- 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. ... regulatory affairs specialist to join our medical devices compliance team. You will get...get to work on wearables and Software as a Medical Device (SaMD) applications for the US… more
- Abbott (Santa Clara, CA)
- …executives, and scientists. **The Opportunity** We currently have several opportunities for the ** Medical Device Regulatory Affairs Development (RAD) ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- 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
- 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… more
- J&J Family of Companies (Irvine, CA)
- …Devices sector within **Johnson & Johnson** , is recruiting for an intern for its ** Medical Devices Regulatory Affairs organization** . At **Johnson & ... develop the skills needed to succeed in a global organization. The Intern - ** Medical Devices Regulatory Affairs (MD RA)** opportunity will help you grow… more
- Abbott (Alameda, CA)
- …+ 5 years' experience working with Class II, Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) is a plus. ... medical device regulations and submissions. + Familiar with relevant regulatory requirements for medical devices , drugs and/or biologics including… more
- Abbott (Alameda, CA)
- …. 5 years' experience working with Class II, Class III medical devices and/or biologics/drugs. Regulatory Affairs Certification (RAC) is a plus. ... regulatory submissions for Pharmaceutical, in vitro diagnostic devices and/or medical devices . ....device regulations and submissions. . Familiar with relevant regulatory requirements for medical devices … more
- Terumo Neuro (Aliso Viejo, CA)
- …assigned clinical reports, documents and scientific presentations in cooperation with the Clinical, Medical , & Regulatory Affairs Teams, KOLs and physician ... a difference in people's lives every day? We're a medical devices company that develops innovative neuroendovascular...a medical writer for pharmaceutical, CRO, or medical device clients). 4. Excellent writing and… more
- J&J Family of Companies (Irvine, CA)
- …all relevant Clinical R&D partners and cross-functional partners (eg Global Strategic Marketing, Medical Affairs , Regulatory Affairs , Health Economics ... based on study need; + In EMEA, responsible for Regulatory Affairs related tasks associated with clinical...with budget planning, tracking and control is required. + Medical Device experience is required. + Sound… more
- AbbVie (Irvine, CA)
- …to be a team leader and engage key stakeholders, including global strategic marketing, medical affairs , regulatory affairs , clinical development, and ... be to evaluate the interaction of current and future medical devices with cells and tissues for...methods to support development of novel medical device /tissue products. + Critically evaluate scientific or regulatory… more