Staffmark Group
Regulatory Affairs Pro – FDA/Medical Devices
Staffmark Group, Torrance, California, United States, 90504
A consulting firm in Torrance is seeking a Regulatory Affairs Specialist who excels in managing FDA compliance submissions. The role involves high-level coordination with regulatory bodies, strategic research, and providing detailed reports. Candidates should have a Bachelor’s degree in a STEM field and experience in the medical device or pharmaceutical sector. This position offers flexibility in schedule and a team-oriented culture, alongside competitive salary and benefits.
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