DEKA Research and Development is seeking a Regulatory Affairs Project Manager to lead regulatory strategy for medical device programs. You will define requirements, prepare submissions, and guide cross‑functional teams to approvals and clearances.
You will interact with the FDA and international regulators, mentor staff, and continuously improve regulatory processes to shorten time to market while maintaining compliance.
#J-18808-LjbffrRegulatory Affairs PM - Medical Devices Strategy in manchester at Unknown Company
This position is listed as full time and onsite.