• Director, Precision Medicine, Biomarker Lead…

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …Regeneron Genetics Center, Core Facilities, BioAnalysis, etc.) to develop plan for validation and application of research assays **This role may be for you ... Additionally, **10+ years' experience** participating effectively on cross-disciplinary teams in pharmaceutical or biotech industry, including a minimum of **5 years… more
    Regeneron Pharmaceuticals (08/22/25)
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  • Chemist I

    Bausch + Lomb (Greenville, SC)
    …using HPLC/UPLC and GC analytical equipment. Analytical method development, validation and transfer of stability indicating methodologies for actives, related ... and technician level personnel in support of chromatographic testing activities for pharmaceutical , vision care and eye care products. **Key Activities:** + Author… more
    Bausch + Lomb (08/22/25)
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  • Senior Statistical Programmer

    Regeneron Pharmaceuticals (Warren, NJ)
    …datasets utilizing Regeneron tools and methodologies. * Support creation and validation of submission requirements (ie annotated CRF, data export files, define ... experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health related industry. * SAS Certification desirable. EXPERIENCE: *… more
    Regeneron Pharmaceuticals (08/22/25)
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  • Supervisor, Bioanalytical Services

    ICON Clinical Research (Lenexa, KS)
    …planning and execution of bioanalytical studies, including method development, validation , and sample analysis for pharmacokinetics and biomarkers. + Collaborating ... operations, with a strong understanding of regulatory requirements in the pharmaceutical industry. + Strong leadership skills, with experience managing teams and… more
    ICON Clinical Research (08/22/25)
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  • Quality Manager

    WestRock Company (East Flat Rock, NC)
    …procedures. You will support introduction of new equipment on site and validation processes to meet safety and customer expectations. Additionally, you will promote ... * Bachelor\u2019s Degree is preferred, ASQ certification is a plus * Pharmaceutical Printing and / or Packaging industry experience is preferred * Ability… more
    WestRock Company (08/21/25)
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  • Associate Director - Site Systems and Compliance

    Lilly (Lebanon, IN)
    …to drive business process optimization. + Adhere to corporate computer systems validation policies and procedures. + Progress the digital roadmap at the Lilly ... + Minimum of (8) years' experience in manufacturing, preferred in pharmaceutical or other regulated industries. + Experience with integrated business process… more
    Lilly (08/21/25)
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  • Research Scientist II; Analytical Development

    Curia (Albany, NY)
    …Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Analytical Department is responsible for ... * Write analytical method procedures to establish format * Write analytical validation reports * Develop new procedures for new compounds * Process samples… more
    Curia (08/21/25)
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  • Manager, Nonclinical Safety US, Experimental…

    Boehringer Ingelheim (Ridgefield, CT)
    …for all study activities (tissue trimming through archiving), serving as the validation manager for all equipment and software used in the laboratory, as ... expected. + Understanding of toxicology principles and testing programs in the pharmaceutical industry is desirable. + Strict attention to detail and follow-up… more
    Boehringer Ingelheim (08/21/25)
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  • Information Systems, R&D Commercialization…

    Amgen (Washington, DC)
    …platforms and enterprise systems. + Manage UAT planning, test case validation , and production deployment oversight. + Partner closely with cross-functional teams, ... or Agile/Scrum frameworks. + Background in life sciences, biotechnology, or pharmaceutical R&D. + Understanding of the drug development lifecycle and relevant… more
    Amgen (08/21/25)
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  • Sr. Principal MES Advisor - TS/MS - Lebanon API…

    Lilly (Lebanon, IN)
    …skills, complex problem-solving abilities. + Strong knowledge of pharmaceutical manufacturing processes, facility start-up procedures, and GMP regulations. ... + Previous experience supporting cGMP manufacturing within Operations, Validation , Engineering, Technical Services/MSAT, Quality Assurance, etc. + Prior experience… more
    Lilly (08/20/25)
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