and verbal communication skills, • Ability to work independently while collaborating effectively in a fast-paced startup environment Preferred Qualifications • Proficiency in cell culture, molecular biology, and biochemistry techniques, • Experience supporting preclinical or IND-enabling studies, • AALAS certification or equivalent, • Experience with electronic inventory systems or LIMS, • Knowledge of GLP standards, • Prior experience supporting IACUC, EH&S, or regulatory inspections, • Experience managing projects and tracking operational KPIs Benefits • Competitive salary and meaningful equity, • Full benefits, • High-trust, high-ownership environment, • The opportunity to define a new scientific category from the ground up

Job DescriptionDescription: • Assist in the creation of the Bill of Materials for the upstream process., • Assist in development and creation of the upstream process., • Monitor upstream operations (including trouble shooting and diagnosis of instruments, equipment, process, etc.), • Set-up, prepare, and operate manufacturing equipment/labware/assemblies (includes scaleup, bioreactors, harvest filtration including centrifugation, autoclave/sterilizer, bench top meters (pH/conductivity/osmometer), etc.) in accordance with current good manufacturing practices (cGMP)., • Based on business needs there will be some cross training to support upstream operations (includes filtration skid, chromatography skid, viral filtration skid, TFF skid, Bulk fill, Freeze/Thaw, etc.) in accordance with current good manufacturing practices (cGMP)., • Record and document procedures with detail and accuracy. This includes batch records, training records, logbooks, standard operating procedures (SOPs) and validation protocols., • Execute quality systems (including critical work orders, document change requests, change control, deviations, corrective action preventative action (CAPA))., • Create and revise standard operating procedures, batch records, part numbers, specifications, etc., • Weigh and prepare culture media, feeds, buffers, and solutions., • Coordination and collaboration of activities with other departments, and with external vendors., • Sample solutions and perform analytical assays (including cell counts, pH, conductivity, etc.), • Perform technical training for staff (including hands-on and class-based training), • Assist CMC team with technical transfer activities., • Identify and implement equipment and process improvements., • Maintain clean room work areas (including floors, benches, bioreactors, chromatography skids, etc.) waste disposal, lean manufacturing and good manufacturing practices (GMP)/compliance.Requirements:, • 4 years of college science in Cell Biology, Biochemistry, Chemistry, Biology, with 2 to 4 years of related experience., • Or 4 to 8 years of experience and/or training, or equivalent combination of education and experience., • Proficiency of upstream equipment (scaleup, bioreactors, harvest filtration, flow/UV/pH/conductivity/etc. sensors), filtration equipment, solution preparation equipment (laminar air flow hood, agitator mixers, bench top instruments) are essential for this position., • Attention to detail and accurate record keeping and documentation is mandatory in this position., • Teamwork and communication are key attributes needed for this position. A collaborative attitude and a positive work ethic are key traits for success., • Flexible work hours as business requires.

Job DescriptionPosition Summary Cellares is seeking an innovative and highly motivated Senior Scientist with expertise in cell therapy manufacturing to join the Process Development team. This individual will interface across many parts of the company and contribute significantly to the development of our advanced cell therapy manufacturing platform. The primary focus of this position is to design, coordinate, execute and analyze cell therapy process development experiments that expand and drive continuous improvement of the Cellares platform. The ideal candidate will be a highly organized technical leader and cross-functional collaborator with demonstrated expertise in developing robust autologous and allogeneic cell therapy processes. Candidates should also enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.Responsibilities • Design and execute complex experiments using scientific principles and statistical approaches (DOE) to support the development of the Cellares platform, • Interface internally and cross-functionally with Analytical Development, MSAT, Quality, Manufacturing, BD, Product, and Engineering to implement new processes and technologies as part of the core technology transfer team, • Author and review technical documents, procedures and reports to ensure accuracy and quality, • Present technical and programmatic information to internal and client-facing stakeholders, • Coordinate day-to-day team efforts and provide technical training and guidance to junior team members, • Develop training materials for scientific methods and techniques, train and onboard new hires, • Serve as subject matter expert where appropriate for the cell and gene therapy process, provide technical insights and support in troubleshooting and root cause investigationsRequirements, • Bachelor's, Master's, or PhD in Bioengineering, Chemical Engineering, Biology, Biochemistry, or related field with 6-21 years of process development experience in the cell and gene therapy field, • Subject-matter expert in T cell, HSC, or other immune cell therapy modality, • Extensive hands-on experience with commercial cell processing instruments (Miltenyi Prodigy, Lonza Cocoon, Xuri Wave) relevant to cell selection/purification and expansion, • Familiarity with diverse cell editing technologies (LVV, RVV, LNP) and processes (transduction, transfection, electroporation, etc.), • Excellent verbal and written communication skills; able to interpret, summarize, and present scientific results in a clear, concise, accurate manner to both technical and non-technical audiences, • Knowledge and understanding of cGMP regulations and ICH guidelines preferred, • Self-awareness, integrity, authenticity, and a growth mindset.Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.This is Cellares Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing. Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job DescriptionA Bit About Us We are Arcadia Science, an evolutionary biology company founded and led by scientists. Our mission is to turn natural innovations into real-world solutions by developing systematic and quantitative approaches to leveraging biology for therapeutics R&D. We share our research as openly as possible to accelerate discovery and make our work broadly useful. The Opportunity We’re closing the gap between biological data and biological understanding. Our Validation team does this by closing the design–build–test–learn loop through lab validation across diverse organisms. Read more about our work through our publications. We are seeking an Experimental Validation Biologist with a special expertise in cell biology to join our Validation team. In this role, this scientist will generate phenotypic and genotypic data to compare cellular features across organisms. Because we use evolution to select the best organism to study each biological question, scientists in this role should expect to work with diverse, often non-traditional organisms and cell types. These contributions will be instrumental in validating existing tools at Arcadia, testing novel hypotheses, identifying potential therapeutic assets, and driving the creation of novel cellular approaches for testing biological function. Top candidates are hands-on, efficient scientists with deep experience in cell biology and a strong interest in using biological diversity as a tool to unlock novel therapeutics. They are energized by evaluating novel biology, skilled at troubleshooting, and thrive in collaborative and open research environments. Enthusiasm and participation in open science is also required as we routinely share our findings via our open-source pubs. Key Responsibilities: • Develop, adapt, and optimize experimental workflows for gathering