Latest Medical Device Regulatory Affairs jobs in Fremont, CA

27 Medical Device Regulatory Affairs Jobs in Fremont, CA

Graphic Illustrator ATR International - Fremont, CA, United States documentation for clarity and accuracy without changing key information; • Work with Sales & Marketing and Regulatory Affairs departments to determine requirements and attend meetings. Requirements: • 3 - year 18 days ago
Regulatory Affairs Manager EPM Scientific - San Jose, CA, United States Title: Regulatory Affairs Manager Location: San Jose, CA Base Salary: $140,000-$190,000 About: Currently working with a medical device company dedicated to developing and commercializing breakthrough 7 days ago
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 28 days ago
Associate Quality Engineer Bayside Solutions - Santa Clara, CA, United States in conjunction with Regulatory Affairs. Investigate and review medical device complaints to help identify root causes, solutions, and trends. Perform risk assessments. Write protocols and reports for activities 9 days ago
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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 18 days ago
Regulatory Specialist II The Fountain Group LLC - Alameda, California + years of regulatory affairs experience Medical Device regulatory affairs experience Job Description: Responsible for regulatory activities, including product registrations, impact assessment, etc 3 days ago
Regulatory Specialist GForce Life Sciences - Alameda, CA, United States Regulatory Affairs Specialist II – On-site in Alameda, CA Qualifications BS in Life Sciences or Medical Engineering/Technology 5+ years of professional experience (not internship experience) Medical 9 days ago
Regulatory Affairs Specialist GForce Life Sciences - Santa Clara, CA, United States of regulatory strategy and priorities in conjunction with management, peers, and commercial, and affiliate personnel in the medical device industry. Key Responsibilities: Duties: Assist in the definition 27 days ago
Principal Regulatory Affairs Specialist – Heart Failure (on-site) Abbott Laboratories - Pleasanton, California with Class II and/or Class III medical devices. Regulatory Affairs Certification (RAC) is a plus. Experience with either 510(k) applications, PMA supplements and US device regulations, or with EU and other 4 days ago
Regulatory Affairs Specialist II – Heart Failure Abbott Laboratories - Pleasanton, California enterprise/cross-division business unit model. Experience working in the Medical Device industry. Regulatory Affairs Professionals Society Certification is a plus. * Participants who complete a short wellness 4 days ago

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