Medical Device Regulatory Affairs Specialist - Onsite (Torrance)
Actalent
Actalent is seeking a Regulatory Affairs Specialist to support medical device compliance activities, regulatory documentation, and quality system requirements in Torrance, CA. This role covers Class I and II programs, including design history files, change control, risk management, labeling reviews, and audit readiness. The ideal candidate will have FDA-regulated/ISO 13485 experience, Class I device focus, and strong cross-functional collaboration skills in a fast-paced manufacturing environment. #J-18808-Ljbffr Actalent
Vacancy posted 2 days ago
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