This position can be filled anywhere in the United States. Candidate is not required to live in California I. Job Overview: The Regulatory Affairs Associate Director is an individual contributor that leads, plans, coordinates, conducts, and reports on in vitro diagnostics and medical device projects and programs both. Manages regulatory agency authorizations, approvals, registrations, and licensure documentation for submissions both in the US and internationally. Executes department and cross-functional projects; identifies regulatory operations activities for project schedules; serves as a core team member and core team leader; and recommends appropriate actions on regulatory and compliance issues. Provides regulatory advice, analys
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