• Tools for Humanity (San Francisco, CA)
    …supporting the Worldcoin open-source protocol by managing Tools for Humanity's legal affairs globally. We collaborate across the company to advance the blockchain ... and enhance our products, including the Orb (our hardware device ), World ID, World App, and World Chain. We...with the Worldcoin Foundation and other partners to ensure regulatory compliance in areas such as securities, AML/CFT, consumer… more
    Upward (08/11/25)
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  • Programmable Medicine Operatin (Redwood City, CA)
    …meetings with Clinical Operations, Clinical, Clinical Supply Chian, Quality Assurance, and Regulatory Affairs Responsible for drug substance and drug product and ... on developing novel nanomedicines, HD therapeutics (HDTs), to treat unmet medical needs in ophthalmology, neurology, inflammatory diseases, and neuro-oncology. Our… more
    Upward (08/05/25)
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  • JENAVALVE TECHNOLOGY INC (Irvine, CA)
    …knowledge of GCPs governing the conduct of clinical trials; working knowledge of Medical Device Directive 93/42/EEC, ISO14155 and ICH guidelines. Very organized ... Senior Associate, Clinical Research Supervisor/Manager Title: Senior Manager, Clinical Affairs Job Description Summary: The Senior Clinical Research Associate will… more
    Upward (08/02/25)
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  • Medical Device Regulatory

    Abbott (Santa Clara, CA)
    …executives, and scientists. **The Opportunity** We currently have several opportunities for the ** Medical Device Regulatory Affairs Development (RAD) ... to various international affiliates. + Maintains pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… more
    Abbott (09/06/25)
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  • Senior Regulatory Affairs Specialist

    Medtronic (Irvine, CA)
    Medical Device Experience:** Minimum of 4 years of relevant experience in medical device regulatory affairs . + **510(k) Submission Experience:** ... or university required; advanced degree with a minimum of 2 years of experience in medical device regulatory affairs is a plus. + ** Regulatory more
    Medtronic (09/30/25)
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  • Medical Devices, Regulatory

    Meta (Burlingame, CA)
    …a scientific discipline or equivalent work experience 6. 3+ years of industry experience in medical device regulatory affairs or related industry 7. ... **Summary:** We're seeking a regulatory affairs specialist to join our medical ...get to work on wearables and Software as a Medical Device (SaMD) applications for the US… more
    Meta (10/08/25)
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  • Regulatory Affairs Specialist

    Stryker (Fremont, CA)
    …with a solid understanding of regulatory standards and practices. + Exposure to Medical Device Regulatory Affairs or Engineering through coursework, ... Fremont, CA or Salt Lake City, Utah as a Regulatory Affairs Specialist.** At Stryker, we're driven...experience working with US Class II and Class III medical devices. + Demonstrates strong analytical and writing skills,… more
    Stryker (10/09/25)
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  • Sr. Regulatory Affairs Specialist

    Caldera Medical (Westlake Village, CA)
    …Sciences, Biomedical Engineering, or a related field. * 5-7 years of regulatory affairs experience in the medical device industry. * Strong understanding ... Sr. Regulatory Affairs Specialist 100% ONSITE in... Regulatory specialist, you will develop and implement medical device regulatory strategies to… more
    Caldera Medical (08/24/25)
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  • Sr. Regulatory Affairs Specialist-…

    Medtronic (Los Angeles, CA)
    …healthcare, or regulatory -related field and 4+ years of regulatory affairs experience, preferably with medical device submissions, registrations or ... -related field and 2+ years of regulatory affairs experience, preferably with medical device submissions, registrations or advertising and promotional… more
    Medtronic (10/04/25)
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  • Principal Regulatory Affairs

    Abbott (Alameda, CA)
    …working mothers, female executives, and scientists. **The Opportunity** This **Principal Regulatory Affairs Specialist - APAC** position will work on-site ... glucose levels with our new sensing technology. This **Principal Regulatory Affairs Specialist** position is responsible for...Scientific writing experience. + Solid understanding of the EU Medical Device Regulation (MDR - Regulation (EU)… more
    Abbott (10/03/25)
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  • Principal Regulatory Affairs

