• Associate/Sr. Associate Manufacturing Scientist…

    Lilly (Lebanon, IN)
    …TS/MS (Technical Services/ Manufacturing Sciences), Quality Control , Quality Assurance, or Development. + Familiarity with cGMP manufacturing environment ... modeling and/or production data analysis) to improve and optimize process control , yield, purity, and/or productivity. In addition, the manufacturing scientist… more
    Lilly (10/15/25)
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  • Associate Director, QA Engineering - Combo…

    United Therapeutics (Research Triangle Park, NC)
    …Responsibilities for this role also include oversight and leadership of the Change Control , Quality Event, and CAPA programs and supporting management during ... and prioritize workloads, stressful situations, and deadlines + Demonstrated expertise with FDA Quality System regulations and cGMP , ISO 13485, ISO 14971, ISO… more
    United Therapeutics (09/26/25)
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  • Senior Project Manager - Life Sciences…

    CBRE (San Juan, PR)
    …delivery resource requirements, cost estimates & budget, work plan schedule & milestones, quality control , and risk identification. + Define the project delivery ... the programming, design, and construction phases on life science projects including laboratory research facilities. Experience with ** cGMP facilities** is a… more
    CBRE (09/30/25)
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  • Manager, QC Chemistry - Combo Products

    United Therapeutics (Research Triangle Park, NC)
    …tools, etc. + Technical and leadership experience in GMP, small molecule, pharmaceutical Quality Control laboratory + Experience developing and validating ... an environment where you can be both hands-on supporting Quality Control testing as well as build...of chemists and biochemists in the Combination Products QC laboratory , defining and proposing solutions for technical problems within… more
    United Therapeutics (09/24/25)
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  • Production Operator

    Lilly (Indianapolis, IN)
    … quality events in a timely manner. + Coordinate production activities with Quality Control , Quality Assurance, and Plant Maintenance to facilitate ... principles. + Segregate, label, and document rejected materials for quality review and disposition. + Support deviation reporting, CAPA...clear and concise manner. + Maintain accurate and complete lab data notebooks as per cGLP and/or cGMP… more
    Lilly (10/09/25)
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  • Quality Auditor, Second Shift

    Henkel (Geneva, NY)
    …and make an impact at Henkel. **What you'll do** + Perform regular quality control inspections, including but not limited to quantitative dimensional testing ... acceptance decision based on test results. + Perform regular quality control inspections throughout the production run...+ Must demonstrate good teamwork ability. + Knowledge of cGMP requirements is a plus + Strong attention to… more
    Henkel (09/18/25)
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  • Quality Assurance Manager (Nutraceuticals)

    Gummi World (Chandler, AZ)
    …as well as quality and regulatory agencies and manage a staff of both quality assurance and quality control technicians. The individual in this position ... compliance with industry standards for food and dietary supplements ( cGMP , GLP, CFR 100, CFR 111, HACCP, FSMA, SQF,...customer & other regulatory agency audits & escalates any quality control and food safety issues and… more
    Gummi World (10/04/25)
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  • Sr. Operator, Production Technician

    Lilly (Indianapolis, IN)
    … quality events in a timely manner. + Coordinate production activities with Quality Control , Quality Assurance, and Plant Maintenance to facilitate ... met. + Collaborate with maintenance technicians, equipment manufacturers, and quality assurance to ensure that all production equipment is...clear and concise manner. + Maintain accurate and complete lab data notebooks as per cGLP and/or cGMP… more
    Lilly (10/09/25)
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  • Production Operator

    Lilly (Indianapolis, IN)
    … quality events in a timely manner. + Coordinate production activities with Quality Control , Quality Assurance, and Plant Maintenance to facilitate ... met. + Collaborate with maintenance technicians, equipment manufacturers, and quality assurance to ensure that all production equipment is...clear and concise manner. + Maintain accurate and complete lab data notebooks as per cGLP and/or cGMP… more
    Lilly (10/08/25)
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  • Scientist III, Particles Manufacturing

    ThermoFisher Scientific (Fremont, CA)
    …documentation adhered to standard operating procedures (SOP) and current good manufacturing practices ( cGMP ) with the highest level of quality and compliance in ... Manufacturing Practices (GMP) Safety Standards, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Some degree of PPE (Personal Protective Equipment)… more
    ThermoFisher Scientific (10/02/25)
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