• Senior Scientist I (Reviewer)

    The US Pharmacopeial Convention (USP) (Rockville, MD)
    …experience in a high-volume pharmaceutical manufacturing QC laboratory or contract pharmaceutical analytical laboratory testing organization is a plus. + ... Scientist I conducts routine and non-routine analyses of raw materials, validation , and stability samples by appropriate analytical methods. The Senior Scientist… more
    The US Pharmacopeial Convention (USP) (07/11/25)
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  • Supervisor, Quality Assurance

    Curia (Hopkinton, MA)
    …where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering ... with pharmaceutical and biotech companies to provide life-saving treatments to...+ Oversee and implement on-floor QA + Review Executed/Unexecuted Validation /Facility Protocols/Reports + Investigate and write documentation for Unplanned… more
    Curia (05/31/25)
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  • Quality Specialist, DI & GxP Systems Compliance

    Catalent Pharma Solutions (St. Petersburg, FL)
    …+ Pharmaceutical and/or life sciences experience including Computer System Validation , 21 CFR Part 11 and general GxP experience preferred. + Demonstrated ... Systems Compliance** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop,… more
    Catalent Pharma Solutions (05/22/25)
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  • Quality Specialist I

    Element Materials Technology (Santa Fe Springs, CA)
    …and work effectively as part of a team + Experience in a pharmaceutical or analytical contract laboratory setting. + Familiarity with electronic quality ... and cGMP. + Participate in QA review of equipment qualification and method validation documentation prepared by technical staff. + Ensure that controlled records are… more
    Element Materials Technology (07/24/25)
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  • Analytical Data Reviewer

    Actalent (East Windsor, NJ)
    …Control and Analytical Development. + Develop and update analytical test reports, validation protocols (IQ/OQ/PQ), and stability study reports. + Prepare method ... validation protocol/reports, method transfer protocol/reports, and technical documents including change controls, deviations, CAPAs, and OOS investigations. + Ensure… more
    Actalent (07/18/25)
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  • Microbiologist I

    Curia (Albuquerque, NM)
    …where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering ... with pharmaceutical and biotech companies to provide life-saving treatments to...procedures and regulatory requirements. + Assist in the qualification, validation , and calibration of microbiology laboratory instruments and test… more
    Curia (06/21/25)
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  • Manager, Quality Assurance Operations

    Cambrex High Point (Longmont, CO)
    …Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development ... drug product. * Experienced with review and approval of equipment and instrument validation as well as associated computer software validation . * Provide… more
    Cambrex High Point (06/20/25)
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  • Associate Director, Commercial Quality Assurance

    Catalent Pharma Solutions (Greenville, NC)
    …Quality Assurance** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... all commercial manufacturing and laboratory operations onsite and at contract organizations (CMOs and CPOs). **The Role** + Act...at least 7 years of professional experience in QA/QC pharmaceutical manufacturing or; + Master's degree with at least… more
    Catalent Pharma Solutions (06/03/25)
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  • Associate Scientist II, Quality Control

    Catalent Pharma Solutions (St. Petersburg, FL)
    …II, Quality Control** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... captive zone environmental analysis, as well as cleaning and process validation support. The department provides analytical services to manufacturing, Technical… more
    Catalent Pharma Solutions (07/22/25)
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  • Quality Engineer

    US Tech Solutions (Durham, NC)
    **Duration: 12-month contract ** **Job Description:** + Provide product team support including, Material Review Board (MRB), customer complaint activities, ... statistical analysis, validation support, inspection plans, metrology, quality metrics and report...a regulated industry such as health care, medical device, pharmaceutical , etc). **Skills:** + Good understanding of Continuous Improvement… more
    US Tech Solutions (07/18/25)
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