• Senior Process Engineer

    Bristol Myers Squibb (Indianapolis, IN)
    …and execute of assigned projects. . Support commissioning, qualification, and validation activities when applicable . Provide technical support during Startup, PQ ... and validation activities . Support change requests/change control as needed...facility. **Skills and Qualifications** . Experience in the GMP Pharmaceutical or Medical Device industry is required . Experience… more
    Bristol Myers Squibb (09/13/25)
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  • Global Artwork Business Process Owner

    Sanofi Group (Morristown, NJ)
    …creation. This role directly supports Sanofi's ambition to lead the global pharmaceutical industry in digital artwork transformation. We are an innovative global ... Digital to ensure system scalability, data governance, and compliance with validation and cybersecurity standards. **Regulatory & Quality Compliance** + Ensure… more
    Sanofi Group (09/12/25)
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  • Analytical Quality Assurance Specialist

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …well-positioned to successfully emerge as a leading integrated research-based pharmaceutical company. POSITION SUMMARY: The Analytical Quality Assurance (AQA) ... if applicable + Support in the development of methods transfer and validation , troubleshooting, cross validation , IQ/OQ protocols + Document activities with… more
    Glenmark Pharmaceuticals Inc., USA (09/12/25)
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  • Associate Scientist

    Catalent Pharma Solutions (Winchester, KY)
    …work/assist on method development, method transfer, method verification and method validation under appropriate guidance along with routine release and stability ... of client's documents as required including but not limited to specification/ validation reports/test methods/compliance reports etc. to perform gap analysis with… more
    Catalent Pharma Solutions (09/12/25)
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  • Sr. Principal Scientist - TS/MS Device & Packaging

    Lilly (Indianapolis, IN)
    …reports, and other related technical documentation. Oversee qualification and validation strategy for device and packaging processes. + Independently identify ... procedures, deviation investigations, technical reports, change controls, regulatory submissions, validation protocols and summary reports, PFDs, APRs, etc. **Minimum… more
    Lilly (09/12/25)
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  • Automation Manager

    Pfizer (Rocky Mount, NC)
    …such as MS Word, Excel, PowerPoint. + Broad experience in a pharmaceutical environment with a hands-on understanding of control and data acquisition systems, ... Have (Preferred Requirements)** + Prior experience in a high regulated pharmaceutical or biotech manufacturing environment. + Demonstrated experience in project… more
    Pfizer (09/11/25)
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  • Production Maintenance Tech All-Shifts

    Merck (Durham, NC)
    …Technician** Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you! The Sr. ... Maintenance (PM) plans as requested. Responsible for SAP transactions, validation testing support, supporting root cause investigations and change control… more
    Merck (09/10/25)
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  • Tech 3, Utility Maintenance

    Fujifilm (Holly Springs, NC)
    …Practices (cGMP) documentation practices and quality standards in a Pharmaceutical Manufacturing plant. Utilities to include high-pressure steam boilers, process ... accurate maintenance records and documentation * Participates in overseeing validation and qualification activities to ensure compliance with regulatory requirements… more
    Fujifilm (09/09/25)
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  • Senior Scientist, Quality Control

    Amneal Pharmaceuticals (Piscataway, NJ)
    …for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following ... physical and chemical analysis of raw materials, in-process, and finished pharmaceutical products, including products on stability, according to written methods,… more
    Amneal Pharmaceuticals (09/09/25)
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  • Sr. Production Engineer

    Mallinckrodt Pharmaceuticals (Raleigh, NC)
    …operating requirements, process controls, process tolerances, alarm rationalization, and validation . + Prepares periodic reports that summarize production rate, ... problems. 5-10 years of experience in chemical or bulk pharmaceutical (API) manufacturing operations Preferred Skills/Qualifications: Other Skills: Competencies:… more
    Mallinckrodt Pharmaceuticals (09/05/25)
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