• Project Manager I

    Charles River Laboratories (Northridge, CA)
    …multiple high-impact projects simultaneously. Experience in client communication, regulatory environments, and process improvement is highly desirable. Essential ... across internal workflows. + Collaborate with departments such as R&D, Quality, Regulatory , and Manufacturing to meet project goals. + Ensure projects adhere to… more
    Charles River Laboratories (08/08/25)
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  • Pharmacy Program Coordinator - Supply Chain

    Cedars-Sinai (Beverly Hills, CA)
    …Expertise:** Oversee and manage the pharmaceutical supply chain, including drug shortage management, liaison activities with key partners (Vizient, McKesson, ... financial performance through dashboard creation. This includes responsibility for contract proposal analysis and negotiation. + **Program Development and… more
    Cedars-Sinai (06/14/25)
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  • Manager, IT Business Analysis - R&D IT Research…

    Gilead Sciences, Inc. (Foster City, CA)
    …request for proposal (RFP) submissions and responses, evaluate vendors, and ensure contract readiness, including compliance with regulatory requirements like GxP ... in design reviews, contributing to the development of digital solutions that enhance drug development efforts. + Oversee and manage the creation of test scenarios,… more
    Gilead Sciences, Inc. (08/09/25)
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  • Regional Director, Field Operations

    Transdev (San Francisco, CA)
    …diverse roles. + Demonstrated success in managing safety, quality control, and regulatory compliance. + Strong client-facing communication skills with the ability to ... Requirements: + All Transdev employees must satisfactorily complete a pre-employment drug screen and background check. Safety Sensitive Positions will also be… more
    Transdev (07/21/25)
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  • Senior Buyer

    Solar Turbines Incorporated (San Diego, CA)
    …issue resolution, communication of demand and forecasts, preparing contracts, negotiating contract terms, providing solutions to a wide range of issues, managing ... include: Supply Chain Management - Ensures procurement processes meets audit, regulatory , and legal standards. Develops and maintain relationships with internal… more
    Solar Turbines Incorporated (08/24/25)
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  • As-Needed Environmental Compliance Analyst

    Dudek (CA)
    …to compliance managers and other field staff to ensure project adherence to regulatory permit requirements. This position has the opportunity to work on an extensive ... resource leads and environmental compliance managers to meet compliance monitoring regulatory requirements. + Oversee the preparation of compliance deliverables that… more
    Dudek (08/21/25)
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  • Executive Director of R&D Global Quality (Remote)

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …trial and submission support, lead the R&D audit program, engage with regulatory authorities, and maintain clinical data integrity. The leader will be responsible ... audits at all relevant facilities, investigator sites, and vendors (including contract research organizations) and ensure that audit results are communicated, and… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • Senior Director, Software Engineering

    Abbott (Pleasanton, CA)
    …other regulatory requirements. + Complies with US Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating ... Institute efficient communication and cross-functional collaborations with marketing, quality, regulatory , clinical, project management, etc, at multiple levels. +… more
    Abbott (08/14/25)
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  • Vice President, Manufacturing Operations

    Vera Therapeutics (Brisbane, CA)
    …product into global markets. While working with internal teams, such as quality, regulatory , commercial, and finance, and external contract service provides, the ... regulatory requirements including authoring and reviewing BLAs and interacting with regulatory authorities. * Solid understanding of drug development within… more
    Vera Therapeutics (07/25/25)
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  • Senior Product Engineer (Northridge, CA)

    Medtronic (Northridge, CA)
    …concise, and well-structured biocompatibility evaluation plans and reports to support regulatory submissions. The Senior Product Engineer applies scientific rigor in ... including the preparation of technical protocols and reports, as well as drug compatibility studies related to biocompatibility evaluations. The role also supports… more
    Medtronic (08/16/25)
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