• 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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  • Senior Systems Engineer

    Teledyne (Thousand Oaks, CA)
    …research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals who thrive on making an ... product requirements, lead trade studies, and guide integration, verification, and validation efforts. You'll contribute to both R&D initiatives and the evolution… more
    Teledyne (09/03/25)
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  • QC Microbiologist 1

    GE HealthCare (Arlington Heights, IL)
    …and supports validation studies as they pertain to microbiology. Our Pharmaceutical Diagnostics (PDx) business is a global leader in imaging agents, used to ... is responsible for in-process and release testing of injectable pharmaceutical finished products. The role includes final product microbiological testing,… more
    GE HealthCare (09/03/25)
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  • Sr. Director Analytical GMP Laboratories - Lilly…

    Lilly (Lebanon, IN)
    …strategies for meeting regulatory agency requirements as pertains to analytical method validation and testing. + Drives continuous improvement of systems within the ... documents consistent with procedure requirements; including but not limited to, validation packages, suspect result reviews, deviations and change controls as… more
    Lilly (08/30/25)
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  • Senior Analyst, QC Biochemistry

    BeOne Medicines (Pennington, NJ)
    …GMP audits, as needed. + Participate in transfer and method validation activities, including protocol preparation, protocol execution, and report preparation. + ... and cGMP/EU GMP regulations. + Familiar with instrument and equipment validation . + Impressive, demonstrable track record and skills/experience gained within a… more
    BeOne Medicines (08/29/25)
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  • Global Translational Medicine Lead

    Astellas Pharma (Northbrook, IL)
    …of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We ... relevant experience in drug discovery and clinical development in a biotech/ pharmaceutical company, particularly with experience in the identification and … more
    Astellas Pharma (08/29/25)
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  • Principal Controls and Automation Engineer

    Bausch + Lomb (Greenville, SC)
    …leadership of Engineering projects and Project Management for new pharmaceutical and lens care manufacturing platforms and infrastructure, products, processes ... ensure successful applications development and integration activities through manufacturing validation to established acceptance criteria. + Provide technical and… more
    Bausch + Lomb (08/27/25)
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  • Senior Chemist, Nuclear Manufacturing (Material…

    Cardinal Health (Beltsville, MD)
    …analytical equipment configuration, document creation and technical review, executing method validation , and process qualification, as well as production and testing ... activities typical for a cGMP pharmaceutical manufacturing operation including but not limited to the preparation of chemicals and components, the operation of… more
    Cardinal Health (08/21/25)
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