• Jt009 - Manufacturing Engineer II

    Quality Consulting Group (Villalba, PR)
    …manufacturing industry in Puerto Rico & USA. Responsibilities: + Must have knowledge in Process Validation , Equipment IQ and Computer software validation . + ... QUALITY CONSULTING GROUP, a leader in the pharmaceutical , biotech, medical devices, and manufacturing industry, is...of 2 years of relevant experience. + Knowledge in Process Validation , Equipment IQ and Computer software… more
    Quality Consulting Group (12/02/25)
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  • Engineer, Quality, 3rd shift (Monday-Friday, 11…

    AbbVie (North Chicago, IL)
    …appropriate product/ process limits assigned. + Auditing of commissioning and validation documentation. + Develops product quality plans, documents and systems by ... Supports the Quality Engineering group by auditing of commissioning and validation documentation completed by others, authoring and execution of newly identified… more
    AbbVie (11/22/25)
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  • Associate Principal Scientist, Engineering

    Merck (Rahway, NJ)
    …Chemical Technology, Data Analysis, Detail-Oriented, Maintenance Supervision, Manufacturing Process Validation , Manufacturing Quality Control, Manufacturing ... experience to develop safe and robust manufacturing processes through process characterization, technology transfer, validation , filing and supply… more
    Merck (01/06/26)
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  • Associate Director - Drug Product External…

    Lilly (Indianapolis, IN)
    …responsibility for ensuring all products are manufactured according to a validated process , following the approved control strategy and maintaining in a validated ... to ensure reliable supply of medicines through effective and efficient manufacturing process . + Ensure capable and in control processes at CMs. Establish and… more
    Lilly (11/22/25)
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  • Marketing Manager, DSA - (Bioanalysis marketing…

    Charles River Laboratories (Wilmington, MA)
    …and sensitive compound detection throughout the development spectrum of: + Pharmaceutical products + Industrial chemicals + Agrochemical products + Manage Laboratory ... + Molecular Biology + Immunology + Biomarkers + Method Development and Validation + Non-GLP Discovery Bioanalysis **Job Qualifications** The following are minimum… more
    Charles River Laboratories (01/14/26)
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  • API Manufacturing Associate I (D - Night Shift)

    Novo Nordisk (Clayton, NC)
    …for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our ... injectable and oral treatment supply chains. Our newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of… more
    Novo Nordisk (01/07/26)
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  • Lead QA Technician

    ThermoFisher Scientific (Greenville, NC)
    …phase of drug development. With global operations, we support active pharmaceutical ingredients (APIs), biologics, cell and gene therapy, viral vectors, formulation, ... products. Our dedicated colleagues provide services including formulation development, process optimization, scale-up, sterile fill-finish, packaging, and labeling, ensuring… more
    ThermoFisher Scientific (12/25/25)
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  • Facilities Engineer III

    Gilead Sciences, Inc. (Foster City, CA)
    …possess a strong understanding of mission-critical facilities, laboratory, and pharmaceutical manufacturing environments and the unique demands placed on utility ... maintenance of HVAC and utility systems, preferably within mission-critical facility, pharmaceutical , or biotechnology industry. OR + Master's degree in Mechanical,… more
    Gilead Sciences, Inc. (12/10/25)
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  • GMP Senior Engineer (Electrical and Mechanical…

    Grifols Shared Services North America, Inc (San Diego, CA)
    …capital investments (engineering design, start-up and qualification of GMP process equipment). Assures continuous improvement of automated Filling, Labeling, ... related industry experience and at least 1 year of experience in pharmaceutical /biotech operations, with thorough working knowledge production unit operations and … more
    Grifols Shared Services North America, Inc (01/14/26)
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  • Associate Scientist

    Catalent Pharma Solutions (Winchester, KY)
    …work/assist on method development, method transfer, method verification and method validation under appropriate guidance along with routine release and stability ... of client's documents as required including but not limited to specification/ validation reports/test methods/compliance reports etc. to perform gap analysis with… more
    Catalent Pharma Solutions (01/14/26)
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