high-dimensional phenotypic data across diverse cellular and organismal systems, • Validate platform tools and test predictions using cell-based or organism-based assays, • Identify maximally informative measures for comparing cellular features across organisms, • Conceptualize and prototype novel tools and methodologies to expand Arcadia’s capabilities in cell biology, • Troubleshoot experimental challenges independently and creatively, • Collaborate with cross-disciplinary teams to contribute to shared research goals and accelerate broader scientific efforts, • Keep detailed experimental records and documentation (SOPs) for all workflows, • Synthesize ideas, data, and findings into fully open-access pubs and engage with the scientific community to maximize impact and garner feedback that improves the workQualifications, • Ph.D. or equivalent experience in Cell Biology, Molecular Biology, Biochemistry, or a related field, • At least 3 years of full-time relevant scientific experience post-PhD or relevant experience, • Demonstrated expertise in cell- or organism-based assay development, including independent design, execution, and optimization, • Proficiency with core cell biology tools, with a particular focus on those that can gather large-scale, high-dimensional data (e.g., live cell imaging, spectroscopy, etc.), • Experience with core molecular biology tools and techniques, • Experience independently coordinating and driving multi-stage experimental projects, • Comfort working with diverse cellular organisms and systems, • Familiarity with data analysis using python or R, • Excellent verbal and written science communication skills for both general and technical audiences as we expect all scientists to actively draft and openly publish their results Compensation:Successful applicants can expect to be compensated between $130,000-$180,000 with benefits and a competitive equity offering, depending on experience level. The position will require the individual to be on-site at our Emeryville, California headquarters. Application Process:Interested applicants should apply using the link below.. Arcadia is an equal opportunity workplace; we welcome people from all backgrounds and communities. We provide competitive compensation and practical benefits to keep you happy and healthy so that you can do your best work. Please note that an offer of employment at Arcadia is contingent upon the successful clearance of a reference and background check.

Job Description Position: Biotech Program Manager Location: South San Francisco Type: Full-time Ohalo is hiring a Biotech Program Manager (PM) to lead one or several discovery, development, or production programs. You will manage and oversee programs focused on discovering molecules, or developing transformation or acceleration techniques, working at the molecular, cellular, and whole plant levels. This is a full-accountability leadership role: you will act as the general manager for a set of breakthrough technology programs, owning outcomes, defining strategy, and managing the work of cross-functional individuals from science, engineering, and operations. You will be responsible for setting deliverables, assigning work, developing and updating timelines, and ensuring on-time delivery of outcomes. This role requires a candidate who is competent with molecular or cellular biology or biochemistry (but is not necessarily a plant scientist), has experience designing, developing, and managing high throughput and automated lab workflows, has strong leadership and organizational skills, and is very capable and proven in leveraging AI tools to accelerate and scale work output. The ideal person thrives in a high-ownership, fast-moving environment and is excited by leading breakthrough scientific discovery efforts. Responsibilities:Program General Management & Accountability • Own program success for one or more programs focused on discovery, process development, or production workstreams., • Design high throughput and other technology-led methods for screening, discovery, and process engineering., • Drive alignment across stakeholders and executive leadership and ensure crisp decision-making, escalation, and accountability., • Own budgeting, forecasting, and analytics of managed programs. Cross-Functional Orchestration & Execution, Communications, • Build and maintain integrated program plans that connect complex biological systems with, for example, hardware and software systems, ensuring dependencies and critical paths are explicit and managed., • Define program architecture at the "system level" (workstreams, interfaces, handoffs, validation strategy), and ensure teams execute to an integrated schedule., • Lead execution across science, engineering, lab and greenhouse operations, —coordinating interdependent projects into a single coherent program plan., • Directly manage and drive execution of cross functional program team members., • Proactively identify bottlenecks and unblock teams through clear prioritization, fast follow-through, and structured problem-solving., • Create clear communication artifacts for diverse audiences—from technical deep dives to executive summaries.Tech- and AI-Led Program Management, • Use modern tooling—including AI—to accelerate planning, synthesis, execution, communication and documentation., • Promote practical AI adoption within the program team (e.g., structured decision logs, automated status synthesis, faster technical writing), while maintaining high standards for accuracy and traceability.Qualifications:, • 2-8+ years experience leading complex, cross-functional programs or portfolios (R&D, biotech, agriculture, engineering, or related), with clear accountability for outcomes., • Strong technical foundation and systems thinking: comfort operating across biology + hardware + software/data and synthesizing ambiguity into executable plans., • Experience developing and utilizing high throughput automated screening and workflows., • Understanding of molecular biology, cellular systems, or plant biology., • Demonstrated ability to manage cross-functional workstreams and deliver against timelines, milestones, and stakeholder commitments typical of program management roles., • Proven excellence in communication—able to influence without authority, negotiate tradeoffs, and create alignment across technical and non-technical stakeholders., • High ownership, intrinsically motivated leader who is energized by mission-driven work and holds a high bar for follow-through., • Tech savvy, with strong AI utilization habits and comfort adopting new tools quickly., • Bachelor's degree required; advanced degree in life sciences, engineering, computer science, or similar is a plus. The anticipated base pay range for this role is $120,000 - $190,000 per year for our South San Francisco location, which represents several levels for this function. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, budget availability, internal equity, geographic location and external market pay for comparable jobs. About Ohalo: Ohalo™ aims to accelerate evolution to unlock nature's potential. Founded in 2019, Ohalo develops novel breeding systems and improved plant varieties that help farmers grow more food with fewer natural resources, increasing the yield, resiliency, and genetic diversity of crops to sustainably feed our population. Ohalo's breakthrough technology, Boosted Breeding™, will usher in a new era of improved productivity to radically transform global agriculture. For more information, visit www.ohalo.com. Notes: If you previously applied for a job at Ohalo Genetics, we encourage you to restate your interest in the position by submitting your application. Ohalo is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity or any other factor protected by applicable federal, state or local laws. Ohalo is also committed to working with and providing reasonable accommodations to individuals with disabilities. Please let your recruiter know if you need an accommodation at any point during the interview process. No visa sponsorship is available for this position at this time. This organization participates in E-Verify. Posters linked here. No recruiters, please.

