• Cleaning Validation Engineers

    VTI Life Sciences (Raleigh, NC)
    …end of the year (Initial Contract ) Job Title: Senior Cleaning Validation Engineer Industry: Pharmaceutical Manufacturing Level of Experience: 8+ years ... Validation Engineers to work onsite at our client's pharmaceutical manufacturing facility in the Raleigh, NC area. One...Contract ) Job Description + Looking for a Cleaning Validation Engineer, specifically for drug product parts washers. +… more
    VTI Life Sciences (05/17/25)
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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 (06/11/25)
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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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  • Senior Microbiology Analyst

    Glenmark Pharmaceuticals Inc., USA (Monroe, NC)
    …well-positioned to successfully emerge as a leading integrated research-based pharmaceutical company. POSITION SUMMARY: The Senior Microbiology Analyst is ... the Microbiology department + Limit outsourcing of microbiology testing to contract laboratory. Operational Excellence: + Perform sterility testing on raw materials,… more
    Glenmark Pharmaceuticals Inc., USA (07/24/25)
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  • Associate Director, Commercial Quality Assurance

    Catalent Pharma Solutions (Greenville, NC)
    …Quality Assurance** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... all commercial manufacturing and laboratory operations onsite and at contract organizations (CMOs and CPOs). **The Role** + Act...at least 7 years of professional experience in QA/QC pharmaceutical manufacturing or; + Master's degree with at least… more
    Catalent Pharma Solutions (07/29/25)
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  • Quality Engineer

    US Tech Solutions (Durham, NC)
    **Duration: 12-month contract ** **Job Description:** + Provide product team support including, Material Review Board (MRB), customer complaint activities, ... statistical analysis, validation support, inspection plans, metrology, quality metrics and report...a regulated industry such as health care, medical device, pharmaceutical , etc). **Skills:** + Good understanding of Continuous Improvement… more
    US Tech Solutions (07/18/25)
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  • Project Manager

    Catalent Pharma Solutions (Greenville, NC)
    …is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients ... is responsible for leading and directing multiple client projects within the contract manufacturing division. The Project Manager will work closely with key project… more
    Catalent Pharma Solutions (07/12/25)
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  • Automation Manager

    Pfizer (Rocky Mount, NC)
    …rates. You will manage all project phases, develop documentation, manage contract resources (when applicable), and provide troubleshooting support for systems within ... such as MS Word, Excel, PowerPoint. + Broad experience in a pharmaceutical environment with a hands-on understanding of control and data acquisition systems,… more
    Pfizer (07/30/25)
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  • Process Engineer Lead, Liquids

    Reckitt (Wilson, NC)
    …and efficient manufacturing processes are transferred into Production from R&D, contract manufacturers, or other Reckitt Sites. + Process Optimization: Analyze and ... troubleshooting process issues and implementing corrective actions. + Scale-Up & Validation : Support scale-up of new products from R&D to full-scale production,… more
    Reckitt (07/14/25)
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  • Associate Medical Director/Medical Director…

    ThermoFisher Scientific (Wilmington, NC)
    …reported by study sites. + Performs data review as specified in the client contract and data validation manual including review of coding listings and/or full ... as follows: + Suitable clinical trial experience in a Contract Research Organization, pharmaceutical company or as a principal investigator (comparable to 1-2… more
    ThermoFisher Scientific (07/15/25)
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