• (CQV) Lead Engineer

    WuXi AppTec (Middletown, DE)
    …) Lead Engineer to lead the execution of commissioning qualification, and validation activities at our pharmaceutical manufacturing facility. The CQV Lead ... technical discipline. * Minimum of 8-10 years of CQV or validation experience in the pharmaceutical or biotechnology industry. * Preferably at least 3 years in… more
    WuXi AppTec (09/20/25)
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  • Quality Engineer III

    ThermoFisher Scientific (Detroit, MI)
    …of 5 years prior experience in Quality related field including Quality Engineering and validation ( in a pharmaceutical or Life Science position preferred). + ... root cause analysis (RCAs) and implementing corrective/preventative (CAPAs) actions and applying validation principles. **What will you do?** + Use (RCA) methods and… more
    ThermoFisher Scientific (09/21/25)
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  • 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 (09/10/25)
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  • CSV Automation Specialist

    VTI Life Sciences (San Diego, 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 (08/13/25)
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  • Maintenance Manager

    Nestle (Anderson, IN)
    …Project + Competent design knowledge. AutoCAD knowledge. + Project Management in the pharmaceutical or food industry. + Process qualification, validation in the ... pharmaceutical or food industry IQ, OQ, PQ. + Knowledge on FDA & GMP/GAMP regulation. + In-depth knowledge of food processing Equipment Maintenance and Technology. + Applicable Maintenance techniques + Appropriate Maintenance execution + Knowledge of food… more
    Nestle (08/16/25)
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  • Manager, Microbiology

    Curia (Albuquerque, NM)
    …+ Previous experience managing Microbiology staff + Previous experience with pharmaceutical cleanroom environments + Proficient in the validation /qualification ... organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At… more
    Curia (07/25/25)
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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 (09/02/25)
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  • Senior Director, Site Quality Head, Goa

    Teva Pharmaceuticals (Parsippany, NJ)
    …as CMC content of regulatory submissions, + Deep knowledge of chemical/ pharmaceutical production operations/ lifecycle, production equipment/ validation and ... CAPA Creation and implementation; trending and metrics, compliance with validation requirements; verification that equipment, facility and utility systems are… more
    Teva Pharmaceuticals (09/06/25)
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  • QA Product Manager

    Catalent Pharma Solutions (St. Petersburg, FL)
    …training and/or equivalent combination of education and experience in the QA pharmaceutical industries. + Prior experience working with validation , manufacturing ... process improvement projects and Product Development Projects; c) all product process validation and cleaning validation documents; d) all Preventive Maintenance… more
    Catalent Pharma Solutions (09/03/25)
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  • Sr. Engineer - Automation Infrastructure

    Lilly (Indianapolis, IN)
    …technologies. + Small/medium project management or change management experience. + Pharmaceutical experience is desirable. + Computer System Validation ... experience is desirable. **Other Information:** + 8-hour days, after-hour support. + Occasional travel may be required for training, conferences, capital projects, etc. Lilly is dedicated to helping individuals with disabilities to actively engage in the… more
    Lilly (09/10/25)
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