Senior Scientist, Downstream Process Development (Contract) - AW Adverum Biotechnologies, Inc.Senior Scientist, Downstream Process Development (Contract) - AWRedwood City, CAThe successful candidate will participate in late-stage activities including design and optimization of the process as needed using historical batch data and manufacturing needs; process characterization; and tech-transfer of downstream processes to support clinical and commercial manufacturing. Leveraging the research capabilities of its proprietary intravitreal (IVT) platform, Adverum is developing durable, single-administration therapies designed to be delivered in physicians’ offices to eliminate the need for frequent ocular injections to treat these diseases.
["QC Analyst II *PC 610","QC Analyst II *PC 610"] Miltenyi Biotec["QC Analyst II *PC 610","QC Analyst II *PC 610"]San Jose$38.75–$45.63 / hourRole OverviewThis position is primarily responsible for the complete development, qualification and performance of environmental monitoring and microbiological QC assays to support GMP manufacturing operations in a Phase I/II multi-product biologics facility. Responsibilities include development, qualification and execution of environmental monitoring processes and microbiological assays, development and review of trend reports, SOPs, batch related EM results, and other controlled documents.
Sr. Supervisor, Manufacturing Formulation Avid Bioservices IncSr. Supervisor, Manufacturing FormulationTustin, CAOperate and maintain Manufacturing production support equipment including but not limited to autoclave, depyrogenation oven, Cozzolli vial/bottle washer, Sartocheck filter integrity testers, pH/conductivity meters, Laminar Flow Hoods and Biosafety Cabinets. Minimum Qualifications: Related Bachelor's degree (i.e. Biology, Biotechnology, Chemical Engineering) plus 3 - 5 years cGMP support and formulation experience plus 1 - 3 years leadership experience or equivalent combination of experience.
NewSenior Manager / Associate Director, Regulatory Affairs Neurona Therapeutics IncSenior Manager / Associate Director, Regulatory AffairsSouth San Francisco, CAThis role spans both Clinical and CMC (Chemistry, Manufacturing, and Controls) regulatory affairs, and the ideal candidate brings a strong scientific background along with the ability to navigate the complex regulatory landscape for advanced therapy medicinal products (ATMPs) - specifically cell therapies. Author, review, and manage the preparation of high-quality regulatory submissions, including INDs, CTAs, meeting requests, briefing packages, and ultimately BLAs/MAAs.
Senior Program Manager, New Product Introduction Alamar Biosciences IncSenior Program Manager, New Product IntroductionFremont, CAThe Senior Program Manager is a key member of Alamar's PMO, partnering with leaders and subject-matter experts across the organization to drive complex new product development programs in scientific discovery and clinical diagnostics. The Senior Program Manager provides leadership to cross-functional program teams and takes ownership of program planning and delivery for mission-critical new product development programs.
Supervisor, Manufacturing Upstream (M-F Flex) Avid Bioservices IncSupervisor, Manufacturing Upstream (M-F Flex)Tustin, CA$75,000–$95,000 / yearMinimum Qualifications: Bachelors degree in biology, biotechnology, chemical engineering or related field plus 3 - 5 years cGMP upstream experience or equivalent combination of experience and education. Physical Demands & Work Environment: In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds.
Director / Senior Director Of Regulatory Operations Artiva BiotherapeuticsDirector / Senior Director Of Regulatory OperationsSan Diego, CA$205,000–$268,000 / yearThe ideal candidate will bring deep expertise in eCTD submissions, regulatory information management systems, and cross-functional project leadership in a fast-paced biotech environment, with preference for experience in cell therapy or biologics. Partner with Regulatory Affairs Leads, Clinical Development, CMC, Pharmacovigilance, Project Management and Program Lead to develop and maintain integrated regulatory project plans, timelines, and risk mitigation strategies.
R&D Informatics Analyst (Contract) 4D Molecular Therapeutics Inc.R&D Informatics Analyst (Contract)Emeryville, CA$47–$60 / hourResponsibilities include supporting lab equipment and applications (GMP and non-GMP), troubleshooting hardware and software issues, performing computer system validation activities (including change controls, validation execution, NCRs, AIRs, and CAPAs), maintaining data integrity and compliance, and administering system configuration, access management, security patching, and data backup processes. Familiarity with broad range of lab instrumentation and Enterprise IT solutions used in Biopharma, e.g., LC systems (Waters/Agilent), AKTA, SoftMaxPro, Geneious, ELN/LIMS (Sapio), Imaging Systems, Bioreactors, Plate readers, Sequencers, etc.
BioPharma Sales Executive - San Francisco Oxford Nanopore Technologies PlcBioPharma Sales Executive - San FranciscoSan Francisco, CARemote$136,000–$180,000 / yearOwn and execute deal strategy for biopharma accounts across the region, including opportunities with national or global scope, by developing account plans, mapping stakeholders and influence networks, identifying whitespace, and using technical selling to advance strategic applications and drive revenue growth. Expand Oxford Nanopore's footprint within underpenetrated biopharma accounts by engaging new teams and decision-makers and advancing applications across R&D, analytical development, and quality control, including mRNA QC, plasmid sequencing, cell line characterization, and microbial applications.
