My client, a global medical device company located in the Bay Area is looking for an experienced Regulatory Affairs professional to join their team. They are offering a rare opportunity to join a collaborative team working on next generation products with a lucrative base + benefits.
-Directly aid in development and implementation of Regulatory strategy, both domestic and international
-Manage the development and assure time-line of new devices/products pathway to clearance
-Work closely with R&D and engineering teams to guarantee requirements are understood and met
-Lead submissions and participate in audits as required
-Bachelor's degree in related field
-Master's degree (PhD. preferred)
-7+ years Regulatory Affairs experience (Medical Device/CMC)
Sthree US is acting as an Employment Agency in relation to this vacancy.