• Regional Manager of Southeast CQV Services

    VTI Life Sciences (Raleigh, NC)
    …Relevant, professional experience, ideally within Life Sciences industry, specifically Validation , Commissioning and Qualification within the Pharmaceutical , ... excellence by providing Commissioning, Qualification, Quality Engineering, Automation and Validation Services to the Pharmaceutical , Biotechnology, Biologics and… more
    VTI Life Sciences (06/11/25)
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  • Research Chemist (small molecule mass…

    Intertek (Whitehouse, NJ)
    contract testing, analytical research and development laboratory. Intertek Pharmaceutical Services works directly with both large and small pharmaceutical ... Research Chemist - Mass Spectrometry - Whitehouse, New Jersey Intertek Pharmaceutical Services located in Whitehouse, New Jersey, USA, is a cGMP… more
    Intertek (07/01/25)
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  • Lead Project Engineer, Equipment Commissioning…

    Bristol Myers Squibb (Summit, NJ)
    …strong relationships with other departments. They will also be responsible for managing contract project teams to ensure work is completed on time and in compliance ... to a change management process. + Execute equipment qualifications and validation protocols. + Supervise vendors for qualification functions. + Support development… more
    Bristol Myers Squibb (07/20/25)
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  • CSV Engineer

    Sanofi Group (Swiftwater, PA)
    …Technology fields. + A minimum 4-7 years of relevant experience, preferably in Validation and/or Quality in the pharmaceutical or biotechnology industry. + Key ... our Swiftwater site, supporting directly the manufacturing system automation computer system validation . As a Computerized Systems Validation Engineer, you are… more
    Sanofi Group (07/02/25)
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  • Sr. Principal Manufacturing Scientist - Small…

    Lilly (Lebanon, IN)
    …new molecules. This position will interact with engineering, manufacturing, validation , quality assurance, quality control, development, and regulatory departments. ... Interaction maybe required with other Lilly site/ contract producers of Lilly products. This position requires comprehensive knowledge of the pharmaceutical more
    Lilly (06/07/25)
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  • Automation (Controls) Engineer-Device…

    Lilly (Indianapolis, IN)
    …equipment design. + Tool and Process Validations: Create, execute, and coordinate validation activities with Contract Manufacturers. + Risk Mitigation: Define ... capacity expansions and line extensions for IDM at Lilly sites and Contract Manufacturing receiving sites across the globe. IDM Asset Delivery Automation Engineers… more
    Lilly (07/24/25)
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  • Senior Manager, Contracting Operations - Job ID:

    Ascendis Pharma (Princeton, NJ)
    …their skills. Ascendis Pharma is looking to hire a Senior Manager, Contract Operations to join our team. Responsibilities will include implementing and executing ... implementation of various systems and processes including vendor management, rebate validation , approval of vendor and customer payments, submission of price… more
    Ascendis Pharma (07/08/25)
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  • CSV Systems Engineer III

    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...responsible for supporting Quality Management Systems and Computer System Validation efforts. Additionally, the CSV Systems Engineer III will… more
    Curia (07/23/25)
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  • Senior Manager, Quality Control (Microbiology)…

    Novo Nordisk (Bloomington, IN)
    …6 weeks paid family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition Assistance + Life & Disability Insurance + Employee ... verification + Accountable for completion of qPCR/PCR method development, qualification, validation , and execution + Accountable for daily operations of the site's… more
    Novo Nordisk (04/26/25)
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  • Scientist - Analytical

    Actalent (Sanford, NC)
    …seeking a highly motivated Analytical Scientist to join our Quality Control Method Transfer and Validation team on a 2-year contract . This role is ideal for a ... Job Title: Scientist - Analytical (2-Year Contract ) Schedule: 1st Shift | Monday-Friday, 8:00 AM...assays and manage protocol deviations. + Strong background in pharmaceutical chemistry and analytical method validation . +… more
    Actalent (07/22/25)
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