Principal Regulatory Affairs Specialist - Northern California
Medical Device - Northern California
January 26, 2018
San Jose, California
110000.00 - 145000.00
Full Time - Experienced
Medical Device, Quality/Risk Management
4 Year Degree
Seeking a motivated, enthusiastic, and experienced medical device Regulatory Affairs professional. You have taken the lead on written PMA and/or 510k submissions. You have experience working cross-functionally in medical device companies. You would be excited to join a fast-paced, positive energy culture.
7+ yrs. in Regulatory Affairs ideally in Medical Device 510k or PMA submissions. You have experience driving people and projects. And, you have direct experience interacting with the FDA.
If less that 7 years, we do also have other Regulatory Affairs positions in California.
Internal Number: j2-126
About Medical Device - Northern California
Pacesetters is a medical device recruiting firm specializing in Regulatory, Clinical, and Quality. The recruiter and National Accounts Director has 20+ years niched in this space. The company attributes their success to the relationships developed with both clients and candidates--with ethics as key to all interactions.