Job DescriptionA Bit About Us: We are Arcadia Science, an evolutionary biology company founded and led by scientists. Our mission is to turn natural innovations into real-world solutions by developing systematic and quantitative approaches to leveraging biology for therapeutics R&D. We share our research as openly as possible to accelerate discovery and make our work broadly useful. The Opportunity: We’re closing the gap between biological data and biological understanding. Our Validation team does this by closing the design–build–test–learn loop through lab validation across diverse organisms. Read more about our work through our publications. We are seeking a Protein Designer to join our Validation team. In this role, the Protein Designer will work cross-functionally to run experimental loops aimed at validating our novel protein design tools. The scientist in this role will work to independently plan protein design projects, apply our tools and their ideas to generate proteins, and evaluate the biological function of the proteins they design both in vitro and in vivo. Our ideal candidate should have deep knowledge of proteins and how they function in a cellular context, as well as hands-on experience related to running design–build–test–learn loops. They are energized by evaluating novel biology, skilled at troubleshooting, and thrive in collaborative and open research environments. Enthusiasm and participation in open science is also required as we routinely share our findings via our open-source pubs. Key Responsibilities: Independently design, plan, and execute projects related to protein design Coordinate and drive design-build-test-learn loops to evaluate protein design tools Experimentally validate novel proteins in the lab (in vitro or in a cellular context) Collaborate cross-functionally with computational and experimental scientists Contribute to the development and improvement of analyses, tools, and methodologies related to protein design and the evaluation of novel proteins Synthesize ideas, data, and findings into fully open-access pubs and engage with the scientific community to maximize impact and garner feedback that improves the work Qualifications: PhD or equivalent experience in biochemistry, biophysics, bioengineering, or related field At least 3 years post-PhD or equivalent experience in a related position Deep understanding of protein function in the cell, biology, and structure and how these might be useful for protein design Experience with validation, design-build-test-learn loops, or something similar Familiarity with SOTA protein analysis and design tools (e.g., ESM, Rosetta, etc.) Experience with protein biology, biochemistry, or cell biology to inform protein expression and purification, assay development, experimental design, etc. Experience in at least one programming language and experience with relevant libraries High level of autonomy and critical thinking skills Written and oral communication skills and a willingness to share research openly, early, and often Experience working with cross-functional teams with different working styles and types of expertise Compensation: Successful applicants can expect to be compensated between $130,000-$180,000 with benefits and a highly competitive equity offering, depending on experience level. The position will require the individual to be on-site at our Emeryville, California headquarters. Application Process: Interested applicants should apply using the link below. Arcadia is an equal opportunity workplace; we welcome people from all backgrounds and communities. We provide competitive compensation and practical benefits to keep you happy and healthy so that you can do your best work. Please note that an offer of employment at Arcadia is contingent upon the successful clearance of a reference and background check.

Job Description About the job Mercor connects elite creative and technical talent with leading AI research labs. Headquartered in San Francisco, our investors include Benchmark, General Catalyst, Peter Thiel, Adam D'Angelo, Larry Summers, and Jack Dorsey. Position: Biology PhD Expert Type: Contract Compensation: $80–$150/hour Location: Remote Role Responsibilities • Evaluate the technical quality and scientific reasoning across biology, chemistry, and translational research domains., • Review research outputs in discovery and applied science workflows., • Provide structured feedback to improve scientific rigor and research outputs., • Collaborate with subject matter experts to ensure consistency and relevance in datasets., • Work independently and asynchronously to meet deadlines and enhance AI model performance. Qualifications Must-Have • PhD in Biology, Chemistry, Biochemistry, Computational Biology, Translational Science, or related fields., • Meaningful publication history in peer-reviewed research., • 2+ years of industry experience in biotech, pharma, or related R&D settings., • Strong critical thinking and scientific communication skills. Preferred • 4+ years of industry experience., • Based in the United States, United Kingdom, Canada, or Europe. Application Process (Takes 20–30 mins to complete) • Upload resume, • AI interview based on your resume, • Submit form Resources & Support • For details about the interview process and platform information, please check: https://talent.docs.mercor.com/welcome, • For any help or support, reach out to: support@mercor.com PS: Our team reviews applications daily. Please complete your AI interview and application steps to be considered for this opportunity.

