• Sr. Environmental Safety & Health Specialist

    Pfizer (Rocky Mount, NC)
    …to use safety methodologies to ensure safe work practices throughout your assigned manufacturing area of responsibility. You should have the ability to coach and ... for colleagues and contractors. This position reports directly to the Senior Manager , Environmental, Health, & Safety. **How You Will Achieve It** + Provides… more
    Pfizer (09/13/25)
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  • Quality Engineer

    Actalent (St. Paul, MN)
    …Engineer to join our team and help drive excellence across product development and manufacturing . In this dynamic role, you will lead key initiatives such as part ... modified programs as directed by the Quality & Regulatory Manager . + Carry out Quality Planning including Process Flow...required. + 4 years of experience in a regulated manufacturing environment. + Experience in APQP, PPAP, and SPC… more
    Actalent (09/10/25)
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  • Facility Services Coordinator

    Amcor (Valdosta, GA)
    …other general repair skills. + Possesses knowledge of mandated regulations such as FDA , ISO, SQF rules and regulations, Good Manufacturing Practices, HACCP, Food ... safety topics as identified and assigned by the Production Manager . + Lock out tag out + HACCP +...to and enforces safety, food safety, quality, and Good Manufacturing Practices regulations. + Actively participates in SQF audits… more
    Amcor (09/05/25)
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  • Facilities Maintenance Associate II

    University of Colorado (Aurora, CO)
    …scheduling as per Gates Biomanufacturing facilities' standard operating procedure to meet FDA good manufacturing practice (GMP) compliance. + Participate in new ... and build out. + Report and take guidance and direction from the Facilities Manager , assisting in large scale capital projects, annual shutdowns, and other events. +… more
    University of Colorado (08/20/25)
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  • Environmental Health & Safety Specialist

    Danaher Corporation (Indianapolis, IN)
    …and six sigma tools for problem-solving, daily management, and Kaizen events. + FDA regulated industry or medical device manufacturing experience Travel, Motor ... is responsible ensuring all associates at our Indianapolis, Indiana manufacturing facility can safely help us achieve our mission...research, and medicine. This position reports to the EHS&S Manager , dotted Plant Director, and is part of the… more
    Danaher Corporation (07/24/25)
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  • Training Coordinator

    Kedplasma (Houston, TX)
    …the Center Manager . Operates within the scope of EU Guidance on Good Manufacturing Practices and FDA cGMP 21CFR. **ESSENTIAL JOB SUNCTIONS** Every effort has ... **Core** + Works in coordination with the Regional Field Training Manager for training-related initiatives. + Demonstrates competence and compliance with KEDPLASMA… more
    Kedplasma (09/12/25)
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  • QA Investigator III

    Actalent (St. Louis, MO)
    …investigations, root cause analysis, and execution of CAPAs in an FDA -regulated environment. + 3+ years of experience in a regulated pharmaceutical/chemical ... manufacturing environment preferred. Work Environment The role is based...investigations. The team consists of four investigators and a manager , and the environment may fluctuate between busy and… more
    Actalent (09/14/25)
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  • Quality Lead Tech

    BioLife Plasma Services (Camp Hill, PA)
    …according to tasks trained and assigned, to ensure that source plasma manufacturing is performed consistently according to current Good Manufacturing Practices ... Lead Technician. Demonstrated understanding of quality assurance in an FDA -regulated environment. + Effective communication, organizational, and technical/problem-solving skills.… more
    BioLife Plasma Services (09/14/25)
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  • Quality Assurance Supervisor

    Primo Brands (Lee, FL)
    …and water processing technician, and will report directly to the QA Manager . Responsibilities **Key responsibilities include but are not limited to the following:** ... Corporate and outside laboratories, and to external regulatory agencies ( FDA , IBWA, EPA, etc.). + May serve as plant...microbiology or related field preferred. + Prior QA or Manufacturing experience (3-5 years) required in lieu of degree.… more
    Primo Brands (09/13/25)
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  • QA Investigator III

    Actalent (St. Louis, MO)
    …in conducting investigations, root cause analysis, and execution of CAPAs in an FDA -regulated environment. + 3+ years of experience in a regulated pharmaceutical or ... chemical manufacturing environment preferred. + Ability to review, compile, and...team is small, consisting of four investigators and a manager , with the possibility of converting to a full-time… more
    Actalent (09/12/25)
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