• Automation/Senior Automation Engineer

    Genentech (Hillsboro, OR)
    …have the opportunity to collaborate closely with key stakeholders in Process Development, Analytical Development, Manufacturing, and Quality. **The Opportunity:** As ... gene therapy manufacturing processes. + Partner with stakeholders, including Process Development, Analytical Development, Manufacturing, and Quality teams, to… more
    Genentech (11/11/25)
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  • Staff Engineer, Chemical Manufacturing

    Terumo Neuro (Aliso Viejo, CA)
    … process modifications, clarify problems, and develop processes. + Manage process validation and product transfer activities across different manufacturing ... (eg, MP, Routers, BOM, etc.). + Draft and execute validation of chemistry product, equipment, and processes. + Lead...etc.). + Identify and execute improvements, issues, or any process requirement with minimum supervision. + Comply with applicable… more
    Terumo Neuro (11/05/25)
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  • Staff Packaging & Assembly Engineer

    ThermoFisher Scientific (Greenville, NC)
    …with vendors. The ideal candidate will have a strong background in pharmaceutical engineering, process improvements, and experience with Factory Acceptance Tests ... the creation and maintenance of product Design Master Records (DMRs) post-submission ** Process Improvement:** + Identify and implement process improvements to… more
    ThermoFisher Scientific (12/06/25)
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  • Engineer - Automation Engineering - Historian…

    Lilly (Lebanon, IN)
    …support for one or more operating areas across site and/or for capital projects. Process Automation is core to delivering a right first time facility start up and ... a key technical expert with partners to influence and implement within the process control organization and across functional disciplines to support the process … more
    Lilly (12/27/25)
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  • Quality Manager

    Mitsubishi Chemical Group (Wilmington, MA)
    …product and raw material release, batch record review, investigations, audits, CAPA, validation , and training. This position also serves as the ISO Management ... ensuring audit readiness and certification compliance + Support qualification and validation activities for processes, equipment, and systems + Design and implement… more
    Mitsubishi Chemical Group (12/23/25)
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  • Senior Automation Project Engineer

    Reckitt (Zeeland, MI)
    …of automation projects + Leads stakeholders throughout automation lifecycle process including identification of system user requirements, design of systems, ... and commissioning and validation of systems + Manages scope, schedule, and budget...control systems in a consumer-packaged goods, infant formula, or pharmaceutical manufacturing environment + Requires experience with manufacturing control… more
    Reckitt (12/12/25)
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  • Software Quality Engineer II

    Abbott (Sylmar, CA)
    …and training to the site engineers for Non-Product Software development and validation , Data Integrity, Cybersecurity, 21 CFR part 11 requirements and ensure ... Engineering in the completion of system/software requirements and other verification and validation processes. + Create and execute or direct software validation … more
    Abbott (11/18/25)
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  • Quality Engineer II / Sr Quality Engineer

    BD (Becton, Dickinson and Company) (Sparks, MD)
    …and identifies/recommends opportunities for continuous improvement (internal/external). Responsibility for process validation across all media plants. Moderate ... with us. **Responsibilities:** + Required experience in independently writing and executing process validation protocols. + Experience in a medical device or… more
    BD (Becton, Dickinson and Company) (10/30/25)
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  • Bioprocess Technician IV

    Pfizer (Sanford, NC)
    …Supports operation of manufacturing equipment and issue resolution associated with process equipment commissioning, qualification and validation . + Drives ... Points If You Have** **(Preferred Requirements)** + Experience in a pharmaceutical manufacturing environment + Knowledge of process improvement methodologies… more
    Pfizer (01/18/26)
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  • TSMS Sterility Assurance Scientist

    Lilly (Pleasant Prairie, WI)
    … validation , technical services, and/or quality assurance associated cGMP pharmaceutical manufacturing. + 2+ years in pharmaceutical manufacturing preferred ... guidance and expertise in environmental monitoring, contamination control, aseptic process simulations, gowning/aseptic techniques, and cleaning/sanitization strategies, including disinfectant… more
    Lilly (01/13/26)
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