Job DescriptionDescription: • Assist in the creation of the Bill of Materials for the upstream process., • Assist in development and creation of the upstream process., • Monitor upstream operations (including trouble shooting and diagnosis of instruments, equipment, process, etc.), • Set-up, prepare, and operate manufacturing equipment/labware/assemblies (includes scaleup, bioreactors, harvest filtration including centrifugation, autoclave/sterilizer, bench top meters (pH/conductivity/osmometer), etc.) in accordance with current good manufacturing practices (cGMP)., • Based on business needs there will be some cross training to support upstream operations (includes filtration skid, chromatography skid, viral filtration skid, TFF skid, Bulk fill, Freeze/Thaw, etc.) in accordance with current good manufacturing practices (cGMP)., • Record and document procedures with detail and accuracy. This includes batch records, training records, logbooks, standard operating procedures (SOPs) and validation protocols., • Execute quality systems (including critical work orders, document change requests, change control, deviations, corrective action preventative action (CAPA))., • Create and revise standard operating procedures, batch records, part numbers, specifications, etc., • Weigh and prepare culture media, feeds, buffers, and solutions., • Coordination and collaboration of activities with other departments, and with external vendors., • Sample solutions and perform analytical assays (including cell counts, pH, conductivity, etc.), • Perform technical training for staff (including hands-on and class-based training), • Assist CMC team with technical transfer activities., • Identify and implement equipment and process improvements., • Maintain clean room work areas (including floors, benches, bioreactors, chromatography skids, etc.) waste disposal, lean manufacturing and good manufacturing practices (GMP)/compliance.Requirements:, • 4 years of college science in Cell Biology, Biochemistry, Chemistry, Biology, with 2 to 4 years of related experience., • Or 4 to 8 years of experience and/or training, or equivalent combination of education and experience., • Proficiency of upstream equipment (scaleup, bioreactors, harvest filtration, flow/UV/pH/conductivity/etc. sensors), filtration equipment, solution preparation equipment (laminar air flow hood, agitator mixers, bench top instruments) are essential for this position., • Attention to detail and accurate record keeping and documentation is mandatory in this position., • Teamwork and communication are key attributes needed for this position. A collaborative attitude and a positive work ethic are key traits for success., • Flexible work hours as business requires.

Job Description Direct Counsel is seeking a Corporate Associate Attorney (Licensing) to join a leading Am Law 100 firm in its San Diego, San Francisco or Boston office. This is an outstanding opportunity for an associate attorney interested in sophisticated licensing, commercial contracting, and technology transactions within the life sciences, biotechnology, pharmaceutical, medical device, and software sectors. About the Role The Licensing & Technology Transactions team works closely with cutting-edge companies developing groundbreaking technologies and therapeutics. As a Corporate Associate Attorney, you will draft and negotiate complex commercial agreements, support strategic corporate transactions, and advise clients on intellectual property, regulatory considerations, and deal structures across all stages of the product and company lifecycle. This role offers substantial client contact, the ability to interact with scientists and business leaders, and meaningful responsibility on impactful transactions. What You’ll Do Draft, review, and negotiate a broad range of commercial agreements, including: Licensing, collaboration, development, and research agreements Clinical trial, manufacturing, supply, and service agreements Patent license agreements and IP assignments Material transfer agreements, NDAs, and distribution agreements Strategic alliance and commercialization arrangements Advise clients on contract interpretation, risk assessment, and compliance issues Conduct due diligence on IP assets and contractual obligations in corporate transactions Review high-volume commercial documents such as confidentiality agreements and terms and conditions Collaborate with scientists, executives, and cross-functional business teams to align legal strategies with operational and commercial goals Stay current on regulatory and legal developments affecting life sciences and technology transactions What We’re Looking For A highly skilled Associate Attorney with 3+ years of experience drafting and negotiating commercial contracts for life sciences or technology clients Strong understanding of intellectual property issues, including patents, trademarks, trade secrets, and copyrights Experience with software licensing, SaaS agreements, and technology transactions preferred Familiarity with data privacy considerations and emerging issues involving AI Excellent negotiation, communication, and problem-solving skills Ability to manage competing priorities, meet deadlines, and maintain exceptional attention to detail A collaborative mindset and professionalism when working with clients, colleagues, and cross-disciplinary teams Qualifications JD or LLM from an ABA-accredited law school Admission to practice in California (or eligibility to sit for/admit via reciprocity) Background in biology, immunology, biochemistry, or a related scientific field strongly preferred Experience supporting biotechnology, pharmaceutical, medical device, digital health, or related technology clients Compensation & Benefits The annualized salary range for this Associate Attorney position is $260,000 – $310,000, depending on experience and other permitted job-related factors. Attorneys are bonus-eligible and receive access to a comprehensive benefits package.

