• Scientist / Sr. Scientist, Analytical Development

    Cambrex High Point (Waltham, MA)
    …compendial testing. Qualifications/Skills + Proven experience in method development, validation , troubleshooting, and transfer for pharmaceutical synthetic ... a PhD with 1+ years of experience in analytical chemistry within the pharmaceutical industry. The candidate should have a broad experience of method development of… more
    Cambrex High Point (08/14/25)
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  • IT Business Process Analyst III

    Teva Pharmaceuticals (West Chester, PA)
    …troubleshooting, and administration of new and existing systems within the pharmaceutical laboratory research and development organization. * Support delivery of IT ... new releases, upgrades and changes in accordance with Computer Systems Validation (CSV) standards. * Perform day-to-day system administration, maintenance &… more
    Teva Pharmaceuticals (07/24/25)
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  • Quality Assurance Engineer

    Danaher Corporation (Muskegon, MI)
    …The Quality Assurance Engineer will be the subject matter expert for the validation strategy and maintain ownership of the Muskegon site Validation Master ... Qualification (IQ), Operation Qualification (OQ), Performance Qualification (PQ), process validation (PV), cleaning validation (CV) and Computer Software… more
    Danaher Corporation (09/05/25)
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  • Design Quality Engineer

    Bio-Techne (Wallingford, CT)
    …**Position Summary:** The Design Quality Engineer supports the qualification and validation of new products and product modifications, new equipment builds and ... ISO standards during design & development and verification & validation activities. This position closely collaborates with the Engineering, Manufacturing,… more
    Bio-Techne (08/28/25)
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  • CVS Engineering Support Tech (Part-Time)

    Fujifilm (College Station, TX)
    **Position Overview** The Computer System Validation (CSV) Engineering Support Tech will support cross-functional teams by assisting in drafting and executing ... validation protocols for computer systems and process control systems....chemical Engineering or equivalent. . Interest in biotechnology or pharmaceutical systems. . Willingness to learn and adapt in… more
    Fujifilm (08/26/25)
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  • Res Qual Assur Coord IV

    University of Rochester (Rochester, NY)
    …ClinPro by acting as second QA check of the execution of validation scripts, and manages metrology activities; calibration of in-process packaging equipment and ... Technical Writing + Write new and update existing SOP's as needed. Author validation protocols as necessary for new and existing equipment. + Set-up QA metrology… more
    University of Rochester (08/09/25)
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  • Clinical Lead, Early Clinical and Experimental…

    Sanofi Group (Morristown, NJ)
    …Proof-of-Mechanism/Proof-of-Concept, as well as natural history studies and experimental model validation to contribute building the Human Target Validation ... of multiple disciplines into a coherent translational medicine and human target validation plan is essential. We are an innovative global healthcare company with… more
    Sanofi Group (07/29/25)
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  • Vice President of Commissioning, Qualification…

    Fujifilm (Durham, NC)
    …The role will serve as the system owner for FDB's electronic validation lifecycle management system. The Vice President of Commissioning, Qualification and Ops ... with Engineering, Quality Assurance, and Operations teams to integrate validation processes into project workflows, ensuring seamless execution and compliance.… more
    Fujifilm (06/19/25)
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  • Analytical Chemistry Scientist

    Hovione (East Windsor, NJ)
    …as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market. Our people ... to ensure that the timelines of the analytical work (such as method development, validation protocols, validation execution, and validation reports) of the… more
    Hovione (09/07/25)
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  • Commissioning & Qualification Program Lead

    Genentech (Holly Springs, NC)
    …in the project. + Develop C&Q execution strategies in alignment with Pharmaceutical Quality Management System, global standards and processes and regulations. + ... related discipline with 20 or more years of experience preferable in pharmaceutical /biopharmaceutical industry. + Experience in management of C&Q scope in capital… more
    Genentech (09/06/25)
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