• Lead Project Manager- CMO Tech Transfers

    GE HealthCare (Arlington Heights, IL)
    …and MSAT teams to ensure robust transfer packages. + Support scale-up activities, process validation , and readiness for commercial production. + **Risk & ... & supply chain network in USCAN. This role ensures successful scale-up, validation , and commercial readiness of drug products while maintaining compliance with… more
    GE HealthCare (01/10/26)
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  • Associate Director - Joint Process Team

    Lilly (Indianapolis, IN)
    Process Research & Development group on commercialization (technology transfer, process validation and regulatory approval) of Lilly's exciting leading ... through philanthropy and volunteerism. **Outline of Role:** Associate Director, Joint Process Team (JPT) is responsible for leading a cross functional team… more
    Lilly (12/18/25)
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  • Senior Process Development Engineer

    Abbott (St. Paul, MN)
    …medicines. Our 114,000 colleagues serve people in more than 160 countries. Senior Process Development Engineer **Working at Abbott** At Abbott, you can do work that ... is seeking a high caliber, motivated, self-driven leader to join our Process Development engineering team for delivery catheter system development in Abbott's… more
    Abbott (11/02/25)
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  • Quality Compliance & Systems Manager

    Insight Global (Midlothian, VA)
    …support the review and approval of all GxP IT system change controls and validation documents, manage the product quality complaints process , and support the ... quality experience, in a regulated industry such as FDA regulated and pharmaceutical - Experience supporting computer system validation (CSV) activities across… more
    Insight Global (01/09/26)
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  • GXP Systems Analyst, Operational Technology

    United Therapeutics (Silver Spring, MD)
    …are as follows:** **Who We Are** We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public ... brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of...a strong attention detail and managing the change control process is second nature to you. The GxP Systems… more
    United Therapeutics (12/11/25)
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  • Clinical Systems Quality Manager - Hybrid

    Merck (North Wales, PA)
    …Project Lifecycle, IT Systems Development, Leadership, Leadership Mentoring, Management Process , Pharmaceutical Regulatory Affairs, Quality Assurance Processes, ... and the User Community to provide quality services associated with the validation and compliance of automated computer systems (eg Change Control, Doc. Management,… more
    Merck (01/14/26)
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  • Process Mechanic 2

    Fujifilm (Research Triangle Park, NC)
    …eliminate future breakdowns + Supports project engineering with design, installation, and validation of new plant systems, including facility, process , lab, and ... **Position Overview** The Process Mechanic 2 is responsible to perform general...Additionally, this role ensures systems meet stringent requirements of pharmaceutical manufacturing. **Company Overview** At FUJIFILM Biotechnologies, we're leading… more
    Fujifilm (12/16/25)
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  • QC Data Reviewer

    Actalent (Mount Prospect, IL)
    …and assisting in audits and investigations related to testing deviations for pharmaceutical products. You will play a critical role in ensuring quality control ... + Oversee testing conducted by chemists on finished products, raw materials, in- process samples, components, and stability study samples. + Perform testing of new… more
    Actalent (01/17/26)
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  • Director, Analytical Chemistry - Antibody-Drug…

    Lilly (Indianapolis, IN)
    …Located in Indianapolis, IN, scientists have full access to Lilly's deep pharmaceutical development expertise and engineering capabilities. In this role, we are ... apply their strong foundation in analytical sciences and experience in pharmaceutical development to enable clinical trials, regulatory submissions, and new product… more
    Lilly (12/15/25)
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  • IDAP Engineer - MES Systems

    Lilly (Indianapolis, IN)
    …assembly or packaging operations. + Working knowledge of cGMP and Computer System Validation (CSV) frameworks + Ability to interpret process requirements and ... and validation . + 3+ years of experience in regulated pharmaceutical or medical device manufacturing environments. **Additional Preferences:** + Familiarity with… more
    Lilly (01/09/26)
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