Job DescriptionSalary: $105K-$115K, depending upon experience Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to support the life sciences industry with specialized laboratory services delivered by professional scientistsadvancing research, fostering collaboration, and accelerating innovation with quality and a commitment to excellence. 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, attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment. This position may include relocation benefits as well. 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 Expert Pharma Discovery Biologist. Job duties include, but are not limited to: • Leading in vitro discovery biology across oncology programs, from early target validation through candidate selection, spanning multiple therapeutic modalities., • Contributing to target identification and prioritization by integrating literature, pathway biology, and emerging clinical and preclinical data to nominate and validate novel therapeutic targets., • Designing and executing cell-based assays to evaluate compound activity, including viability, proliferation, and apoptosis readouts across relevant tumor models., • Driving mechanistic and signaling studies (e.g., Western blot, phosphoproteomics, pathway analysis) to characterize target engagement and mechanism of action., • Leading target biology efforts including evaluation of target expression, antigen density, receptor internalization, intracellular trafficking, and target-dependent processing., • Developing and optimizing disease-relevant in vitro models (e.g., 3D culture systems, model generation, co-culture platforms) to characterize novel modalities and enable translational studies. Job requirements include, but are not limited to: • PhD in Molecular Biology, Biochemistry or related field with 0-2 years of industry or relevant postdoctoral experience in oncology drug discovery or targeted therapeutics research., • Excellent communication skills verbal and written., • Works well both within a team and as an individual., • Demonstration of excellent team player and collaboration 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 is a day shift position (approx. 8a-5p local time). Cogent Scientific provides equal employment opportunities to all applicants and does not discriminate based on any legally protected characteristic. Additionally, if you require a reasonable accommodation during the application or interview process, please let us know. This job posting will close by 7/6/2026 or when a candidate is identified, whichever comes first.

Job Description About the Role We are seeking a motivated and detail‐oriented Recruiter to support candidate delivery and sourcing efforts within the biotechnology, life sciences, and pharmaceutical space. This role will focus on identifying, engaging, and supporting high‐quality scientific and technical talent while partnering closely with internal teams to meet hiring goals. Key Responsibilities • Source and engage candidates across the biotechnology, life sciences, and pharmaceutical industries, • Support candidate delivery throughout the recruiting lifecycle, from initial outreach through offer stage, • Conduct resume reviews and initial candidate screenings, • Partner with hiring managers and internal stakeholders to understand role requirements and priorities, • Maintain accurate candidate records and recruiting documentation, • Provide administrative support related to recruiting activities, reporting, and scheduling, • Contribute to continuous improvement of sourcing strategies and recruiting processes Qualifications • Experience recruiting within biotechnology, life sciences, or pharmaceutical environments, • Analytical understanding of early research disciplines, including biochemistry or related scientific fields, • Strong analytical and problem‐solving skills, • Sales‐oriented mindset with the ability to actively source, influence, and close candidates, • Excellent administrative and organizational skills with strong attention to detail, • Proficiency with spreadsheets, databases, applicant tracking systems, and technology tools, • Strong communication skills and professional demeanor What We Offer • Salary of $55,000-$60,000, with uncapped commission potential, • Opportunity to work in a fast‐paced, growing industry, • Exposure to cutting‐edge biotechnology and pharmaceutical research rolesCompany 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 DescriptionA Bit About Us We are Arcadia Science, an evolutionary biology company founded and led by scientists. Our mission is to turn natural innovations into real-world solutions by developing systematic and quantitative approaches to leveraging biology for therapeutics R&D. We share our research as openly as possible to accelerate discovery and make our work broadly useful. The Opportunity We’re closing the gap between biological data and biological understanding. Our Validation team does this by closing the design–build–test–learn loop through lab validation across diverse organisms. Read more about our work through our publications. We are seeking an Evolutionary Cell Biology Fellow to join our Validation team for a 3-month fellowship. This is an ideal opportunity for scientists in the final stages of their PhD or postdoc training who want to experience industry research in an open science environment working with diverse organisms, or for researchers excited to apply cell biology techniques across the tree of life. Evolutionary Cell Biology Fellows will generate phenotypic and genotypic data to compare cellular features across organisms. Because we use evolution to select the best organism to study each biological question, fellows will work with diverse, often non-traditional organisms and cell types. Fellows will contribute to a defined project with the goal of publishing their work openly by the end of the fellowship. Areas of Focus We are looking for candidates with expertise in one or more of the following areas: • Cell-based or organism-based assay development and optimization- Live cell imaging, high-content screening, or other high-dimensional phenotyping approaches- Diverse cellular organism and system development and/or utilization (including non-model organisms)- Molecular biology techniques (cloning, transformation, PCR, genetic manipulation, protein detection)- Protocol development and adaptation for new organisms or cell types- Comparative analysis between species driven by evolutionary information- Quantitative approaches to phenotypic measurementWhat You'll Do, • Develop, adapt, and optimize experimental workflows for gathering phenotypic data across diverse cellular and organismal systems, • Validate platform tools and test predictions using cell-based or organism-based assays, • Troubleshoot experimental challenges independently and creatively, • Collaborate with cross-disciplinary teams to contribute to shared research goals, • Keep detailed experimental records and standard operating procedures (SOPs), • Publish results openly by the end of the fellowshipQualifications, • PhD in Cell Biology, Molecular Biology, Biochemistry, or a related field, • Demonstrated hands-on expertise in cell or organism-based assay development, • Proficiency with core cell biology tools and techniques, • Comfort with core molecular biology tools and techniques, • Comfort working with diverse cellular organisms and systems, • Familiarity with data analysis using Python or R is preferred, • Strong written and verbal communication skillsFellows will receive a competitive monthly stipend. Travel and relocation support is available for candidates relocating temporarily to the Bay Area.What We Look For The first thing we look for is technical talent at the leading edge of a field. To us, this means independent and generative scientists doing basic research that has the potential to produce evidence challenging standard practices. This is true for all of our roles: whether someone is an individual contributor or a people manager, we want researchers pushing their field forward. We're looking for hands-on, inventive scientists with deep experience in cell biology and a strong interest in using biological diversity as a tool for discovery. The ideal candidate is energized by exploring new biology, skilled at troubleshooting, and excited to work in a collaborative, open research environment. We try to develop novel approaches for every aspect of our science, and everyone on our team is expected to innovate in their domain. This is not easy, and won't be for everyone. We believe a culture where this is possible stems from how we act. Location This fellowship is on-site at our Emeryville, California lab and office for the full 3-month duration. For qualified candidates, we are willing and able to sponsor visas and provide a travel/relocation stipend if needed. Application Process Interested applicants should apply using the link. We expect to review applications at a monthly cadence. Due to anticipated volume, we may not be able to respond to all applicants. If you advance beyond initial review, we will let you know.

