dekaRichmond, NH
Regulatory Strategy Lead — Medical Devices & FDA Approvals
Regulatory Strategy Lead — Medical Devices & FDA Approvals
Regulatory Strategy Lead — Medical Devices & FDA Approvals
dekaRichmond, NH
yesterday
Electromedical and Electrotherapeutic Apparatus ManufacturingSurgical and Medical Instrument ManufacturingSurgical Appliance and Supplies Manufacturing
Apply for this role →DEKA Research & Development is seeking a Regulatory Affairs Project Manager to shape regulatory strategies for FDA clearance/approval and international approvals including CE Marking. You will work closely with development teams and customers to drive 510(k)s, PMAs, IDEs and technical files, while guiding R&D on regulatory paths across the product life cycle.
The role requires strong communication, 5+ years in regulated life sciences, and experience with FDA processes such as Q-submissions and
Also on the board Same function, level within a rung
Level
Manager
Location
Richmond, NH
Occupation
Regulatory Affairs Managers
Industry
Electromedical and Electrotherapeutic Apparatus Manufacturing
Posted
yesterday