Medical Device Regulatory Affairs Jobs in Fremont, CA

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

from: linkedin.com - 18 days ago

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

from: linkedin.com - 7 days ago

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

from: Pharmadiversityjobboard.com - 28 days ago

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

from: linkedin.com - 9 days ago

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

from: linkedin.com - 18 days ago

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

from: resume-library.com - 3 days ago

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

from: linkedin.com - 9 days ago

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

from: linkedin.com - 27 days ago

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

from: resume-library.com - 4 days ago

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

from: resume-library.com - 4 days ago