    Medtronic (Santa Rosa, CA)
    …with an advanced degree) **NICE TO HAVE** (Preferred Qualifications) + Regulatory Affairs experience within the medical device industry. + Strong program ... is open to US-based Medtronic facilities. The Medtronic Global Regulatory Affairs team is seeking a highly...Bachelor's degree + 7+ years of experience within the medical device industry or a regulatory more
    Medtronic (09/18/25)
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  • Sr. Regulatory Affairs Specialist

    Medtronic (Los Angeles, CA)
    …healthcare, or regulatory -related field and 4+ years of regulatory affairs experience, preferably with medical device submissions, registrations or ... -related field and 2+ years of regulatory affairs experience, preferably with medical device submissions, registrations or advertising and promotional… more
    Medtronic (10/01/25)
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  • Regulatory Affairs Manager - APAC…

    Abbott (Alameda, CA)
    …+ Work closely with in-country regulatory representatives, compile, prepare, and review medical device or IVD submissions to regulatory agencies in the ... for diversity, working mothers, female executives, and scientists. **The Opportunity** This ** Regulatory Affairs Manager - APAC** position will work on-site at… more
    Abbott (09/09/25)
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  • Regulatory Affairs Manager - Heart…

    Abbott (Pleasanton, CA)
    …mothers, female executives, and scientists **The Opportunity** We are seeking a ** Regulatory Affairs Manager** to join Abbott's Heart Failure Division on-site ... CA. As an individual contributor, the function of a Regulatory Affairs Manager is to combine knowledge... regulations and/or experience with EU and other international medical device regulations and submissions. + Ability… more
    Abbott (09/15/25)
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  • Corporate Regulatory Affairs

    Edwards Lifesciences (Irvine, CA)
    …to impact patients around the world with pioneering technology. The Corporate Regulatory Affairs Specialist position provides Regulatory support and ... leadership to Edwards Lifesciences' Corporate Regulatory Affairs team and cross-functional teams. The role provides a...For (Preferred)** : + Degree in scientific discipline + Medical Device , Pharma, or Biotechnology industry experience… more
    Edwards Lifesciences (09/25/25)
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  • Senior Regulatory Affairs Specialist…

    Abbott (Santa Clara, CA)
    …catheters and software, vessel closure devices and peripheral stents. This Senior Regulatory Affairs Specialist position is an onsite opportunity working out ... As an individual contributor, the function of a Senior Regulatory Affairs Specialist is to provide support...in a timely manner. + Experience working in the Medical Device industry. + Certification is a… more
    Abbott (07/29/25)
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  • Staff Regulatory Affairs Specialist…

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …preferred + RAPS RAC certification preferred + Minimum of 5 years of strong Regulatory Affairs /Compliance experience in medical devices + Experience with ... **Job Description Summary** As Staff Regulatory Affairs Specialist, you will be...to comply with new and existing regulations (eg, FDA Medical Device Regulations, EU-MDR) + Problem solve… more
    BD (Becton, Dickinson and Company) (08/30/25)
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  • Senior Director Regulatory Affairs

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …direct professional experience ( Regulatory ) in increasingly responsible positions in the medical device field and seven (7) years of management experience + ... possible** ! BD is one of the largest global medical technology companies in the world. _Advancing the world...a **maker of possible** with us. The Sr. Director, Regulatory Affairs is the ranking Regulatory more
    BD (Becton, Dickinson and Company) (08/28/25)
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  • Associate Principal, Regulatory

    Terumo Neuro (Aliso Viejo, CA)
    **12814BR** **Title:** Associate Principal, Regulatory Affairs **Job Description:** Responsible for establishing and preparing strategy for worldwide product ... evidence by successful US FDA Class II / III medical device submissions, EU CE Mark applications,...San Francisco Fair Chance Ordinance. **External-Facing Title:** Associate Principal, Regulatory Affairs **Posting Country:** US - United… more
    Terumo Neuro (10/09/25)
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  • Principal Regulatory Affairs

    Abbott (Alameda, CA)
    …**Qualifications** + 5 years' experience working with Class II, Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) ... US Drug regulations or with EU and other international medical device regulations and submissions. + Familiar...device regulations and submissions. + Familiar with relevant regulatory requirements for medical devices, drugs and/or… more
    Abbott (09/27/25)
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