• Jt800 - Supplier Quality Engineer I

    Quality Consulting Group (Villalba, PR)
    QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... + Technical writing knowledge + Organization and Communication skills + Process Validation and Computer software knowledge + Shift: 1st Quality Consulting Group, LLC… more
    Quality Consulting Group (09/13/25)
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  • Senior Scientist, External Manufacturing MS&T…

    J&J Family of Companies (Raritan, NJ)
    …Degree in Science/Engineering or Equivalent with 4-6 years of Biotech/ Pharmaceutical experience or equivalent industry experience. + Prior work experience in ... advanced therapies (ie cell/gene therapy products, vaccines) product regulatory and validation requirements + Experience in a Cell/Gene Therapy cGMP manufacturing… more
    J&J Family of Companies (09/13/25)
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  • Summer 2026 Intern - Digital-Automation QV

    Sanofi Group (Swiftwater, PA)
    …Report, Test Script, and Datapack + Coordinate update of a maintained validation plan/strategy + Demonstrate knowledge of quality organization and QV's role in ... not require company sponsorship** **Preferred Qualifications:** + Experience in pharmaceutical /biopharmaceutical industry or related industry/manufacturing environment + Exceptional organizational,… more
    Sanofi Group (09/12/25)
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  • Process Engineer 2026 Summer Intern

    J&J Family of Companies (Jacksonville, FL)
    …the most significant healthcare challenges. Our Corporate, Medical Devices, and Pharmaceutical teams leverage data, real-world insights, and creative minds to make ... identify process bottlenecks and potential areas for optimization + Support process validation and documentation activities + Participate in root cause analysis and… more
    J&J Family of Companies (09/12/25)
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  • Senior Automation Engineer

    Pfizer (Rocky Mount, NC)
    …small project teams. + Monitor, generate and complete the periodic review, validation master plan for the automation engineering program. + Demonstrate good ... effectiveness and communication skills {written and oral} **Nice-to-Have** + Relevant pharmaceutical experience + The ideal candidate should have background in cGMP… more
    Pfizer (09/12/25)
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  • Quality Engineer II

    Abbott (Alameda, CA)
    …and other release documentation for products used in design verification/ validation testing, clinical investigations, research use and demonstration purposes. + ... 2 years' experience in regulated environment such as medical devices or pharmaceutical products. + Knowledge of medical device standards including FDA QSR, ISO… more
    Abbott (09/12/25)
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  • Coordinator I - Clinical Research

    HonorHealth (AZ)
    …in many of the data related activities: CRF tracking, reviewing validation , updating, SAE reconciliation, lab data reconciliation, resolve queries and safety ... research or data management experience - Required Other Experience in pharmaceutical sponsored and investigator initiated clinical research trials in the therapeutic… more
    HonorHealth (09/12/25)
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  • Analyst, Government Pricing

    IQVIA (Milwaukee, WI)
    …to validate calculation accuracy and system performance. + Perform data validation , transformation, and reconciliation across multiple data sources including general ... as required by client engagements. Preferred Qualifications: + Experience with pharmaceutical pricing systems or regulatory compliance platforms. + Familiarity with… more
    IQVIA (09/12/25)
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  • Associate Director - SAP & Supply Chain Systems

    Lilly (Lebanon, IN)
    …to drive business process optimization. + Adhere to corporate computer systems validation policies and procedures. + Be an advocate for supply chain efficiencies ... + Minimum of 5 years' experience in manufacturing, preferred in pharmaceutical or other regulated industries. + Experience with integrated business process… more
    Lilly (09/12/25)
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  • Design Quality Engineer

    J&J Family of Companies (Danvers, MA)
    …product requirements. + Participate in V&V activities, review verification and validation plan, test protocol reports. + Participate in product cybersecurity ... master's degree in engineering or scientific discipline. Medical Device and/or pharmaceutical industry is preferred. + Knowledge of quality system regulation,… more
    J&J Family of Companies (09/12/25)
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