Medical Device Regulatory Affairs Jobs in San Jose, CA

R&D Partners - San Jose, CA, United States

Regulatory Affairs, Clinical Affairs and Operations Qualifications: Bachelor’s degree in Mechanical Engineering, Electrical Engineering or relevant field 5 plus years of medical device development

from: linkedin.com - 6 days ago

TGI Life Sciences - San Jose, CA, United States

/ SKILL REQUIREMENTS Experience • Minimum 10 years of leadership experience in clinical and/or regulatory and quality in medical device and/or pharmaceutical industries. Knowledge/Skills • Working knowledge

from: linkedin.com - 24 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 - 16 days ago

Thrive - Redwood City, CA, United States

GCP Quality Assurance will provide expertise and guidance on Good Clinical Practice (GCP), applicable regulations to clinical and nonclinical...

from: linkedin.com - 3 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 - 6 days ago

Anatomage, Inc. - Santa Clara, California

We Look For Experience with Medical Device Software and Hardware Experience with QMS/eQMS Knowledge of ISO 13485 / MDSAP Global regulatory affairs experience (FDA, MDD/CE/MDR, UKCA, etc.) Document Control

from: resume-library.com (+1 source) - 2 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 - 15 days ago

Planet Pharma - Palo Alto, CA, United States

Society). Minimum of 7 years of regulatory experience within the medical device cardiovascular industry preparing Pre-submissions, PMA submissions is required. Hardware and software regulatory experience

from: linkedin.com - 12 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 - 3 days ago

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 - 6 days ago