• QA Auditor

    IQVIA (Durham, NC)
    US Homebased **Job Description** Provide global regulatory oversight of validation management as part of the Quality Management System. This oversight includes ... and procedure related to GxP compliance, guidance, audit support, review of validation deliverables, and approving release for use as related to Laboratory System… more
    IQVIA (01/09/26)
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  • CQV Engineer

    VTI Life Sciences (San Francisco, CA)
    …excellence by providing Commissioning, Qualification, Quality Engineering, Automation and Validation Services to the Pharmaceutical , Biotechnology, Biologics and ... and ambitious engineers looking to accelerate their career in the pharmaceutical , biotechnology and medical device industries. We offer an opportunity to… more
    VTI Life Sciences (12/13/25)
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  • Automation Engineer

    VTI Life Sciences (San Francisco, CA)
    …excellence by providing Commissioning, Qualification, Quality Engineering, Automation and Validation Services to the Pharmaceutical , Biotechnology, Biologics and ... and ambitious engineers looking to accelerate their career in the pharmaceutical , biotechnology and medical device industries. We offer an opportunity to… more
    VTI Life Sciences (12/13/25)
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  • Lead Process Scientist, Drug Product (Sr.…

    Takeda Pharmaceuticals (Brooklyn Park, MN)
    …Technology transfer to internal sites and external contract manufacturing organizations (CMOs) + Process validation planning and execution support + Process ... By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application… more
    Takeda Pharmaceuticals (12/24/25)
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  • Chemical Process Engineer

    Endo International (Raleigh, NC)
    …Skills/Qualifications:_ _Other Skills:_ _Competencies:_ Understanding of GMPs (ICH Q7) and process validation Understanding of Six Sigma and Lean Manufacturing ... Activities include project scoping, operating requirements, process controls, process tolerances, alarm rationalization, and validation . + Prepares periodic… more
    Endo International (11/12/25)
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  • Process Development Senior Scientist

    Amgen (Thousand Oaks, CA)
    …Analytical Chemistry, Biochemistry, Biochemical or Chemical Engineering + 3+ years pharmaceutical /biotech experience in process development and analytical method ... Join us and transform the lives of patients while transforming your career. ** Process Development Senior Scientist** **What you will do** Let's do this. Let's change… more
    Amgen (11/20/25)
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  • Senior Sterilization Engineer (Expert, Multiple…

    Eurofins US Network (Lancaster, PA)
    …+ **Minimum 7-10+ years** in sterilization engineering or sterile product validation , ideally within medical device or pharmaceutical industries. + ... of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract...gamma/X‑ray, or VHP + steam) with hands-on experience in process development and validation . + In‑depth knowledge… more
    Eurofins US Network (12/30/25)
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  • Electro-Mechanical Technician

    Kelly Services (Blue Ash, OH)
    …basic engineering and statistical techniques, including process capability studies, validation protocols, and process validation activities. + Develop ... Experience supporting FDA-regulated or ISO-compliant environments. + Familiarity with process validation , equipment qualification, and component qualification… more
    Kelly Services (01/13/26)
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  • Associate Process Engineer (Cleaning…

    Novo Nordisk (West Lebanon, NH)
    …+ 14 weeks Paid Parental Leave + Free access to Novo Nordisk-marketed pharmaceutical products At Novo Nordisk, you will find opportunities, resources and mentorship ... you ready to realize your potential? The Position A process engineer on the cleaning team is a ...who specializes in the cleaning and sterilization of GMP pharmaceutical manufacturing equipment in line with Novo Nordisk and… more
    Novo Nordisk (11/05/25)
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  • Manager, CSV - Equipment and Instrumentation

    Bristol Myers Squibb (Summit, NJ)
    …qualification and support requests. + Provides technical support and guidance on Validation , Quality Process , and equipment qualification issues. Interfaces with ... documentation practices relating to systems, equipment, and instrumentation within the pharmaceutical industry. + Strong working knowledge of ISPE guidance, 21 CFR… more
    Bristol Myers Squibb (01/12/26)
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