• Senior Program Manager - Development Process…

    Medtronic (Northridge, CA)
    …Technical degree is a plus. + Experience with Design Control documentation within medical device industry or Pharma industry. + Experience conducting and ... of initiative and self-motivation. + Prior work experience in a regulated industry ( Medical Device Industry preferred) + Sound experience and through knowledge… more
    Medtronic (09/04/25)
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  • R&D Fellow, Systems Engineering, Interventional…

    Philips (San Diego, CA)
    …solutions through product development, integration and V&V, ensuring compliance with medical device standards and global regulatory requirements. ... and thorough manner. + You have experience working in the regulated medical device environment: demonstrating practical knowledge and experience with global… more
    Philips (08/21/25)
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  • Director of API Manufacturing

    Kelly Services (South San Francisco, CA)
    …advance your career, join us as we pioneer progress in the biotechnology and medical device industries. **Workplace:** Hybrid, onsite in South San Francisco, CA, ... of CMC, you'll be instrumental in overseeing API process scale-up, regulatory strategy, and operational excellence required for clinical and commercial success.… more
    Kelly Services (08/29/25)
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  • Chief Litigation Officer - Diabetes

    Medtronic (Los Angeles, CA)
    …legal counsel, and protect the company's rights and reputation in a highly regulated medical device industry. The Chief Litigation Officer will play a pivotal ... + Significant experience with product liability and intellectual property litigation within the medical device or healthcare industry. + Proven ability to lead… more
    Medtronic (09/03/25)
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  • Sr R&D Process Engineer

    Medtronic (San Diego, CA)
    …Diabetes Business Unit. The ideal candidate for this position has experience in medical device design and process development, and characterization testing. This ... + Develop and validate test methods and inspection methods. + Understanding of medical device design control process; lead design reviews and ensure on-time… more
    Medtronic (09/03/25)
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  • CSV Automation Specialist

    VTI Life Sciences (San Diego, CA)
    …engineers looking to accelerate their career in the pharmaceutical, biotechnology and medical device industries. We offer an opportunity to help support ... Automation and Validation Services to the Pharmaceutical, Biotechnology, Biologics and Medical Device industries. VTI offers professional development, training,… more
    VTI Life Sciences (08/13/25)
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  • Account Director/ Sr Account Director Business…

    ThermoFisher Scientific (Carlsbad, CA)
    …organizational expertise, and **_deep industry knowledge across the pharmaceutical, biotech, or medical device sectors_** , along with a proven track record ... key account management in a related Pharmaceutical, Biotech or Medical Device sales industry + Experience in...common customer needs in this field. + Awareness of regulatory landscape, including understanding regulatory bodies, compliance… more
    ThermoFisher Scientific (07/03/25)
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  • Director R&D Program Management

    Abbott (Pleasanton, CA)
    …levels in the organization. + Minimum of ten (10) years' experience in medical device development and/or other highly regulated industry + Previous experience ... work closely with cross-functional peers in quality, operation, marketing, clinical and regulatory , medical affairs, commercials to define an aligned and… more
    Abbott (08/13/25)
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  • Staff R&D Engineer

    Imperative Care (Campbell, CA)
    …discipline and a minimum of 8 years of related experience developing flexible medical device instruments; or equivalent combination of education and work ... experience in related regulated industry. + MS in Engineering and experience in medical device development in a start-up environment preferred. + Statistical… more
    Imperative Care (08/01/25)
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  • Quality Engineer, Design Control

    Hologic (San Diego, CA)
    …environment, ideally in the IVD space. + Working knowledge of Quality Management System for Medical Device Manufacturing FDA 21 CFR 820, ISO 13485 as well as CE ... mark requirements, In Vitro Diagnostic Regulation (EU) 2017/746 and Medical Device Regulation (EU) 2017/745, Risk Management ISO 14971, and other applicable… more
    Hologic (07/03/25)
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