• Director of Quality - BioAnalytical

    Catalent Pharma Solutions (Kansas City, MO)
    …support and work with customers to resolve quality concerns as appropriate. The Quality Director is the business partner to Operations and advisor to the ... ** Director , Quality , BioAnalytical** Catalent, Inc. is...objectives and focused on ensuring specific focus upon best-in-class Quality Control related procedures; + Maintain an… more
    Catalent Pharma Solutions (11/11/25)
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  • QA Director - Site Investigations…

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    QA Director - Site Investigations & Quality systems Department: Quality Plant Head Location: Monroe, NC START YOUR APPLICATION ... with Regulatory requirements. Under the direction of the Senior Director of Quality , this position is also...but is not limited to, the following systems: Document Control , Electronic Quality Management Systems (Investigation, Change… more
    Glenmark Pharmaceuticals Inc., USA (10/06/25)
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  • Director , Quality

    Catalent Pharma Solutions (Kansas City, MO)
    Quality approval of specifications, sampling instructions, test methods and other Quality Control procedures. + Other duties as assigned. **The Candidate** + ... ** Director , Quality ** **Position Summary** Catalent, Inc....industry with increasing levels of responsibility and leadership in quality assurance, compliance and quality control more
    Catalent Pharma Solutions (10/10/25)
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  • Director of Quality

    Catalent Pharma Solutions (Chelsea, MA)
    Director of Quality Catalent, Inc. is a...function including Quality Assurance, Quality Control and batch release within a pharmaceutical GMP ... Department - Quality Assurance and Laboratory (Analytical Development/ Quality Control ). The responsibility of the role...member of the site leadership team ensure an effective Pharmaceutical Quality Management system is in place,… more
    Catalent Pharma Solutions (11/11/25)
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  • Senior Director - Quality Assurance…

    Gilead Sciences, Inc. (Foster City, CA)
    …Qualifications:** + 12+ years' experience in Biopharmaceutical or Pharmaceutical manufacturing quality assurance and quality control . Stays ahead of ... and help create possible, together. **Job Description** The Senior Director , Quality Assurance leads the site's independent...Leadership & Strategy** + Demonstrate ownership of a **site Pharmaceutical Quality System (PQS)** aligned to our… more
    Gilead Sciences, Inc. (11/14/25)
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  • Associate Director - Quality

    Lilly (Indianapolis, IN)
    …manufacturing environment in any of the following associated disciplines: TSMS, Production, Quality Assurance, Quality Control , Engineering, or Regulatory ... life better for people around the world. #WeAreLilly **Responsibilities:** The Associate Director - Quality Assurance (QA) API External Manufacturing is… more
    Lilly (10/30/25)
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  • Sr. Director - Quality - Small…

    Lilly (Indianapolis, IN)
    …Small Molecules, Large Molecule and Peptide APIs at external manufacturing facilities globally. The Sr. Director - Quality - Small Molecule API EM is the Site ... and cGMPs and drive continuous improvement to adapt to the business requirements. The Sr. Director - Quality - Small Molecule API EM is responsible to stay… more
    Lilly (10/30/25)
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  • Associate Director Plant Quality

    BD (Becton, Dickinson and Company) (Sandy, UT)
    **Job Description Summary** Reporting to the VP Quality Management, the Associate Director Plant QA provides direct management to technical and managerial staff ... effective problem solving and active management of ambiguous situations; Associate Director ensures product safety, product quality and compliance with… more
    BD (Becton, Dickinson and Company) (11/13/25)
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  • Associate Director , Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring the ... revised regulations and impact. + Ensure implementation of change control and actions completed to address new and revised...with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development,… more
    Takeda Pharmaceuticals (11/14/25)
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  • Program & Technical Advisor (Sr.…

    Guidehouse (Mclean, VA)
    …CDISC data standards + Experience in pharmaceutical industry regulatory affairs and/or quality assurance and/or quality control + Direct experience in ... advance services including but not limited to data cleaning, data transfers, data quality control , data integration and validation, data analysis and report… more
    Guidehouse (11/09/25)
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