We are partnered with a leading Medical Device company focused in a range of Class II-III Devices! They have industry leading products throughout the US and Internationally.
The Global Regulatory Affairs Director will lead a Regulatory unit having responsibility for obtaining and maintaining product approvals with a range of Class II-III Devices and is responsible for driving cross-functional teams in preparing regulatory dossiers for submission to the FDA and other global health authorities.
If you have the below skillset, please reach out!
12+ years of regulatory experience with medical devices
Led/Authored 510K / PMA / MDR / International submissions
Class II-III Product Experience
Experience leading Direct Reports/ Managing Regulatory Units
Seniority level
Director
Employment type
Full-time
Job function
Management, Product Management, and Strategy/Planning
Industries
Medical Equipment Manufacturing
Referrals increase your chances of interviewing at Discover International by 2x