• External Affairs Senior Director

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …collaborative work environment. **Brief Job Overview** The External Affairs Senior Director- Biologics will lead USP's efforts to shape regulatory policy and engage ... and influence key stakeholders to advance USP standards for biologics products. This role will partner closely with the... products. This role will partner closely with the Biologics Division and colleagues in GEA and RPS and… more
    The US Pharmacopeial Convention (USP) (06/25/25)
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  • Utilities Supervisor

    Bristol Myers Squibb (Devens, MA)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . **Job Summary** Biologics is changing the landscape of disease treatment, and BMS is ... expanding our biologics manufacturing capacity and development. This investment is our...patients and the future of therapeutic advancements. Our state-of-the-art biologics facility spans across biologics process development,… more
    Bristol Myers Squibb (07/24/25)
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  • Senior Manager, Analytics Operations

    Bristol Myers Squibb (New Brunswick, NJ)
    …across the Bristol Myers Squibb global network. Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing ... Product Development and Supply (GPS) network as the company's first European biologics manufacturing facility. This state of the art facility will produce multiple… more
    Bristol Myers Squibb (07/16/25)
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  • Senior Principal Scientist, Upstream Process R&D

    Merck (Rahway, NJ)
    …self-motivated scientific leader with expertise in downstream bioprocessing to join Biologics Process Research & Development (BPR&D) as a Senior Principal Scientist. ... and inclusive environment. In addition to process development for pipeline biologics , we are focused on innovating and building next-generation biomanufacturing… more
    Merck (07/24/25)
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  • Director, Drug Metabolism

    Gilead Sciences, Inc. (Foster City, CA)
    …together. **Job Description** **Specific Responsibilities:** The primary responsibility of this Biologics DMPK Director position is to serve as an expert in ... the PK and PK/PD of biologics , representing the DMPK department by providing strategic and...and development as a subject matter expert for DMPK Biologics , providing PK or PK/PD expertise to the design… more
    Gilead Sciences, Inc. (07/24/25)
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  • Principal Scientist, Upstream Process R&D

    Merck (Rahway, NJ)
    …a penchant for problem-solving and expertise in upstream bioprocessing to join Biologics Process Research & Development (BPR&D) as a Principal Scientist. BPR&D ... and inclusive environment for all. Beyond process development for pipeline biologics , we innovate and build next generation biomanufacturing technologies. Examples… more
    Merck (07/18/25)
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  • Associate Director- QA Compliance

    Gilead Sciences, Inc. (Foster City, CA)
    …audits of Gilead's global suppliers with a primary focus on external biologics manufacturing, contract packaging and contract testing labs. This position will lead ... + Primarily conduct global vendor audits for contract manufacturing of Gilead Biologics + Support and/or conduct audits of providers of raw materials, product… more
    Gilead Sciences, Inc. (06/30/25)
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  • Associate Principal Scientist/Associate Director,…

    Merck (Rahway, NJ)
    …Description** Join Our Team as an Associate Principal Scientist/Associate Director in Biologics Drug Substance Commercialization! Are you ready to make a significant ... of innovation in the Manufacturing Division, specifically within the Biologics Drug Substance Commercialization (BDSC) team. Our Downstream Purification department… more
    Merck (07/24/25)
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  • Director, Pharmaceutical Development

    PCI Pharma Services (Bedford, NH)
    …We are looking for an experienced leader to drive Sterile Pharmaceutical development of Biologics and small molecules, with specific focus on Biologics eg ADCs, ... + Responsible for provision of technical excellence for development projects ( Biologics , small molecules) in line with industry expectations. + To efficiently… more
    PCI Pharma Services (07/24/25)
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  • Director, Microbiology and Sterility Assurance

    Charles River Laboratories (Memphis, TN)
    …not essential, based on experience * Minimum 10 years of experience in a biologics , pharmaceutical, medical device, or related industry. * Minimum 5 years as a ... Certified Quality Engineer (ASQ), desirable * Experience working in a GMP Biologics environment required. * Experience preferred with a CDMO business and/or… more
    Charles River Laboratories (07/23/25)
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