• Jt772 - Sr. Software Quality Engineer

    Quality Consulting Group (Juncos, PR)
    QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and ... including requirements, design, development, documentation, integration, test, verification and validation . + Defines appropriate measures to ensure product quality.… more
    Quality Consulting Group (08/28/25)
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  • Engineer - TS/MS Device Assembly & Packaging, DPEM

    Lilly (Indianapolis, IN)
    …failure modes of the process + Knowing the product process, development and validation history + Translating process requirement and education to the Joint Process ... and sterility and Bioburden control (for parenteral product) strategies and validation process (PV/PPQ) and oversight any documentation associated as required. +… more
    Lilly (08/26/25)
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  • Senior Quality Engineer I - Design & Reliability…

    Integra LifeSciences (Braintree, MA)
    …documentation such as product requirements, schematics, verification, and validation strategy/execution. + Coordinate, review and approve development documentation ... SPC programs with Manufacturing and Quality Control as a part of Process Validation and Design Transfer. + Maintains knowledge of and applies statistical analysis to… more
    Integra LifeSciences (08/08/25)
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  • Process Engineering Manager

    West Pharmaceutical Services (Williamsport, PA)
    …role requires deep technical expertise in injection molding and process validation within a regulated, high-precision environment. The ideal candidate will ensure ... manage a team of process engineers, process engineering technicians, and validation technicians. + Develop, validate, and optimize molding processes using scientific… more
    West Pharmaceutical Services (07/18/25)
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  • Controls Software Engineer

    Actalent (Columbus, OH)
    …are seeking an experienced Controls Software Engineer to join a leading pharmaceutical manufacturing company in Columbus, Ohio. This organization is renowned for ... producing over 750 high-quality generic, specialty, and branded pharmaceutical products relied upon by hospitals, physicians, and pharmacists across North America,… more
    Actalent (09/14/25)
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  • Chemist

    Actalent (Mount Prospect, IL)
    …FT-IR, UV-Vis, and pH meters. + Inspect supplies and ingredients for pharmaceutical product production. + Review Standard Operating Procedures (SOPs) and laboratory ... protocols for accuracy. + Perform some instrument validation . + Ensure adherence to GMP and FDA guidelines....+ 3-5+ years of experience with HPLC/GC in a pharmaceutical and cGMP setting. + Bachelor's degree with a… more
    Actalent (09/11/25)
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  • Associate Director, Product Quality

    AbbVie (Waltham, MA)
    …agency regulations worldwide. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), Intermediates, and Drug Products produced by ... Operations Management, Regulatory, Operations, or Technical Support in a pharmaceutical setting. Required regulatory inspection experience with direct interaction… more
    AbbVie (07/11/25)
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  • Associate Scientist

    Actalent (Birmingham, AL)
    …and skilled Associate Scientist with experience in microbiological testing and validation support. This role involves performing routine testing activities and ... + Perform sample shipments to contract testing laboratories. + Support validation by conducting bioburden swab testing, biological indicator testing, and endotoxin… more
    Actalent (09/14/25)
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  • Portfolio Controls Office Delivery Team Lead

    Turner & Townsend (Indianapolis, IN)
    …controls plans (cost, schedule, change, risk, earned value, invoice validation , communications, document management). + Collaborate with Capital Procurement on ... in estimating, budgeting, forecasting, earned value, contracts, invoice and change validation , risk management, and reporting for mega projects ($3B+) + Comfortable… more
    Turner & Townsend (09/12/25)
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  • Associate Director, Quality

    Curia (Albany, NY)
    …operational excellence; * Establish and maintain an efficient and compliant validation program including computer software validation and instrument ... well as the review of SOPs, investigations, specifications, methods, validation reports, and analytical reports; * Along with the...8 years of experience as a chemist in the pharmaceutical or biotechnology industry, which includes 2 years of… more
    Curia (09/11/25)
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