Job Description The QC Specialist (Data Review & Investigations) is responsible for supporting Quality Control laboratory operations through comprehensive data review, laboratory investigations, deviation management, and GMP documentation activities in a Cell & Gene Therapy environment. This role ensures laboratory testing, data integrity, and documentation comply with current GMP regulations, internal procedures, and regulatory expectations. The individual will work cross-functionally with QC, QA, Manufacturing, MSAT, and Validation teams to support clinical and commercial manufacturing activities. Key Responsibilities - Data Review & Documentation Perform detailed reviews of analytical and microbiological laboratory data for accuracy, completeness, compliance, and data integrity. Review laboratory notebooks, worksheets, electronic records, chromatographic data, calculations, and supporting documentation. Ensure compliance with cGMP, GDP, ALCOA+, and internal procedures. Support review and approval of: Raw Materials data In-process testing Release testing Stability testing Method transfer documentation Qualification and validation protocols/reports Verify laboratory investigations, deviations, and OOS/OOT documentation are scientifically sound and properly documented. Support batch disposition activities through timely QC documentation review. Key Responsibilities - Investigations & Deviations: Lead and/or support laboratory investigations including: OOS (Out of Specification) OOT (Out of Trend) Deviations Invalid Assays Atypical Results CAPAs Conduct root cause analysis using scientific and risk-based approaches. Collaborate with cross-functional teams to identify corrective and preventive actions. Track investigation timelines and ensure closure within established metrics. Support implementation and effectiveness checks of CAPAs. Education and Experience: Bachelor’s degree in Biology, Microbiology, Biochemistry, Chemistry, Biotechnology, or related scientific discipline. Advanced degree is a plus. Minimum 3–5 years of GMP Quality Control experience in biotechnology, pharmaceutical, or Cell & Gene Therapy industry. Experience with laboratory investigations, deviation management, and GMP data review required. Experience supporting clinical and/or commercial manufacturing environments preferred. Familiarity with Cell & Gene Therapy processes and aseptic manufacturing preferred. Strong attention to detail and organizational skills. Excellent written and verbal communication skills. Ability to work in a fast-paced GMP environment. Strong collaboration and teamwork mindset. Ability to prioritize multiple assignments and meet timelines. Problem-solving and critical-thinking capabilities. About GeneFab GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 with a vision to combine industry leading expertise in synthetic biology with advanced cGMP capabilities in order to accelerate the development and commercialization of genetic medicines. GeneFab offers its customers an extensive technology platform and know-how that spans early stage product design, technical development, and cGMP compliant production. GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies. We are committed to an inclusive and diverse GeneFab. We believe that different perspectives lead to better ideas, and better ideas allow us to better understand the needs and interests of our diverse GeneFab team. We welcome people of different backgrounds, experiences, abilities, and perspectives and are an equal opportunity employer. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job DescriptionSalary: $105K-$115K, depending upon experience Cogent Scientific, an insourced contract research organization, is looking for the right people to accomplish our Mission: to support the life sciences industry with specialized laboratory services delivered by professional scientistsadvancing research, fostering collaboration, and accelerating innovation with quality and a commitment to excellence. 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, attractive benefits (such as medical/dental/vision insurance; 401(k); parental leave; PTO and paid holidays; etc.) and an exciting work environment. This position may include relocation benefits as well. 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 Expert Protein Biochemist. Job duties include, but are not limited to: • Performing high-throughput molecular cloning and DNA purification as well as purifying proteins using affinity resins., • Executing batch protein expression and purification as well as column chromatography including SEC, CEX, AEX, and HIC., • Troubleshooting instrumentation is required., • Experience in the operation of AKTA FPLCs preferred., • Performing biophysical characterizations, Octet, ELISA, cellular bioassays, and FACS screens as needed., • Demonstrating collection and thorough analysis of data, and updating Electronic Notebook records. Job requirements include, but are not limited to: • PhD in Biology, Biochemistry or related field with 0-2 years of experience working in an academic or industry laboratory setting., • Excellent communication skills verbal and written., • Works well both within a team and as an individual., • Demonstration of excellent team player and collaboration 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 is a day shift position (approx. 8a-5p local time). Cogent Scientific provides equal employment opportunities to all applicants and does not discriminate based on any legally protected characteristic. Additionally, if you require a reasonable accommodation during the application or interview process, please let us know. This job posting will close by 7/6/2026 or when a candidate is identified, whichever comes first.

