applicants

Staffing companies and 3rd party companies do not repond to this ad*

QA Compliance Manager:
Quality and Regulatory affairs medical device experience as well as experience with ISO 13485 certified quality systems and FDA Quality System Regulation compliance is required.

This is a temp to perm position located on site in Westerly, RI.

FDA regulatory experience required
quality systems experience required

Candidate will manage the product quality of the product line
temp to perm opportunity