• Supervisor, Utility Maintenance

    Fujifilm (Holly Springs, NC)
    …electrical, plumbing, chemical treatment, and control systems + Familiarity with GMP , FDA , and other regulatory requirements + Effective communication, ... ensuring compliance with safety, regulatory, and Good Manufacturing Practices ( GMP ) standards. Additionally, this role also provides training, technical support,… more
    Fujifilm (07/31/25)
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  • Packaging Tech 1-Night Shift

    BioFire Diagnostics, LLC. (Durham, NC)
    …following OSHA regulations (LOTO, electrical safety, etc.) preferred. + Knowledge of FDA and/or GMP regulations preferred. + Mechanical background preferred. + ... Ability to rapidly learn new procedures and reduce them to practice. + Must be able to learn, comprehend and demonstrate competency in operating new equipment within a 75-day period of working with a trainer. #biojobs more
    BioFire Diagnostics, LLC. (08/23/25)
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  • Packaging Operations

    ManpowerGroup (Mebane, NC)
    …and inspecting products. + Maintain accurate records and logs in accordance with FDA and GMP regulations. + Follow standard operating procedures (SOPs) and ... adhere to safety and quality guidelines. + Communicate effectively with team members and supervisors. + Work collaboratively in a team setting to meet production goals. **What's Needed?** + High school diploma or equivalent required. + Entry-level; some… more
    ManpowerGroup (08/22/25)
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  • Manufacturing Cleaning Tech 1 - 2nd Shift

    BioFire Diagnostics, LLC. (Durham, NC)
    …following OSHA regulations (LOTO, electrical safety, etc.) preferred. + Knowledge of FDA and/or GMP regulations preferred. + Mechanical background preferred. + ... Ability to rapidly learn new procedures and reduce them to practice. + Must be able to learn, comprehend and demonstrate competency in operating new equipment within a 75-day period of working with a trainer. + Reasonable, reliable attendance and punctuality… more
    BioFire Diagnostics, LLC. (07/31/25)
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  • Assistant/ Associate Biochemist

    Grifols Shared Services North America, Inc (Clayton, NC)
    …learning and mastering manual and automated testing procedures conducted within an FDA regulated GMP /GLP environment. Performs biological testing of moderate to ... advanced complexity within the **QC Biochemistry Laboratory Animal Facility.** Manual Laboratory testing methods revolve around animal testing using rabbits, guinea pigs, and mice. Animal handling experience is required. Responsibilities also include sample… more
    Grifols Shared Services North America, Inc (07/23/25)
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  • Assistant/Associate Biochemist

    Grifols Shared Services North America, Inc (Clayton, NC)
    …learning and mastering manual and automated testing procedures conducted within an FDA regulated GMP /GLP environment. Performs biological testing of moderate to ... advanced complexity within the QC Biochemistry Laboratory. Manual Laboratory testing methods revolve around 96 well, plate-based testing, using single and multi-channel pipettes for serial dilutions. Other testing procedures involve automated analyzers for… more
    Grifols Shared Services North America, Inc (07/23/25)
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  • Quality Documentation Specialist

    Kelly Services (Wilson, NC)
    …experience within the pharmaceutical or biologics industry. + Strong knowledge of FDA /EMEA regulations and GMP standards. + Hands-on experience with electronic ... by managing and maintaining controlled documents such as SOPs and GMP -regulated materials. + Administer and troubleshoot the site's Electronic Document Management… more
    Kelly Services (08/08/25)
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  • Process Engineer Lead, Liquids

    Reckitt (Wilson, NC)
    …with liquid and oral solid dosage (OSD) forms. + Strong understanding of GMP , FDA regulations, and pharmaceutical manufacturing standards. + Hands-on experience ... + Compliance & Documentation: Ensure all processes comply with cGMP, FDA , and Reckitt quality standards. Maintain accurate and complete documentation (batch… more
    Reckitt (07/14/25)
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  • CAD Designer

    System One (Sanford, NC)
    …manage multiple projects and priorities in a fast-paced environment. + Familiarity with GMP , FDA , or other regulatory standards is a plus. Preferred Experience: ... + 3+ years of experience in CAD drafting, project coordination, and/or project management. + Experience in pharmaceutical, biotech, or industrial engineering environments. + Understanding of capital project workflows, documentation control, and project… more
    System One (08/21/25)
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  • CAD Design Engineer

    Insight Global (Sanford, NC)
    …environments. Familiarity with capital project workflows and documentation control. Knowledge of GMP , FDA , or other regulatory environments is a plus null ... We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified… more
    Insight Global (08/16/25)
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