• Senior Director, US Provider Access Strategy…

    Gilead Sciences, Inc. (Santa Monica, CA)
    …in partnership with the EDs of Customer Engagement, US Medical Affairs, US Quality , and Global Analytics & Commercial Operations (GACO) and oversees the team that ... in partnership with the EDs of Customer Engagement, US Medical Affairs, US Quality , and GACO _Provider_ _Access_ _Market_ _ing_ + Oversee development of all… more
    Gilead Sciences, Inc. (08/29/25)
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  • Clinical Research Associate - IMM/Cross TA…

    ICON Clinical Research (Los Angeles, CA)
    …including selection, initiation, routine monitoring, and close-out + Ensure site compliance with ICH-GCP, SOPs, and regulations + Maintain up-to-date documentation ... + Support and track site staff training and maintain compliance records + Monitor patient safety, ensuring timely and...or destruction + Resolve data queries and drive timely, high- quality data entry + Document site progress and escalate… more
    ICON Clinical Research (08/28/25)
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  • Facilities Maintenance Planner (R&D)

    Mentor Technical Group (Redwood City, CA)
    …and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy ... operations activities. + Is responsible for overseeing work order activity compliance with respective regulatory requirements (ie FDA, DEA, OSHA). + Manage… more
    Mentor Technical Group (08/28/25)
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  • Senior Health & Science Specialist, Cardiac Rare…

    Pfizer (Sacramento, CA)
    …we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.Our science and risk-based ... compliant quality culture is innovative and customer oriented. Whether you...oriented. Whether you are involved in manufacturing, testing, or compliance , your contribution will directly impact patients. **What You… more
    Pfizer (08/22/25)
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  • Maintenance Supervisor

    Takeda Pharmaceuticals (Los Angeles, CA)
    …and executing daily maintenance activities at the LA Site while ensuring compliance with current Good Manufacturing Practices (cGMP), Environmental Health and Safety ... emergency and urgent work orders. + Coordinate and oversee contractors, ensuring compliance with site standards and requirements. + Monitor and maintain equipment,… more
    Takeda Pharmaceuticals (08/20/25)
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  • Sr. Manager, Clinical Data Management

    Terumo Neuro (Aliso Viejo, CA)
    …developing and/or enhancing data management processes to ensure complete, accurate, high quality clinical data and adhering to Good Clinical Practices and FDA ... regulations. Job duties: + Develop and implement SOPs to ensure GCP/ICH compliance for data management, database operations, clinical report writing, case report… more
    Terumo Neuro (08/19/25)
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  • Production Lead - Powder - 3rd Shift

    Fujifilm (Santa Ana, CA)
    …fosters curiosity, collaboration, and innovation, and we pride ourselves on delivering unparalleled quality and service to our partners. If you're ready to make an ... **Job Description** **Responsibilities** + Reviews completed production lot folders for compliance with current regulations and company policies and procedures. +… more
    Fujifilm (08/15/25)
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  • Maintenance Technician Senior

    Astrix Technology (Thousand Oaks, CA)
    …processes. **Qualifications:** + Strong working knowledge of GMP, CFR regulations, and quality systems in a pharmaceutical or life sciences environment. + ... areas + Develop, write, and complete a variety of technical and compliance documentation, including: + Standard Operating Procedures (SOPs) + Change Controls (CCMS)… more
    Astrix Technology (08/11/25)
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  • Senior Scientific Director, Clinical Development…

    AbbVie (Irvine, CA)
    …in and may lead cross-functional teams to generate, deliver, and disseminate high- quality data supporting consumer eye care product scientific and business strategy. ... plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and… more
    AbbVie (08/08/25)
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  • cGMP Process Development (PD) Specialist

    University of Southern California (Los Angeles, CA)
    …implements necessary changes to the process and reagents for cGMP compliance , execute technology transfer activates, identities and supports the development of ... support tech transfer of processes) from cGMP manufacturing and assays to quality control. Develops and reviews standard operating procedures (SOP), protocols and… more
    University of Southern California (06/09/25)
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