Job DescriptionCompany Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description AbbVie is searching for an in-house Associate General Counsel for our IP Strategy group, part of AbbVie’s Intellectual Property, Transactions, and Innovation legal team. This position will support AbbVie’s pharmaceutical products and be based in our offices in North Chicago, IL, South San Francisco, CA or Waltham, MA with a hybrid work model (on site 3+ days/week). Acting individually and in cross-functional teams, the in-house Associate General Counsel will develop and implement intellectual property strategies for AbbVie’s products and product candidates. Responsibilities: • Generate and implement intellectual property strategies across a variety of therapeutic areas and technologies, including both large and small molecules, • Partner with IP Prosecution to draft, file, and prosecute strategically useful patent applications worldwide both directly and through management of outside counsel, • Work directly with scientists to generate novel intellectual property maximizing AbbVie’s competitive position, • Provide legal advice and counsel to cross-functional R&D and business teams on a variety of IP-related matters, • Challenge and defend patents in IPR, opposition, interference, and other post-grant proceedingsQualifications, • JD degree from an accredited law school, state bar admission enabling in-house practice (specific state not required), and registration to practice before the USPTO, • 7+ years of experience practicing patent law as an attorney or patent agent at a law firm and/or life sciences company, including substantial U.S. and foreign patent prosecution, • Patent litigation experience is a significant plus, • Technical background relevant for pharmaceutical patent prosecution, such as:, • Experience with small molecule and/or biological pharmaceutical discovery & development, and/or, • Technical degree in relevant field, such as molecular biology, biotechnology, biochemistry, biology, chemistry, chemical engineering, or biomedical engineering, • Strong legal, analytical, communication, collaboration, and people skills, • Demonstrated ability to manage complex projects to meet deadlines Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

Job DescriptionDescription: ABOUT THE COMPANY Marea Therapeutics is a clinical-stage biotechnology company based in San Francisco with a growing pipeline of first-in-class therapies to address genetically validated cardioendocrine disease targets. Our therapies have the potential to complement existing therapies and serve as transformative treatment options for significant patient populations living with cardioendocrine diseases. Incubated by Third Rock Ventures, Marea completed a Series B financing in June 2024 and is well funded by a syndicate of leading life science investors including Sofinnova, Forbion, Xontogeny/ Perceptive Advisors, venBio, Omega Funds, Surveyor, Alpha Wave and Third Rock Ventures. The company’s lead program, MAR001, is a monoclonal antibody targeting ANGPTL4, a genetically validated target with potential to address the subset of patients at the highest risk of adverse cardiovascular events, despite current standard of care therapies. MAR001 is rapidly progressing through Phase 2b clinical development. Our second clinical asset, MAR002, is a monoclonal antibody targeting excess growth hormone produced by the pituitary gland in the rare hormonal disorder, acromegaly. MAR002 has potential to become best-in-disease and is rapidly progressing through Phase 1 clinical development. We also have a third asset that is rapidly advancing through research discovery, with DC nomination expected next year. At Marea, we believe in the power of collaboration and the importance of leading by example. We are a tight-knit team that values the contributions of every member, from interns to senior leaders. Our environment is dynamic, with each day presenting new challenges and opportunities for growth. Every role is “Hands-On”, and the successful candidate will be able to work alongside team members, regardless of level, to understand challenges and drive results. ABOUT THE ROLE This is a key role within the first phase of hiring for our Technical Operations team as we aggressively advance the first program towards late-stage development and our second program into early-stage clinical development, with additional programs in discovery. This role will report to the CTO. The successful candidate will oversee formulation development, drug product development and manufacturing, transition from vials to prefilled syringe for all of Marea’s development programs. Successful candidate will develop CMC strategy for formulation and drug product working cross functionally across other technical operations functions and also work closely with clinical development, clinical operations and program teams to ensure that the product profile and configuration is consistent with the target profile needed for the clinical study and ultimately for commercial launch. In addition to the strategic responsibilities, candidate will have operational responsibility to provide technical and day-to-day oversight of our CDMOs and other external partners conducting formulation and drug product development and own critical technical decisions around formulation selection and drug product presentations for the entire portfolio. Candidate will also plan future tech transfer and drug product manufacturing strategy, develop and execute life cycle plans and ensure these are integrated into the cross functional project team as well as the financial operating plans. While the role is primarily focused on formulation and drug product development, this is a leadership role that is expected to influence and guide the overall CMC development especially considering that many of the CMC challenges for our portfolio products are centered on formulation and drug product. The scope of the role will also include discovery programs, that are expected to approach drug candidate nomination, where the candidate is expected to provide molecular and formulability assessment, and biophysical characterization, to impact the selection of the candidate molecules. The role is also expected to contribute to drug product comparability and analytical characterization as part of the CMC life cycle management. This role is viewed as a senior member of the technical operations team and will be a keep voice in guiding the evolution of the department with respect to CMC strategy and the growth of the team in anticipation of various strategic scenarios. As such, the scope of this role is expected to evolve accordingly. Requirements: KEY RESPONSIBILITIES · Accountable for formulation and drug product development strategy and execution for the entire Marea portfolio which includes monoclonal antibodies in early and late-stage CMC development and other modalities in discovery. · Develop a holistic drug product, formulation and device strategy for each of Marea’s asset keeping in mind clinical/patient experience, commercial opportunity and regulatory considerations. · Design/execute (with the external CDMO partner) pre-formulation and formulation studies with a focus on stability, manufacturability, and patient-centric delivery. · Develop scalable drug product processes for all formulations; lead scale-up and tech transfer to CDMOs. Provide technical oversight of the operations at the CDMOs · Drive development of combination products, including pre-filled syringes; experience with autoinjectors is a strong plus. · Author/review