• Director, Quality Engineering - WW IPD

    BD (Becton, Dickinson and Company) (Brea, CA)
    …field (advanced degree preferred). * Minimum 15 years of progressive experience in Design Quality Assurance within the medical device industry. * At least ... **Job Description Summary** The Director, Quality Engineering - WW IPD is responsible for...and technical QA staff. * Deep knowledge of global medical device regulations ( FDA , EU… more
    BD (Becton, Dickinson and Company) (08/28/25)
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  • Senior Quality Systems Specialist

    Danaher Corporation (Sunnyvale, CA)
    …(IVDR) as well as other applicable global regulatory requirements, including Medical Device Single Audit Program (MDSAP) participating regulatory authorities ... Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Senior Quality Systems Specialist is responsible for functioning as Lead… more
    Danaher Corporation (08/16/25)
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  • Product Quality Assurance Analyst III

    Abbott (Alameda, CA)
    medical devices, customer complaints, and product nonconformances. Prior experience in the medical device industry and/ or quality systems are required. ... colleagues serve people in more than 160 countries. **Product Quality Analyst III** **Working at Abbott** At Abbott, you... Code of Federal Regulations as it applies to medical device manufacturing, including cGMP, ISO14971, as… more
    Abbott (08/08/25)
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  • Staff Quality Engineer

    Stryker (Irvine, CA)
    …**Preferred:** + MS, CQE, or CRE. + Six Sigma Green or Black belt. + Medical device industry experience is strongly preferred. + Experience in interacting with ... Stryker - Inari Medical (https://www.inarimedical.com/) is hiring a **Staff Quality...MoH, TUV, etc.). + Understanding of US and International Medical Device Regulations. + Familiarity with ISO… more
    Stryker (08/09/25)
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  • Quality Inspector

    Abbott (Santa Clara, CA)
    …work efficiently under tight timelines. **Preferred** + 5+ years prior medical device experience preferred. Apply Now (https://www.jobs.abbott/us/en) **Learn ... Our business purpose is to restore health and improve quality of life by designing and providing device...of employees, customers, contractors, and vendors. + Knowledge of Quality Systems, FDA regulations, ISO 13485 and… more
    Abbott (07/24/25)
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  • Executive Director of R&D Global Quality

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …and Skills: **Qualifications** + Bachelor's degree and 15+ years of experience in a FDA regulated pharmaceutical and/or medical device industry environment + ... an experienced and dynamic Executive Director of R&D Global Quality to join our team. This pivotal role will...Previous experience of working in the global pharmaceutical and medical device industry. + Experience working with… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • Technician, Senior Quality Production

    Abbott (Santa Clara, CA)
    …with all levels of employees, customers, contractors, and vendors. + Knowledge of Quality Systems, FDA regulations, ISO 13485 and applicable worldwide regulator ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (07/26/25)
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  • Quality Systems Specialist III

    Danaher Corporation (Sunnyvale, CA)
    …(IVDR) as well as other applicable global regulatory requirements, including Medical Device Single Audit Program (MDSAP) participating regulatory authorities ... Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Quality Systems Specialist III is responsible for functioning as… more
    Danaher Corporation (08/26/25)
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  • Sr. R&D Engineer - Shockwave Medical

    J&J Family of Companies (Santa Clara, CA)
    Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... with the company's Design Control requirements and consistent with FDA , ISO, and MDD requirements + Prototype and develop...Biomedical/Bioengineering) with a minimum of 5 years' experience in medical device engineering or a master's degree… more
    J&J Family of Companies (08/13/25)
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  • Sr Quality Manager, Failure Analysis

    BD (Becton, Dickinson and Company) (Irvine, CA)
    …methodologies + Quality Engineering, Quality Management, R&D within the medical device industry + Demonstrated track record in management of technical ... Become a **maker of possible** with us. The Senior Quality Manager, Failure Analysis will lead a team of...+ Bachelor's Degree in engineering and 8+ years of medical device industry experience including: + Failure… more
    BD (Becton, Dickinson and Company) (08/24/25)
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