• Lead Phlebotomist

    Grifols Shared Services North America, Inc (Athens, GA)
    …familiarity and compliance with all state and federal regulations, FDA -approved Standard Operating Procedure Manual, Occupational Safety and Health Administration ... Reports all unsafe situations or conditions to area lead, supervisor or manager . Primary Requirements: Additional Responsibilities Cross trained and works in other… more
    Grifols Shared Services North America, Inc (12/17/25)
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  • Branch Coordinator - TELEWORK

    Owens & Minor (Tampa, FL)
    …support to the daily operations of the Branch Office and Branch Manager (s). This role is eligible for telecommuting. **ESSENTIAL DUTIES AND RESPONSIBILITIES** + ... + **PREFERRED QUALIFICATIONS** **SKILLS, KNOWLEDGE AND ABILITIES** + Knowledge of DOT/ FDA Regulations. + **Language Skills** + Bilingual (reading, writing, verbal).… more
    Owens & Minor (12/17/25)
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  • Project Engineer

    Caldera Medical (Westlake Village, CA)
    …- To Improve the Quality of Life for Women! Message from the Hiring Manager : The Project Engineer will lead projects and provide technical expertise to ensure the ... design, and manufacturing. A comprehensive understanding of ISO, GMP and FDA regulations for the development. Other Requirements: 1. Strong analytical and… more
    Caldera Medical (12/17/25)
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  • Senior Chemist

    ADM (Kennesaw, GA)
    …under cGMP/GLP environment as per company's standard operating procedures and USP/ FDA guidelines. + Assist Lab Administrator with scheduling analytical tests and/or ... equipment + Schedule and assist equipment repair technicians. + Assist Lab Manager with development of Capex requests. **Training and Proficiency** + Develop and… more
    ADM (12/17/25)
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  • Specialist QA |

    Mentor Technical Group (Gurabo, PR)
    …provides a comprehensive portfolio of technical support and solutions for the FDA -regulated industry. As a world leader in life science engineering and technical ... Lead site audits. + Own site quality program procedures. + Designee for QA manager on local CCRB. + Review Risk Assessments. + Support Automation activities. +… more
    Mentor Technical Group (12/17/25)
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  • Account Executive, Surgery Ultrasound…

    Fujifilm (Columbus, OH)
    …to cross sell additional products and options. + Work Hospital Relations Manager , National and Government Accounts to develop relationships and implement hospital ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
    Fujifilm (12/16/25)
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  • Warehouse Associate (Medical Imaging Company,…

    Fujifilm (Macedonia, OH)
    …material neatly in designated area. + Order warehouse supplies through request to Manager of Warehouse. + Assist with the Physical Counts of Inventory: + Check ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
    Fujifilm (12/16/25)
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  • Operator I

    Teva Pharmaceuticals (Edison, NJ)
    …Operators as required. * Perform additional duties as assigned by Supervisor or Manager . * Must be able to read, write, speak, and comprehend English. **Your ... or Equivalent Required Experience Required: * 1-2 years' experience in FDA regulated packaging environment desired. Specialized or Technical Knowledge, Licenses,… more
    Teva Pharmaceuticals (12/16/25)
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  • Supervisor, Packaging Operations - Pharma

    Gilead Sciences, Inc. (La Verne, CA)
    …and conducts final reviews prior to batch release approval by manager Supervises personnel including organizing and prioritizing daily tasks, performing training ... Proficiency in Microsoft Office applications. Must possess a strong knowledge of the FDA and cGMP standards as well as regulatory guidance documents. 6+ years of… more
    Gilead Sciences, Inc. (12/16/25)
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  • Senior Specialist, Quality Assurance

    Cardinal Health (Louisville, KY)
    …(QAS) performs all quality review and approval/release decisions at an FDA -regulated drug manufacturing facility. The facility manufactures two sterile liquid ... metrics related products and processes as deemed necessary by the Regional Quality Manager RQM. + Ensures the site manufactures products to meet the requirements of… more
    Cardinal Health (12/16/25)
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