Latest Medical Product Specialist jobs in Sunnyvale, CA

7 Medical Product Specialist Jobs in Sunnyvale, CA

Sr. Regulatory Affairs Specialist , Medical Devices Operational Compliance Center (MD-OCC) Sunnyvale, CA , and groundbreaking devices like Fire tablets, Fire TV and Echo Frames. Working as part of the Medical Devices Operational Compliance Team (MD-OCC), the Sr. Regulatory Affairs Specialist will be working to build best 24 days ago
Regulatory Affairs Specialist GForce Life Sciences - Santa Clara, CA, United States Regulatory Affairs Specialist II – Santa Clara, CA Must be able to work on a W2 Job Summary We're looking for a Regulatory Specialist with 2-5 years of experience in the medical device industry 19 days ago
Labelling and Documentation Specialist Comrise - Fremont, CA, United States Labelling and Documentation Specialist - 12 month contract - Fremont, CA Opportunity with a leading Medical Device company As part of Sustaining R&D, the Lead Analyst, R&D Technical Writing 26 days ago
Specialist II Design Transfer at Abbott Abbott - Santa Clara, California and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. **Specialist II Design Transfer** **About Abbott** Abbott 7 days ago
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Medical Device Quality Engineer I Anatomage, Inc. - Santa Clara, California be responsible for developing and maintaining our quality system for our medical device products. Together as a team, you’ll help ensure our products are safe and follow global quality standards. This position 11 days ago
Senior Technical Publication Specialist Comrise - Fremont, CA Senior Technical Publication Specialist - long term contract Opportunity with a leading Medical Device company As part of Sustaining R&D, the Lead Analyst, R&D Technical Writing is responsible $63 - $68 29 days ago
Senior Post Market Surveillance Specialist PROCEPT BioRobotics - San Jose, California with medical affairs, customer service, global sales team, professional educators, and clinical specialists to obtain accurate complaint information. * Complete adverse event reporting determinations 20 days ago

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