About this opportunity
DEKA Research and Development lists this Regulatory Affairs PM - Medical Devices Strategy opportunity in manchester, New Hampshire. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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.
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Worksite address
manchester, NH, 03103, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.