Senior Scientist, Protein Therapeutics - Mammalian Expression & Cell Line Engineering Amgen Inc.Senior Scientist, Protein Therapeutics - Mammalian Expression & Cell Line EngineeringThousand Oaks, CAIn addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients.
Associate Director, Quality Assurance (Gmp QC Lab Oversight) Coherus BiosciencesAssociate Director, Quality Assurance (Gmp QC Lab Oversight)Camarillo, CA$170,000–$200,000 / yearExperience reviewing and approving equipment and instrument qualification and validation documentation (e.g., IQ/OQ/PQ), with working knowledge of lifecycle management principles; experience applying risk-based approaches to computerized systems (GAMP 5) preferred. Qualifications: Bachelor's degree in a scientific discipline (or equivalent experience) with a minimum of 8 years of direct experience supporting GMP QC laboratory operations in a regulated pharmaceutical or biotechnology environment, including QA oversight.
Manager, Document Control and Training Jade BiosciencesManager, Document Control and TrainingSan Francisco, CaliforniaRemote$130,000–$140,000 / yearJade’s pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an undisclosed antibody candidate, both currently in preclinical development. Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases.
Customer Support Representative 503BA Nivagen PharmaceuticalsCustomer Support Representative 503BASacramento, CaliforniaThrough vertical integration of the pharmaceutical supply chain, cutting-edge technology, and unwavering dedication to excellence, we continually strive to redefine medication accessibility and affordability. Nivagen is a global company dedicated to enhancing lives by developing and providing cost-effective generic prescription drugs and over-the-counter products for the North American market.
Family Access Lead- Rare Disease BiogenFamily Access Lead- Rare DiseaseSan Francisco, California$184,000–$253,000 / yearRegular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. The base compensation range for this role is: $184,000.00-$253,000.00 Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Veterinary Cardiologist (Board Certified / Diplomate / Residency Trained) Global Talent PartnersVeterinary Cardiologist (Board Certified / Diplomate / Residency Trained)Thousand Oaks, CA$300,000–$360,000 / yearProminent features include: - An environment rich with natural beauty and outdoor recreational activities, including over 150 miles of trails and numerous parks. Additionally, staff members enjoy a robust support system, blending local leadership with centralized resources to enhance both autonomy and effectiveness.
Veterinary Radiologist (Board Certified / Diplomate / Residency Trained) Global Talent PartnersVeterinary Radiologist (Board Certified / Diplomate / Residency Trained)San Diego, CA$150,000–$310,000 / yearWith a 26,000-square-foot, AAHA-accredited facility, equipped with sophisticated imaging capabilities like CT and MRI machines, the hospital fosters a high-quality environment for both diagnostic precision and comprehensive care. San Diego, CA, known for its ideal climate and high quality of life, offers much more than just professional opportunities: - Average of 266 sunny days for year-round outdoor activities.
NewDirector, Technology Development Research Kyowa Kirin Pharmaceutical Research IncDirector, Technology Development ResearchLa Jolla, CA$190,700–$246,800 / yearThe position sets scientific direction across multiple projects and platform initiatives, ensures alignment of research execution with portfolio priorities, and develops decision-ready data packages to support downstream development, external collaboration, and future technology transfer. Summary: The Director Technology Development Research provides strategic, scientific, and technical leadership for technology research supporting cell and gene therapy programs, with a primary focus on allogeneic immune cell platforms.
Managing Consultant, Health & Safety (Biosafety Focus) ERM International Group LtdManaging Consultant, Health & Safety (Biosafety Focus)Irvine, CA$103,872–$130,886 / yearThis is an opportunity to influence how leading biotechnology, pharmaceutical, research, and high-tech organizations design and run their biosafety and health & safety programs-moving beyond compliance toward resilient, high-performing systems that enable innovation while protecting people and operations. Who We Are: As the largest global pure play sustainability consultancy, we partner with the world's leading organizations, creating innovative solutions to sustainability challenges and unlocking commercial opportunities that meet the needs of today while preserving opportunity for future generations.
Debut Internship Talent Pool Debut BiotechDebut Internship Talent PoolSan Diego, CaliforniaThe performance of this position will present exposure to an industrial environment and requires support and compliance with the published Company PPE policy including but not limited to the use of personal protective equipment such as safety glasses with side shields, appropriate attire, safety shoes, hard hat, hearing protection, etc. Occasional: walking, standing, climbing stairs, bending and twisting of neck, bending and twisting of waist, squatting, simple grasping, reaching above and below shoulder level, and occasional lifting and carrying of files or material weighing up to 50 pounds.