• CMC Biologics Quality

    Teva Pharmaceuticals (West Chester, PA)
    CMC Biologics Quality Control Director, Physiochemical Testing Date: Nov 15, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: ... CMC organization Design, plan, organize, analyze, and evaluate key elements of Biologics CMC QC strategy Specialized Knowledge: LIMS, TrackWise or VEEVA … more
    Teva Pharmaceuticals (10/18/25)
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  • Dir, Engineering, CMC Leader…

    Merck (West Point, PA)
    …(DCT) leader is accountable for delivering a fully integrated stage-appropriate CMC development and commercialization strategy which yields the target commercial ... product. The specific role will be responsible for advancing the company's biologics portfolio. Correspondingly, the DCT leader will be responsible for delivering… more
    Merck (12/09/25)
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  • Director, Biologics Analytical Development…

    Gilead Sciences, Inc. (Foster City, CA)
    …+ Recruit and hire new talent. + Accountable for: + Defining critical quality attributes (CQAs) across the late-phase biologics portfolio and building deep ... across Gilead Pharmaceutical Development & Manufacturing (PDM) and partner with Quality , Supply Chain, Manufacturing, CMC Regulatory Affairs, Clinical… more
    Gilead Sciences, Inc. (11/08/25)
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  • Senior Scientist I, Biologics Drug Product…

    AbbVie (North Chicago, IL)
    …transfer. + Experience in managing third party manufacturers. + Experience with quality risk management and drug product control strategies. Additional ... Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Biologics Drug Product Development (Bio DPD), a part of Development… more
    AbbVie (12/09/25)
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  • CMC Regulatory Affairs Senior/Consultant…

    Parexel (Providence, RI)
    …and post-approval changes Cross-Functional Collaboration * Partner with manufacturing, quality , and external organizations to address CMC -related issues ... highly motivated professional to join our Global Regulatory Affairs team as a CMC Regulatory Affairs Senior/Consultant. This role is critical to ensure our client's… more
    Parexel (10/11/25)
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  • Lead, Regulatory Affairs CMC (Director)

    Astellas Pharma (Northbrook, IL)
    Quality Assurance, Business Partners). Responsible for developing regional/global CMC regulatory strategy (eg, CMC strategy/planning for new products), ... are encouraged to apply. **Purpose and Scope:** We are seeking an experienced CMC Regulatory Affairs Director with deep expertise in the United States regulatory… more
    Astellas Pharma (12/05/25)
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  • Director, CMC

    Xeris Pharmaceuticals, Inc. (Chicago, IL)
    …Regulatory Submission support for US FDA and other Health Authorities. + Ensures all Quality by Design (QbD) and Design Control activities related to drug ... support of company clinical trials. + Collaborates with other external functions on CMC matters (eg, Quality , Commercial, Regulatory Affairs, etc.). Ensures the … more
    Xeris Pharmaceuticals, Inc. (10/30/25)
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  • Director, Regulatory Affairs CMC

    Taiho Oncology (Princeton, NJ)
    …scientific expertise in a discipline related to pharmaceutical development, manufacturing, or quality . + Fifteen years' previous CMC drug development and ... related area. + Substantial experience leading and preparing Chemistry, Manufacturing and Control ( CMC ) documentation for regulatory filings. + Experience in… more
    Taiho Oncology (12/09/25)
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  • Director, Scientific Expert CMC

    Boehringer Ingelheim (Duluth, GA)
    …alignment with corporate goals. + Defines, plans, and oversees the development of high- quality CMC regulatory submissions, with a focus on securing timely ... with Quality , R&D and Operations/Manufacturing. The Director, Scientific Expert CMC provides subject matter expertise in functional areas related to, and driven… more
    Boehringer Ingelheim (09/12/25)
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  • Scientist l, Analytical Development…

    AbbVie (North Chicago, IL)
    …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description AbbVie Biologics Analytical Research & Development ( Biologics ARD) is a ... global analytical sciences organization responsible for all CMC analytical activities related to the development of AbbVie's therapeutic biologic products. Our scope… more
    AbbVie (11/15/25)
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  • Process Development Senior Scientist - Pivotal…

