About this opportunity
DEKA Research & Development lists this Strategic Regulatory Lead — Medical Devices opportunity in manchester, New Hampshire. Review the employer’s description below for duties, qualifications and application requirements.
Job description
A leading medical device company in Manchester, NH is seeking a Regulatory Affairs Project Manager. The role involves defining and executing regulatory strategies for FDA approval of innovative life science devices, mentoring staff, and leading FDA interactions. Candidates should have a BS in a related field and a minimum of 5 years' experience in medical device regulations. The position offers the opportunity to contribute to meaningful projects in an innovative and fast-paced environment.
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Worksite address
manchester, NH, 03103, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.