• Senior Validation Specialist I, BioAnalytics…

    Catalent Pharma Solutions (Kansas City, MO)
    **Senior Validation Specialist I, BioAnalytics Computer System Validation ( CSV ) & Compliance** **Position Summary:** Catalent, Inc. is a leading global contract ... City, MO (KCM) is hiring a Senior Validation Specialist I, BioAnalytics CSV & Compliance. The Senior Validation Specialist is primarily responsible for leading,… more
    Catalent Pharma Solutions (08/22/25)
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  • CSV Specialist/Engineer IT Systems

    PACIV (San Juan, PR)
    …the Life Sciences sector, is looking for a Computerized System Validation ( CSV ) Specialist/Engineer IT Systems , for its Puerto Rico office. Job Description: ... The Computerized System Validation ( CSV ) Specialist/Engineer will be responsible for development and execution of Computerized System Validation ( CSV )… more
    PACIV (07/13/25)
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  • CSV Engineer

    Sanofi Group (Swiftwater, PA)
    **Job Title:** CSV Engineer **Location:** Swiftwater, PA **About the Job** We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless ... Engineer will be responsible for ensuring all Computerized Systems Validation ( CSV ) lifecycle activities meet Sanofi's quality requirements and fulfil regulatory… more
    Sanofi Group (07/02/25)
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  • Sr. IT Engineer 1, CSV

    Fujifilm (Holly Springs, NC)
    **Position Overview** The Sr. IT Engineer 1, CSV is the Subject Matter Expert (SME) and leads tasks associated with Computer System Validation ( CSV ). This role ... https://www.fujifilm.com/us/en/about/region/careers **Job Description** **What You'll Do** + Ensures that CSV is conducted in a consistently high standard, within… more
    Fujifilm (08/11/25)
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  • CSV Systems Engineer III

    Curia (Albuquerque, NM)
    CSV Systems Engineer III in Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract development and ... Quality Management Systems and Computer System Validation efforts. Additionally, the CSV Systems Engineer III will provide guidance and expertise on various… more
    Curia (07/23/25)
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  • CSV Automation Engineer

    J&J Family of Companies (Wilson, NC)
    …internal/external network. Apply today for this great opportunity located in Wilson, NC! The CSV Automation Engineer works with the CSV Automation Lead and is ... lifecycle, ensuring compliance with regulatory requirements, Computer Systems Validation ( CSV ) and Lifecycle procedures with Data Integrity requirements. The… more
    J&J Family of Companies (08/26/25)
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  • Sr. Manager of Enterprise Quality CSV

    J&J Family of Companies (Raritan, NJ)
    …are searching for the best talent for a **Sr. Manager of Enterprise Quality CSV ** to be located in Raritan, NJ and/or Horsham, PA. **Purpose:** Enterprise Quality ... J&J's Systems Development Life Cycle (SDLC) and Computer System Validation ( CSV ) Framework, assuring compliance across the enterprise with applicable global… more
    J&J Family of Companies (08/27/25)
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  • Lead Engineer, CSV

    Bristol Myers Squibb (Summit, NJ)
    …with our Cell Therapy team. The **Lead Computer System Validation ( CSV ) Engineer** supports the successful implementation of manufacturing and laboratory equipment ... all lifecycle deliverables in the Qualification of equipment and full CSV for single and multi-user Computerized Systems. + Develops validation/qualification… more
    Bristol Myers Squibb (08/30/25)
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  • CSV Specialist I

    Charles River Laboratories (Memphis, TN)
    …vendors, etc). * Provide guidance and support on Computer System Validation ( CSV ) practices, helping others develop skills and knowledge in regulatory compliance, ... Certified Quality Auditor (CQA), Certified Quality Engineer (CQE), or specialized CSV training can be advantageous. * Other: Comprehensive knowledge of regulatory… more
    Charles River Laboratories (08/19/25)
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  • CSV Technical Writer

    Capgemini (Titusville, NJ)
    **About the job:** Technical Writing and CSV for the pharma industry **What you will do at Sogeti:** + Develop, edit, and maintain high-quality documentation ... including validation protocols (IQ/OQ/PQ), SOPs, work instructions, and technical reports + Collaborate with cross-functional teams including Quality, Engineering, Regulatory, and Manufacturing to gather source material and ensure accuracy + Translate complex… more
    Capgemini (08/30/25)
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