    Amgen (Thousand Oaks, CA)
    …patients while transforming your career. **Process Development Senior Scientist - Pivotal Biologics Drug Substance Technology** **What you will do** Let's do this. ... at Amgen develops, characterizes and supports the commercialization of biologics drug substance manufacturing processes for all late-stage programs across… more
    Amgen (11/26/25)
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  • Senior Manager, Global External Manufacturing,…

    Gilead Sciences, Inc. (Foster City, CA)
    …Description** **Key Responsibilities** Senior Manager, Global External Manufacturing Biologics supports uninterrupted supply of Gilead's clinical and commercial ... Development and Manufacturing organization (PDM). Experience in leading the Manufacture of Biologics Drug Substance is a must. This role requires collaboration at… more
    Gilead Sciences, Inc. (10/03/25)
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  • Biologics Analytical Research & Development…

    AbbVie (South San Francisco, CA)
    …through innovative solutions. We are responsible for all Chemistry, Manufacturing, and Control ( CMC ) analytical activities related to the development of AbbVie's ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description 2026 Biologics Analytical Research & Development Intern Overview Envision spending your… more
    AbbVie (11/14/25)
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  • Biologics Analytical R&D Intern (PhD)

    AbbVie (North Chicago, IL)
    …through innovative solutions. We are responsible for all Chemistry, Manufacturing, and Control ( CMC ) analytical activities related to the development of AbbVie's ... specialized protein separation techniques to enable the analysis of product quality attributes of interest. + Troubleshoot equipment and experimental problems. +… more
    AbbVie (09/28/25)
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  • Principal Scientist, Engineering

    Merck (West Point, PA)
    **Job Description** **Principal Scientist, Biologics , Sterile Drug Product Commercialization** As part of Our Company's Manufacturing Division, the Sterile Drug ... capabilities for late stage and commercial drug product processes for vaccines, biologics , and sterile pharmaceutical products. It is the division's leader in… more
    Merck (12/10/25)
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  • Director of Quality - BioAnalytical

    Catalent Pharma Solutions (Kansas City, MO)
    Quality Unit objectives and focused on ensuring specific focus upon best-in-class Quality Control related procedures; + Maintain an effective Quality ... (QMS) that aligns with regulatory requirements/expectations, with particular focus upon Analytical and Quality Control ; + Ensure the QMS is agile and flexible to… more
    Catalent Pharma Solutions (11/11/25)
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  • Global Head of Project and Portfolio Management

    Genentech (South San Francisco, CA)
    …such as drug substance, drug product, analytical development & quality control , device and delivery, regulatory CMC , manufacturing sciences, and clinical and ... execution, CMC project management, and a team of technical development leaders ( CMC leaders) responsible for delivering high- quality , timely CMC packages… more
    Genentech (11/27/25)
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  • Program Officer, Chemistry, Manufacturing…

    Bill and Melinda Gates Foundation (Seattle, WA)
    …and partners to provide strategic and technical guidance on Chemistry, Manufacturing and Control ( CMC ) issues. You focus on products incorporating polio and ... portfolio of high-impact product development grants to achieve cost, quality , safety, and therapeutic effectiveness targets. + Assist in...in the areas outlined below. + Experience in implementing CMC solutions for a broad range of biologics more
    Bill and Melinda Gates Foundation (10/22/25)
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  • Technical Development Senior Principal Scientist

    Genentech (South San Francisco, CA)
    …Scientist position is available in Genentech's Analytical Development and Quality Control (ADQC) department for US Biologics in the Pharma Technical ... biologics pipeline. This function provides integrated analytical control strategies and systems that enable CMC ...multidisciplinary team of analytical, biological, and quality control scientists in support of the CMC more
    Genentech (09/17/25)
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  • Exec Director, Regulatory Affairs-Combination…

    Gilead Sciences, Inc. (Washington, DC)
    …A scientific degree with directly relevant professional experience in small molecule and biologics development, global CMC regulatory affairs and CMC ... devices. . **Global Regulatory Excellence** Lead the development of global CMC regulatory initiatives focused on combination products and devices. Ensure regulatory… more
    Gilead Sciences, Inc. (12/03/25)
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