Senior Principal Regulatory Affairs - Medical Devices

A medical device company is seeking a Senior Principal Regulatory Affairs Specialist in Saint Louis Park, MN. This hybrid role requires a minimum of 10 years of experience in Medical Device Regulatory Affairs. Responsibilities include managing regulatory strategies, ensuring compliance with FDA and international standards, and submitting regulatory filings. Ideal candidates will have strong organizational and communication skills, and a track record of success in regulatory environments.

Compensation ranges from $150,000 to $180,000 depending on experience.
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