• 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 ... Communication skills Project Management + Knowledge in Computer System and Method Validation (Experience preferable) + Strong knowledge and experience with quality … 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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  • 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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  • Sterility Assurance Manager

    ThermoFisher Scientific (Greenville, NC)
    …of aseptic process simulations (media fills). + Experience with pharmaceutical industry technology, especially from a validation , technical or laboratory ... Laboratory or Environmental Monitoring experience, and ideally within a sterile pharmaceutical manufacturing facility). + 5 years of leadership experience required.… more
    ThermoFisher Scientific (07/19/25)
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  • Senior Specialist, Manufacturing Automation

    Merck (West Point, PA)
    …equivalent **Required Experience and Skills:** + Minimum five (5) years in pharmaceutical process automation or equivalent + Experience in Automation Platforms ... is Manufacturing Automation, is responsible for: i) management of all automation process control systems in a live virus vaccine manufacturing facility, ii) leading… more
    Merck (09/10/25)
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  • Quality Associate III, Operations

    Endo International (Cranbury, NJ)
    …clearance to confirm process readiness, non-conforming event support to resolve in- process issues, and process validation and qualification activities. ... QA retains including purging according to retention schedule. + Performs in process validation and equipment qualification activities as required. + Performs… more
    Endo International (08/12/25)
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  • Sr. Principal Manufacturing Scientist - Lebanon…

    Lilly (Lebanon, IN)
    … variability and capability. + Understand, justify and document the state of validation ( process and cleaning) with data that evaluate the capability of ... manufacturing of API molecules. This role will be part of the Manufacturing Process Team for its respective area, providing daily oversight to ensure safe and… more
    Lilly (07/23/25)
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  • Engineer - Automation Engineering - Utilities,…

    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 (08/29/25)
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  • Quality Control Scientist - Microbiology,…

    Catalent Pharma Solutions (Princeton, NJ)
    …safety of products. The position involves routine testing of raw materials, in- process samples, and finished products, as well as environmental monitoring and ... the quality and compliance of raw materials used in pharmaceutical manufacturing. This role involves creating material specifications, conducting identification… more
    Catalent Pharma Solutions (08/19/25)
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  • Senior Sterilization Engineer

    Amgen (Cambridge, MA)
    …The individual will be responsible for designing, conducting, and analyzing new process development, validation and requalification studies for gas sterilization ... dioxide or other gas sterilization modalities + 1+ years in gas sterilization process development, validation and routine production + 1+ years in radiation… more
    Amgen (08/08/25)
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