• Automation Engineer III

    Catalent Pharma Solutions (Chelsea, MA)
    …control systems (Siemens, Schneider, etc.) is preferred + Requires knowledge of: pharmaceutical process equipment and Clean In Place (CIP) systems, ANSI/ISA-88 ... senior engineering staff. The candidate takes ownership of automation engineering, design, validation , and the implementation of new control systems to achieve cost… more
    Catalent Pharma Solutions (01/07/26)
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  • Automation Engineer II

    Catalent Pharma Solutions (Chelsea, MA)
    …control systems (Siemens, Schneider, etc.) is preferred + Requires knowledge of: pharmaceutical process equipment and Clean In Place (CIP) systems, ANSI/ISA-88 ... manufacturing. The candidate provides support in automation engineering, design, and validation . The Automation Engineer II contributes to the design and… more
    Catalent Pharma Solutions (01/01/26)
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  • Manufacturing Engineer

    Actalent (Petersburg, VA)
    …seeking a highly skilled and experienced Manufacturing Engineer to join our pharmaceutical manufacturing plant. The ideal candidate will be responsible for the ... regulatory standards. This role requires a deep understanding of pharmaceutical manufacturing processes, equipment, and GMP (Good Manufacturing Practices)… more
    Actalent (01/14/26)
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  • Operations Manager - Night Shift

    Lilly (Concord, NC)
    …+ Facility, Equipment, Systems Start-up + Equipment design, qualification, and process validation . + Manufacturing Execution Systems and electronic batch ... the project phase, the Operations Manager (OM) will support commissioning, qualification, and validation of the Device Assembly and Packaging (DAP) areas as well as… more
    Lilly (01/13/26)
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  • Instrumentation Technician

    PACIV (Indianapolis, IN)
    PACIV stands for Process Automation, Controls, Instrumentation, and Validation . At PACIV, we are passionate about delivering world-class automation & ... validation solutions that empower many industries and advanced manufacturing....process instrumentation for capital projects, particularly within the pharmaceutical sector. Managing all aspects of instrumentation logistics, procurement,… more
    PACIV (01/10/26)
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  • Sr Associate Scientist I - Microbiology

    Bristol Myers Squibb (Indianapolis, IN)
    …role will also involve advanced laboratory analyses, troubleshooting efforts, method validation and qualifications ensuring compliance with regulatory and QA system ... and media qualification testing. + Execute method qualification, verification and validation studies with minimal supervision. + Troubleshoot assay related issues… more
    Bristol Myers Squibb (01/07/26)
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  • Associate Director - TSMS Sterility Assurance

    Lilly (Pleasant Prairie, WI)
    …relates to drug product manufacturing, specifically the formulation/filling/inspection of pharmaceutical products. The Associate Director will provide guidance on ... procedures, deviation investigations, technical reports, change controls, regulatory submissions, validation protocols and summary reports, PFDs, APRs, etc. + Define… more
    Lilly (01/01/26)
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  • Quality Control Environment Monitoring Supervisor

    Bristol Myers Squibb (Indianapolis, IN)
    …manner. + Approval of SOPs, trend data, investigations, non-conformances, validation protocols, reports, validation /verifications and equipment qualifications. + ... EM technologies and improve data visibility. + Identify other opportunities for process improvements and implement changes to increase quality and efficiency within… more
    Bristol Myers Squibb (12/23/25)
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  • QC Chemist I

    GE HealthCare (Arlington Heights, IL)
    **Job Description Summary** You will be responsible for in- process and release testing of Injectable pharmaceutical finished products produced on site. The ... Participates in validation projects requiring analytical support. + Contributes to process improvement through Lean and 5S. + Assists in the stocking and… more
    GE HealthCare (12/05/25)
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  • Associate Director - TS/MS Peptides

    Lilly (Indianapolis, IN)
    …a fast-paced, dynamic, and highly collaborative environment. + Experience with process validation , technology transfer, and regulatory filings (IND/NDA/BLA) is ... robust and compliant manufacturing of peptide drug substances, from process development through commercialization and life cycle management. **Job Responsibilities**… more
    Lilly (11/13/25)
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