CMC sections of regulatory document (ex., INDs, IMPDs, and BLAs). · Partner closely with internal stakeholders (Analytical, Process Development, Quality, Regulatory, Clinical) to ensure cross functional alignment of key assumptions around formulation and drug product · Manage external partners (CDMOs, CROs) to execute formulation and fill-finish activities, including oversight of timelines, budgets, and technical deliverables. · Identify, plan and complete necessary product and container compatibility, leachables and extractables studies necessary for the stage of the regulatory submission · Contribute strategically and scientifically to CMC planning and risk mitigation across programs. · Be hands-on where needed and adaptable to the evolving needs of a dynamic startup environment. · Oversee tech transfer and manufacturing of drug product manufacturing at CDMOs · Lead and deliver process characterization and validation studies leading upto the BLA, including other BLA enabling activities related to drug product and formulation · Collaborate with discovery teams for early molecular and formulability assessment to guide selection of future drug candidates · Identify and generate drug product comparability and analytical characterization as part of the CMC life cycle management KEY QUALIFICATIONS · PhD or MS in Pharmaceutics, Biochemistry, Chemical/Biomedical Engineering, or related field. · 15+ plus years (PhD) of relevant industry experience in formulation and drug product development of biologics. · Deep understanding of protein formulation principles, stability challenges, and container/closure compatibility · Solid understanding of various drug product configurations including vials, prefilled syringe (Autoinjector familiarity a plus) · Experience in early-phase development (preclinical/IND) with strong knowledge of regulatory expectations; late-stage/BLA experience is a plus. · Demonstrated success working in fast-paced, resource-constrained environments with a solutions-first mindset. · Strong communication skills and ability to work across disciplines and with external partners. · Comfortable wearing multiple hats and contributing both strategically and tactically. PAY RANGE The salary range for this role is $275,000 - 315,000. Compensation and title will be competitive and commensurate with the candidate's experience, qualifications, and the responsibilities of the position. WORKING CONDITIONS · The role may need to occasionally work in laboratory environment. · Travel to CDMOs/CTLs may be needed up to 10% of the time (variable, with some peak windows) We do not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual’s status in any group or class protected by applicable federal, state, and local law. We invite applications from minorities, women, the disabled, protected veterans, and all other qualified applicants.

Based in South San Francisco, Mission Bio is the leader in single cell multi omics solutions for precision medicine. Our mission is to empower researchers and clinicians to eradicate cancer, and our Tapestri® Platform is at the center of that effort. As the industry’s first high throughput single cell multi omics solution, Tapestri is trusted by leading academic medical centers, cancer institutes, and biopharma companies to advance research and accelerate the development of curative therapies, including the future of cell and gene therapy. Following a successful equity financing round led by Ally Bridge Group, we are entering an exciting growth phase focused on innovation, deeper commercial partnerships, and broader clinical adoption. Our expanded tri omics capabilities now combine targeted gene expression and genotyping in a single assay, opening up new opportunities across oncology and therapeutic development. We are a dynamic and diverse team that lives by the culture of One Cell. One Team. One Vision. We are collaborative, driven, and deeply curious. These values fuel our innovation and unite us in our mission. As Senior Product Manager, you’ll drive groundbreaking single-cell product launches, guide cross-functional execution, and mentor a Product Manager to directly influence our growth and the future of cancer treatment. What you'll do: • Lead commercialization of new product introduction, representing flagship product offering for Mission Bio, • Manage existing products for Tapestri platform including instrument, reagents, software, • Build financial models to support commercialization process and strategy around product offering and clinical utility Conduct voice of customer and sales to understand customer needs and market segments to define product roadmap, • Positioning of product offering across different applications across heme oncology and cell and gene therapy and customer segments, • Conduct competitive analysis of orthogonal technologies offering across different market segments including NGS and other single cell technologies, • Collaborate with cross functionally to generate proof points, marketing collateral and sales trainings, • Lead and mentor a Product Manager to deliver on product strategy and execution Required Skills, Education and Experience: • Minimum requirement: MS. A Ph.D / MS in Molecular Biology / Cell Biology / Biochemistry discipline is preferred., • Minimum of 3-5 years of relevant product management experience, with at least 1-2 years in the genomics space., • Experience in defining and executing robust product initiatives, including understanding, and gathering of customer requirements, MVPs, building ROI models to support product commercialization process, is required., • Experience in product management leadership across core teams to guide program priorities, balance customer experience with revenue growth, is required., • Experience in programs involving overall system improvements such as reagents, software, and instrument system, is required., • Proven ability in working closely with FAS, R&D and operations to prioritize sustaining issues and enable customer success and strengthen core business is a plus., • Experience in product development process, NPI's to build ROI models is preferred., • Understanding of single cell market, next generation sequencing is a definite plus., • Deep understanding of genomics, heme oncology cell, and gene therapy, and in techniques such as NGS, PCR, IHC, Flow Cytometry would be a definite plus., • Experience w applications including Cell and Gene Therapies, heme-oncology, immune-oncology, • Self-motivated team player with ability to effectively manage competing multiple priorities and tight timelines. What can Mission Bio off you? The base salary for this role is between $165,000 - $190,000/annual depending on experience. Additional Benefits We Offer: • Participation in the company’s employee incentive plan, which ensures eligible employees participate in the upside upon a liquidity event, • Comprehensive benefits for U.S. employees, including medical, dental, and vision insurance, pre-tax commuter options, and a 401(k) plan, • Flexible working hours and an unlimited vacation policy to support personal well-being and productivity, • Training and professional development opportunities, including dedicated time with your manager to define growth goals and expand your expertise Mission Bio is an equal opportunity employer. We welcome and encourage diversity in the workplace regardless of race, gender, sexual orientation, gender identity, disability or veteran status or any other characteristic protected by federal, state or local laws.

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