• Associate Staff Engineer - Sustaining

    BD (Becton, Dickinson and Company) (Salt Lake City, UT)
    …milestones on time and within budget. The ideal candidate should have experience in medical device industry or related field. Knowledge of FDA regulations, IEC ... **Job Description Summary** Associate Staff Engineer - Sustaining **Job Description** We are **the...or Science discipline plus 6 years relevant experience. + Medical device industry experience preferred. + Ability… more
    BD (Becton, Dickinson and Company) (10/22/25)
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  • Sr Product Development Engineer (E4)

    Zimmer Biomet (Englewood, CO)
    …or related engineering discipline with 6+ years of experience + Prior experience in medical device development required. + Prior experience in taking a ... belonging. **What You Can Expect** The Sr. Product Development Engineer leads the design of new products and improvements...medical device or similar product from ideation… more
    Zimmer Biomet (11/04/25)
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  • Principal Systems Engineer , R&D - BD…

    BD (Becton, Dickinson and Company) (Irvine, CA)
    …engineering (MedTech industry preferred) + Consistent track record of leading complex medical device development from concept to market + Strong knowledge ... of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products...of regulatory requirements and quality standards in the medical device industry (FDA, ISO 13485, ISO… more
    BD (Becton, Dickinson and Company) (11/23/25)
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  • Senior Engineer , Sustaining

    BD (Becton, Dickinson and Company) (Vernon Hills, IL)
    …+ Minimum 5 years in product and process engineering within the ** medical device ** or **pharmaceutical** industry. + Proven experience in **project ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products… more
    BD (Becton, Dickinson and Company) (11/23/25)
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  • Senior Process Engineer

    Stryker (Mahwah, NJ)
    …want:** The MIM Engineer will lead technical efforts to introduce new medical device products using Metal Injection Molding (MIM) technology and ensure ... to deliver robust, compliant, and cost-effective processes that meet stringent medical device standards and high-volume output requirements. **Key… more
    Stryker (12/09/25)
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  • Quality Engineer

    Actalent (Watertown, CT)
    …Responsibilities + Ensure that all testing processes and product developments comply with relevant medical device regulations such as FDA (21 CFR Part 820) and ... Job Title: Quality Engineer For immediate consideration, please email resume to...risk assessments to identify potential hazards associated with the medical device and develop mitigation strategies. +… more
    Actalent (12/04/25)
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  • Engineer II, R&D

    Terumo Neuro (Aliso Viejo, CA)
    …prepare technical documentation. 4. Knowledge of standard machine shop equipment, processes, and medical device manufacturing equipment. 5. Knowledge of ... Engineer II, R&D **Job Description:** Support development of medical device products with work including writing...or rotation program preferred. 8. One (1) year of Manufacturing experience preferred. **EEO** We are an equal employment… more
    Terumo Neuro (12/03/25)
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  • Project Engineer

    Globus Medical, Inc. (Audubon, PA)
    …The Project Engineer will offer technical support for the advancement of medical device and biologic products. This role entails conducting research and ... CBER, and CDRH regulatory requirements + Hands-on experience in process development, manufacturing , or quality systems for medical devices, biologics or… more
    Globus Medical, Inc. (11/06/25)
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  • Automation Machine Vision Engineer

    DEKA Research & Development (Manchester, NH)
    … to join our industrial automation team developing vision inspection systems for medical device manufacturing . This role will collaborate with both ... Clear technical documentation and communication skills Preferred Qualifications: + FDA-regulated medical device manufacturing experience + Statistical… more
    DEKA Research & Development (10/25/25)
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  • Quality Engineer I

    Tecomet (Claypool, IN)
    …Preferred:** + ASQ CQE or CMQ/QE preferred + 2 years' experience in quality within medical device manufacturing industry preferred + ISO 13485, FDA 820 and ... or related field. Or a minimum of 4 years' experience within the Medical Device Industry, and Certification (ASQ CQE or CMQ/QE) **Experience/Educational/Training… more
    Tecomet (11/19/25)
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