• Quality Supervisor

    Element Materials Technology (Santa Fe Springs, CA)
    …for overseeing the day-to-day QA operations within a GMP-regulated pharmaceutical environment, ensuring full compliance with applicable regulations, client ... mentorship + Collaborate, review, and approve SOPs, test methods, validation protocols, equipment qualifications, calibrations, verifications, and related documentation… more
    Element Materials Technology (08/23/25)
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  • Director, Quality Operations

    Curia (Albuquerque, NM)
    …Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. Join our talented workforce, where a ... the Director also supports other quality functions, including QSYS, QC, and Validation , during external engagements. This role is central to maintaining compliance,… more
    Curia (08/23/25)
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  • Director - QA Iapi

    Lilly (Indianapolis, IN)
    …supporting the oversight of Insulin or Peptide Purification Active Pharmaceutical Ingredient (API) manufactured within Indianapolis Active Pharmaceutical ... global regulatory manufacturing guidance, and the corporate/industry standards for validation . The position requires working cross-functionally within the site,… more
    Lilly (08/19/25)
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  • Scientist, Analytical R&D

    Amneal Pharmaceuticals (Piscataway, NJ)
    …a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. The individual in this capacity performs ... analytical methods qualifications/validations, analyzes active pharmaceutical ingredients, excipients, and finished dosage forms using appropriate analytical methods… more
    Amneal Pharmaceuticals (08/19/25)
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  • Director- Solid State

    Astrix Technology (Lafayette, IN)
    …Analytical Chemistry!** Join a cutting-edge team driving innovation in pharmaceutical development and preclinical testing. We're seeking an experienced analytical ... product characterization by solid-state analytical techniques. + Oversee method development, validation , and reproduction of prior art. + Manage workload, staffing,… more
    Astrix Technology (08/16/25)
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  • Specialist Quality Control

    Mentor Technical Group (Juncos, PR)
    …MTG has the knowledge and experience to ensure compliance with pharmaceutical , biotechnology, and medical device safety and efficacy guidelines. With offices ... skills Project Management + Knowledge in Computer System and Method Validation (Experience preferable) + Strong knowledge and experience with quality process… more
    Mentor Technical Group (08/16/25)
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  • Regulatory Affairs Associate Director, IVD

    GRAIL (Menlo Park, CA)
    …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... and other stakeholders to support regulatory strategy development, product validation , audits, promotional material review, on-market product support, and change… more
    GRAIL (08/16/25)
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  • Principal Research Scientist I, Analytical…

    AbbVie (North Chicago, IL)
    …for all CMC analytical activities related to the development of AbbVie's pharmaceutical products. Our scope includes AbbVie's diverse pipeline of innovative small ... need experience in analytical control strategies, analytical method development, characterization, validation , release, and stability testing. He/ She should be able… more
    AbbVie (08/15/25)
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  • Equipment & Controls Maintenance Manager

    WuXi AppTec (Middletown, DE)
    …and reliability of base building and manufacturing equipment in our pharmaceutical manufacturing facility. This role is responsible for ensuring all equipment, ... and performance * Oversee the maintenance, repair, and servicing of pharmaceutical manufacturing equipment, automation & controls, clean utilities, and facility… more
    WuXi AppTec (08/13/25)
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  • Business Analyst - Supply Chain Kinaxis Maestro

    Lilly (Indianapolis, IN)
    …end-users and addressing their needs promptly. + Maintain computer system validation for responsible applications. + Deliver recommendations to implement improved ... senior management. **What You Should Bring:** + Deep understanding of pharmaceutical operations, especially in manufacturing, supply chain, and compliance. +… more
    Lilly (08/08/25)
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