• Analyst I Postmarket Surveillance

    Abbott (Plano, TX)
    …patients throughout the pain continuum. Under the direction of the department manager , the Postmarket Surveillance Analyst I may perform two different functions ... report needs to be filed with various global regulatory agencies (eg, FDA , European Competent Authorities) and sends reports within required timeframes. Prepares… more
    Abbott (01/09/26)
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  • Biomedical Field Service Engineer - Chicago

    BD (Becton, Dickinson and Company) (Sparks, MD)
    …www.bd.com. Job Title: Field Service Engineer Location: Reports To: District Field Service Manager Overview: Join our dynamic Field Service Team as a Field Service ... * Documentation: Complete service administration activities promptly, adhering to ISO, FDA , and BD policies. Qualifications: * Associate's degree or Technical School… more
    BD (Becton, Dickinson and Company) (01/09/26)
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  • Analytical Chemistry Laboratory Supervisor

    Teleflex (Morrisville, NC)
    …Test Method Validation (TMV) and analytical method transfer activities consistent with FDA , ICH (Q2/Q14), and ISO 17025 principles. The role will oversee test ... and reliable delivery of analytical services to internal stakeholders. As a People Manager , you play a pivotal role in leading, developing, and inspiring a… more
    Teleflex (01/09/26)
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  • Associate Staff Engineer - Sustaining

    BD (Becton, Dickinson and Company) (Salt Lake City, UT)
    …should have experience in medical device industry or related field. Knowledge of FDA regulations, IEC standards, ISO 10993, and quality system requirements such as ... user documentation (eg, specifications, protocols, reports) according to applicable FDA regulations, IEC standards, ISO 10993, and quality system requirements.… more
    BD (Becton, Dickinson and Company) (01/07/26)
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  • Manufacturing Supervisor

    PCI Pharma Services (Bedford, NH)
    …a manufacturing team in a variety of complex tasks in accordance with the FDA and other regulatory agencies while following all safety guidelines of PCI. They will ... capacity demands + Guide and train employees to ensure FDA and other regulatory agency requirements have been properly...communicating the status of all projects to their Manufacturing Manager + Interacts with cross functional support teams such… more
    PCI Pharma Services (01/07/26)
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  • Design Control Engineer/Specialist

    GE HealthCare (Cleveland, OH)
    …an effective design, development, and transfer process that adheres to applicable FDA , EU regulations, ISO 13485:2016, and other governing regulations applicable to ... building compliant new product development processes with adherence to FDA Design Control requirements and Risk Management ISO standards....other areas of the QMS as directed by the manager . **What You'll Need:** + Bachelor's degree from an… more
    GE HealthCare (01/03/26)
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  • Quality Engineer II | M-F | Pay Based…

    Katecho (Des Moines, IA)
    …operations, personnel management, and adherence to and administration of ISO 13485 and FDA , Title 21 Part 820, QSR. 4. Works with other departments to determine ... 9. Audits Business Management Systems, ie ISO 13485 and FDA , Title 21 Part 820, QSR, etc. at Katecho...effectively present information and respond to questions from customers, manager , and employees. * Must complete a Non-Compete Agreement… more
    Katecho (01/03/26)
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  • System Director Of Quality Assurance - Memorial…

    Compass Group, North America (Houston, TX)
    …17,000 professional food service team members. **Job Summary** **The Quality Assurance Manager ** is responsible for development and maintenance of all QA programs, ... meeting USDA, FDA and customer requirements and ensuring the quality and...prerequisite food safety standards are met according to USDA, FDA , FSIS, FSMA and corporate requirements. + Must have… more
    Compass Group, North America (12/31/25)
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  • Sr./System Account Executive- Sutter Gould,…

    Boehringer Ingelheim (Modesto, CA)
    …specialist role responsible for pull-through of the account plan (developed by the Account Manager ) at the Health System's various sites of care and with the Health ... Company business in accordance with all regulations (eg, EEO, FDA , DEA, OSHA, PDMA, EPA, PhRMA, etc.) and Company...Previous account management experience. * Various regulations (eg, EEO, FDA , DEA, OSHA, PDMA, EPA, PhRMA, etc.) and Company… more
    Boehringer Ingelheim (12/24/25)
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  • Nuclear Manufacturing Supervisor

    Cardinal Health (East Hartford, CT)
    …sensitive radiopharmaceuticals in an integrity driven, highly regulated environment (ie FDA , NRC, DOT) to support patient treatment through disease diagnosis, ... compliance with all regulatory standards including EHS, cGMP, Radiation Safety, applicable FDA and pharmacy laws, DOT, and internal policies and interpretations +… more
    Cardinal Health (12/23/25)
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