- ThermoFisher Scientific (West Hills, CA)
- …Abilities** + Detailed knowledge of ISO and GMP regulations which govern a medical device and diagnostics manufacturing. + Familiarity of statistical process ... Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** The Engineer II, Quality is responsible for creating...count on, which includes: + A choice of national medical and dental plans, and a national vision plan,… more
- Medtronic (Northridge, CA)
- …management framework, ensuring compliance with ISO 10993 standards and global medical device regulations. This role involves conducting comprehensive ... world. **A Day in the Life** The Senior Product Engineer is responsible for leading biological evaluations within a...preferred. + Strong understanding of ISO 10993 and global medical device regulations (eg, EU MDR, FDA,… more
- Abbott (Temecula, CA)
- …diversity, working mothers, female executives, and scientists. **The Opportunity** **The Sr, Quality Engineer position works onsite of our Temecula, CA location ... writing skills. **Preferred Qualifications** + Masters Degree Preferred + Prior medical device experience preferred. ASQ CQE certification preferred. Design… more
- Cisco (San Jose, CA)
- …hiring process. US employees haveaccess (https://www.cisco.com/c/en/us/about/careers/we-are-cisco/benefits-and-perks.html) to quality medical , dental and vision ... Principal Hardware Engineer - Quality & Reliability Apply...for the semiconductor industry. + In-depth knowledge of semiconductor device & package fail mechanisms/symptoms + Multiple roles a… more
- Meta (Burlingame, CA)
- … medical devices compliance team, focusing on wearables and Software as a Medical Device (SaMD). This role will be responsible for developing, implementing, ... technical field, or equivalent practical experience 7. 5+ years of experience in medical device system engineering or a related role 8. Understanding and… more
- Abbott (Alameda, CA)
- …development is required. **Preferred Qualifications** + Solid knowledge of regulations for medical device development, (EN460001, ISO13485, FDA) is desirable. + ... preferred + Embedded UI design experience preferred + Detailed experience with medical device development processes and FDA 510K and PMA regulatory requirement… more
- BD (Becton, Dickinson and Company) (Irvine, CA)
- … development from concept to market + Strong knowledge of regulatory requirements and quality standards in the medical device industry (FDA, ISO 13485, ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...are committed to improving patient outcomes and enhancing the quality of life through our advanced hemodynamic monitoring solutions.… more
- 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 ... Johnson & Johnson is hiring for a **Principal R&D Engineer (Balloon Technology) - Shockwave Medical ** to...relevant engineering/technical degree and 10 years' experience in the medical device industry or a Master's Degree… more
- Caldera Medical (Westlake Village, CA)
- …is Caldera Medical ? Caldera Medical is a growth stage medical device company dedicated to improving the quality of life for women. In 2018, Caldera ... California Sponsorship is not available for this role. Caldera Medical 's Mission - To Improve the Quality ...for Women! Message from the Hiring Manager: The Supplier Engineer is a key member of Caldera Medical… more
- Teleflex (Pleasanton, CA)
- …from objectives * Proven problem solving and trouble shooting skills * Experience with quality management systems and medical device regulations * Proven ... Sustaining Engineer III **Date:** Aug 10, 2025 **Location:** Pleasanton,...working in a new product development, sustaining engineering in medical device industry or at least 3… more