• Clinical Content Specialist

    Teleflex (Morrisville, NC)
    …or technical content is strongly preferred * Responsible for performing all duties in compliance with FDA 's Quality System Regulation (QSR), ISO13485, the ... medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in… more
    Teleflex (09/03/25)
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  • Medical Director, Interventional Urology…

    Teleflex (Wayne, PA)
    …needs with available internal resources. * Responsible for performing all duties in compliance with FDA 's Quality System Regulation (QSR), ISO13485, the ... medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in… more
    Teleflex (07/08/25)
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  • Quality Assurance Manager

    Katmai (Brilliant, OH)
    **SUMMARY** Responsible for the implementation, monitoring and maintenance of the Quality System in accordance with FDA Medical Device and Drug regulations. ... procedures, such as the Quality Manual and Quality System Procedures. + Ensure compliance with...and Documentation Control. + Prepare documentation and systems for compliance with the FDA requirements. + Conduct… more
    Katmai (08/08/25)
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  • Future Opportunities - Join Our Talent Pipeline…

    AbbVie (Irvine, CA)
    …communication skills. Additional Requirements: * Responsible for performing all duties in compliance with FDA 's Quality System Regulation (QSR), ISO13485, ... the Canadian Medical Device Regulations, and all other international regulatory requirements with which ZELTIQ complies. Additional Information All your information will be kept confidential according to EEO guidelines. Salary: $35,000 - $172,500 AbbVie is an… more
    AbbVie (06/19/25)
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  • Future Opportunities - Join Our Talent Pipeline…

    AbbVie (Pleasanton, CA)
    …communication skills. Additional Requirements: * Responsible for performing all duties in compliance with FDA 's Quality System Regulation (QSR), ISO13485, ... the Canadian Medical Device Regulations, and all other international regulatory requirements with which ZELTIQ complies. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or… more
    AbbVie (06/19/25)
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  • Senior Director, Global Quality

    Celestica (Maple Grove, MN)
    …* Experience with FDA and regulatory inspections. * In-depth knowledge of quality management systems and global compliance . * Experience in the HealthTech ... large global organization, collaborating with customers, suppliers, and partners, and ensuring compliance with regulatory requirements ( FDA , ISO, ASQ, RAC). The… more
    Celestica (08/28/25)
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  • Quality Assurance Engineer

    ZOLL Medical Corporation (Pawtucket, RI)
    …activities, including resolution of product nonconformities * Adhere to and ensure compliance with Quality System SOPs, work instructions, drawings, Good ... Manufacturing Practices (GMP), ISO, and FDA requirements * Participate in Risk Management activities *...resolution of product nonconformities * Adhere to and ensure compliance with Quality System SOPs, work instructions,… more
    ZOLL Medical Corporation (09/06/25)
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  • Senior Compliance Software Engineer…

    Abbott (Alameda, CA)
    …+ Coordinates the development and maintenance of departmental operating procedures to ensure compliance to relevant FDA , QSR, ISO guidelines, including 21 CFR ... Our 114,000 colleagues serve people in more than 160 countries. **Senior Compliance Software Engineer (Product)** **Working at Abbott** At Abbott, you can do… more
    Abbott (09/05/25)
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  • Sr. Quality Systems Documentation…

    Terumo Medical Corporation (Elkton, MD)
    …ID: 5082 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: Quality Systems & Compliance Terumo Medical Corporation (TMC) develops, ... quality processes and systems, enhancing team competencies and ensuring compliance with established standards and procedures. + Quality System Documentation… more
    Terumo Medical Corporation (08/19/25)
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  • Sr. Quality Engineer

    Medtronic (Minneapolis, MN)
    …in Fridley, MN. Responsible for New Product Development (NPD) Systems Engineering, quality assurance, and regulatory compliance within the medical device ... close on - 14 Oct 2025 **Position Description:** Sr. Quality Engineer for Covidien, LP (a Medtronic company) located...and risk documents including (PHA, DFMEA and PFMEA) in compliance with the requirements of ISO 14971, ISO 13485,… more
    Medtronic (08/12/25)
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