• Field Services Rep II

    Medtronic (MN)
    …to read and understand schematics and engineering drawings. + Familiar with the FDA 21 CFR, CGMP for Medical devices. + Excellent analytical and communication skills ... interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements… more
    Medtronic (01/09/26)
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  • Clinical Risk Management Analyst (RN) - Day Shift,…

    Trinity Health (Syracuse, NY)
    …visitors, vendors, various regulatory and professional agencies. **SUPERVISED BY:** Manager of Risk Management **SUPERVISES:** None **CAREER PATH:** Management ... as needed, including, but not limited to: the NYS Department of Health (DOH), FDA , and others. + Coordinates overall functions including but not limited to: NYPORTS,… more
    Trinity Health (01/09/26)
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  • Senior Principal Electrical Engineer

    Medtronic (Northridge, CA)
    …reviews and risk analysis activities **Regulatory & Quality:** + Ensure designs comply with FDA regulations (21 CFR Part 820), IEC 60601, and ISO 13485 + Support ... interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements… more
    Medtronic (01/09/26)
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  • Quality Manufacturing Representative (Day Shift)

    BD (Becton, Dickinson and Company) (Canaan, CT)
    …with resolving quality-related challenges. This role reports directly to the Quality Manager . **Job Description** We are **the makers of possible** BD is one ... understanding of quality control principles and manufacturing processes. + Knowledge of FDA regulations, GMP, ISO, OSHA and other applicable regulations required +… more
    BD (Becton, Dickinson and Company) (01/09/26)
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  • Analytical Chemist

    Corteva Agriscience (Indianapolis, IN)
    …Quantitative analytical experience in a governmental regulated environment, such as EPA, FDA , EU regulatory bodies or equivalent. + Regulatory analytical molecule ... manager , subject matter expert, focal point or related experience. \#LI-BB1 **Benefits - How We'll Support You:** + Numerous development opportunities offered to… more
    Corteva Agriscience (01/09/26)
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  • 3rd Shift Sanitation Supervisor

    Conagra Brands (Darien, WI)
    Reporting to the Sr Food Safety Quality and Regulatory Affairs Manager , you will take the lead on 3rd shift in ensuring our Birds Eye Food facility in Darien, WI is ... Manufacturing Practices (GMPs) + Hands-on experience with HACCP Plans and regulatory compliance ( FDA , USDA) + Technical expertise in Clean In Place (CIP) and Clean… more
    Conagra Brands (01/09/26)
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  • Business Development Representative, Informatics…

    Abbott (Mobile, AL)
    …decentralized locations in collaboration with the Centralized Informatics Account Manager . + Proactively identifies opportunities or acts upon previously identified ... and effectiveness of ARDx Informatics' Quality Management System per ISO, FDA and other regulatory agencies. + Identifies and facilitates cross-sell and… more
    Abbott (01/09/26)
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  • Quality Team Lead (Supervisor) - 3rd Shift

    Conagra Brands (Denver, CO)
    Reporting to the Quality Manager , you will lead the Quality Assurance team at our Denver Plant, producers of Udi's Gluten Free products. You will supervise and guide ... safe practices * Strong understanding of HACCP plans and government regulations ( FDA , USDA) * Excellent interpersonal and communication skills * Proficiency in… more
    Conagra Brands (01/09/26)
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  • Thought Leader Liaison, PAH / PH-ILD

    Chiesi (Cary, NC)
    …created position will initially focus on pre-launch preparation in anticipation of FDA approval of our PAH/PH-ILD collaboration asset. They work closely with ... and attend advisory boards as appropriate. + Coordinate with Market Development Manager and Speaker Programs Management on KOL Speaker bureau relationships including… more
    Chiesi (01/09/26)
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  • Director IT Engineering

    Regeneron Pharmaceuticals (Warren, NJ)
    …6 years' experience as Software Developer and 3 years' experience in an FDA or similarly regulated environment or equivalent combination of education and experience. ... required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron's on-site policy and expectations for your… more
    Regeneron Pharmaceuticals (01/09/26)
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