• Senior Director, Data Quality and Integrity,…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical ... to deliver innovative data solutions, integrates AI technologies, and drives process improvements. Collaborating with the Global QMS eCompliance team, the director… more
    Daiichi Sankyo Inc. (06/04/25)
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  • Automation Engineer, Delta V

    J&J Family of Companies (Wilson, NC)
    …Automation professionals with various technical expertise, responsible for the implementation, validation , qualification and maintenance of the ISA-95 level 1 and 2 ... V network infrastructure. The new facility and the production process are envisioned to be highly automated with data...lead execution system code change. + Write and perform validation protocols. + Ensure compliance with global standards. +… more
    J&J Family of Companies (06/04/25)
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  • Commissioning Project Manager

    VTI Life Sciences (Los Angeles, CA)
    …excellence by providing Commissioning, Qualification, Quality Engineering, Automation and Validation Services to the Pharmaceutical , Biotechnology, Biologics and ... and ambitious engineers looking to accelerate their career in the pharmaceutical , biotechnology and medical device industries. We offer an opportunity to… more
    VTI Life Sciences (06/03/25)
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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 ... consumer and Catalent employee. **The Role** + Enforce Computerized System Validation (CSV) guidelines, policies, and procedures for control systems, automation,… more
    Catalent Pharma Solutions (05/22/25)
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  • Associate Design Quality Engineer

    Abbott (Temecula, CA)
    …actively participate in product development and transfer activities, ensuring product and process conformance to FDA and ISO 13485 standards. Review validation ... and risk management. . Acts as a reviewer and approver of validation methods and protocols, test methods, statistical analysis methods and specification development.… more
    Abbott (05/06/25)
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  • Automation Engineer III

    Sanofi Group (Framingham, MA)
    …infrastructure + Experience with systems/network/ validation , preferable in the chemical, pharmaceutical , foods, or other process industries is preferred + ... a new or revised digital systems, the design, installation, verification and validation of the system, the maintenance of the system in its… more
    Sanofi Group (05/25/25)
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  • Quality Manager

    Insight Global (Easthampton, MA)
    …Strong knowledge of pharmaceutical manufacturing processes, computer and equipment validation , GMPs, and product/ process validation - People-management ... Manager for our client, a key partner in the pharmaceutical sector, based in Easthampton, MA. This Quality Manager...due to a disability during the application or recruiting process , please send a request to Human Resources Request… more
    Insight Global (06/11/25)
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  • Senior Specialist, Conformance

    Bayer (Berkeley, CA)
    … and/or biotechnology experience including GM manufacturing, deviation investigation, process monitoring, project management and validation experience or ... + Ability to expand capabilities across operations support team (ie, Conformance, Process Monitoring and GMP Projects) and other areas of biologics manufacturing… more
    Bayer (06/05/25)
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  • Manager, QC LIMS

    Fujifilm (Holly Springs, NC)
    …efficiency o Identify and assess opportunities for improving the LIMS implementation process o Develop, implement,, and review validation protocols, SOPs, test ... to foster professional development * Participates in the recruitment process and retention strategies to attract and retain talent,...experience in a GMP environment and LIMS experience in pharmaceutical industry OR * Master's degree with 5+ years… more
    Fujifilm (06/03/25)
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  • Director, Manufacturing Engineering

    ThermoFisher Scientific (Cincinnati, OH)
    …of the site co-op program. + Directs and leads the technical aspects ( process , equipment, automation, cleaning, validation programs, process maintenance, and ... pharmaceuticals are made with a simplified, end-to-end supply chain for pharmaceutical and biopharmaceutical companies of all sizes. **Position summary** The… more
    ThermoFisher Scientific (05/30/25)
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