• Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance , and other departments to ... **Associate Director , Small Molecule Analytical Development** + Lead and...lifecycle, including preclinical and clinical stages, regulatory requirements, and quality standards. **Competencies** **Accountability for Results -** Stay focused… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • Senior Director , MSAT Biologics

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …cost reduction where appropriate. + Collaborate with cross-functional teams including R&D, Quality Assurance , Regulatory Affairs , and Operations to align ... **Position Overview:** The Senior Director , MSAT Biologics provides strategic and technical leadership...+ Ensure compliance with cGMP regulations and other relevant quality standards + Represent the MSAT function in interactions… more
    Otsuka America Pharmaceutical Inc. (07/15/25)
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  • Oncology Early Stage Clinical Scientist…

    Pfizer (South San Francisco, CA)
    …Clinical Operations, Safety, Biostatistics, Regulatory, Study Management, Pre-Clinical, Pharmacology, Quality Assurance . + Experience building consensus and ... of clinical studies and delivering on innovative clinical study designs, high quality trial execution, safety assessment and interpretation of clinical study results… more
    Pfizer (10/07/25)
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  • Program Safety Lead, GPS Medical Science…

    Ascendis Pharma (Palo Alto, CA)
    …provide appropriate representation during PV related regulatory inspections or internal quality assurance /corporate compliance audits. . Functions as a patient ... safety advisor to Ascendis Clinical Development Organizations, Medical Affairs , Commercial Organizations and PV staff. . Provides pharmacovigilance expertise to… more
    Ascendis Pharma (07/17/25)
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  • Biomedical Scientist - Biobank Core

    Cedars-Sinai (Beverly Hills, CA)
    …and safety standards by monitoring all ongoing activities and interacting regularly with QA and Regulatory Affairs . + Leads projects, trains, and assists in ... join the team!** The Biobank and Research Pathology Resource provides high‑ quality biospecimens and equips researchers with instrumentation, expertise, and flexible… more
    Cedars-Sinai (07/30/25)
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  • Product Development Scientist

    Unilever (El Segundo, CA)
    …commercialization of all products with our co-Manufacturing partners. + Collaborate with Quality and Regulatory Affairs in the standardization of blend, raw ... material, Product stability and formulation specifications in accordance with QA /RA requirements, while meeting developmental and financial targets. + Build… more
    Unilever (09/10/25)
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