• Medical Device Manufacturing

    Eurofins (Indianapolis, IN)
    …well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised ... all activities follow established safety standards, regulatory requirements and Good Manufacturing Procedures (GMP) + Lead team, schedule, and train employees in… more
    Eurofins (05/13/25)
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  • Asset Delivery C&Q Process Owner - IDM

    Lilly (Indianapolis, IN)
    …and handle complex tasks. + Previous involvement in IDM's C&Q Process, previous medical device manufacturing industry experience, and experience working ... life better for people around the world. The Indy Device Manufacturing (IDM) Process Engineering Group...Skills/Preferences:** + Previous involvement in IDM's C&Q Process, previous medical device manufacturing industry experience,… more
    Lilly (06/21/25)
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  • Specialist, Document Disclosure

    Merck (Indianapolis, IN)
    **Job Description** The Medical Writing & Disclosure Department of the GCTO organization prepares a variety of regulated documentation in support of the clinical ... with external researchers. The Specialist provides support to document disclosure group and holds primary responsibility for ensuring the company's compliance with… more
    Merck (06/25/25)
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  • Sr. Specialist, Quality Assurance

    Cardinal Health (Indianapolis, IN)
    …with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device ) preferred + Possess an understanding of cGMP/compliance requirements for ... Environment_** + The primary work environment consists of a radiopharmaceutical manufacturing facility. + Employees may handle radioactive materials and may be… more
    Cardinal Health (06/20/25)
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