• Construction Project and Program Manager

    Caris Life Sciences (Phoenix, AZ)
    …and protocols. + Deliver required documentation for Construction Qualifications, Validation , and protocols. Stakeholder Engagement + Serve as the primary ... and mitigate risks across the program portfolio. + Ensure quality standards and validation requirements are met for all facilities. + High degree of safety… more
    Caris Life Sciences (12/10/25)
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  • Statistical Analyst - (ADaM / TLF) Hybrid

    AbbVie (South San Francisco, CA)
    …Analyst is an integral role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and ... for the creation of Tables, Listings and Figures. + Validation of ADaM data sets. Validation of...CDISC Standards. + Basic understanding of the drug development process . + Ability to communicate clearly both oral and… more
    AbbVie (12/06/25)
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  • Manager, Quality Control Physicochemistry

    BeOne Medicines (Pennington, NJ)
    …Physicochemistry laboratory routine operations, including but not limited to validation , SOPs, specifications, testing records, personnel training and assessment, ... Health and Safety (EHS) standards. + Ensure timely completion of testing (eg, In- process control, DS release, DP release, and stability testing) to ensure timely… more
    BeOne Medicines (12/05/25)
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  • Jt241 - Microbiologist Steriliz I

    Quality Consulting Group (Juncos, PR)
    QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... + Analyzes chemical, biological or microbiological products, raw materials, in- process materials, release test samples or stability samples in support… more
    Quality Consulting Group (12/04/25)
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  • Senior Compliance & CQV Engineer

    Hovione (East Windsor, NJ)
    …design, implementation, and qualification (mandatory) + Experience in chemical or pharmaceutical industry preferred + Strong understanding of validation , ... standards and project requirements. + Drive effective coordination between engineering, validation , manufacturing, QA, and IT functions during project delivery. +… more
    Hovione (12/03/25)
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  • Discovery Lead - Women's Health & Musculoskeletal…

    Lilly (Boston, MA)
    …and mentor PhD and non-PhD scientists engaged in target identification, validation and preclinical drug discovery + Supervise laboratories. Ensure adherence to ... for novel small and large molecule target discovery and validation + Coach team members to think deeply and...10 years of experience in drug discovery in the pharmaceutical industry. + Thorough understanding of drug discovery and… more
    Lilly (11/26/25)
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  • Pharmacometrics Analyst (SAS Programming)

    AbbVie (North Chicago, IL)
    …Analyst is an integral role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and ... for the creation of Tables, Listings and Figures. + Validation of ADaM data sets. + Validation ...CDISC Standards. + Basic understanding of the drug development process . + Ability to communicate clearly both oral and… more
    AbbVie (11/20/25)
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  • Research Analyst III, Bioanalytical Chemistry…

    Charles River Laboratories (Cleveland, OH)
    …studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and ... write both study and non-study deviations + Independently participate in process improvement initiatives as needed + Develop and maintain critical thinking,… more
    Charles River Laboratories (11/16/25)
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  • Quality Control (QC) Microbiology Manager

    Reckitt (Salt Lake City, UT)
    …day to day execution of microbiological testing of raw materials, in- process samples, finished products and Environmental Monitoring samples in conformance with ... / qualified to appropriate standards. + Create and maintain SOPs, protocols, and validation documents and lead investigations into OOS/OOT and CAPA's. + All other… more
    Reckitt (11/06/25)
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  • Sr. IT Program Manager

    ThermoFisher Scientific (Waltham, MA)
    …Compliance & Inspection Readiness** + Ensure all IT programs meet global regulatory and validation standards (21 CFR Part 11, GxP, GAMP 5, EU Annex 11). + Maintain ... ongoing inspection readiness by ensuring complete validation documentation and traceability. + Partner with Quality and Compliance teams to prepare for internal and… more
    ThermoFisher Scientific (10/31/25)
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