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Post-Market Regulatory Manager II

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Bedford, United States Werfen North America Full time

A leading medical device company in Bedford, Massachusetts, is seeking a Regulatory Affairs Manager II to oversee regulatory compliance for post-market medical devices. The role involves leading a team, ensuring adherence to FDA and international regulations, and developing processes for vigilance reporting and product changes. Required qualifications include a Bachelor’s degree and at least 5 years of management experience in the medical device field. The position offers a competitive salary between $160K and $190K plus an annual bonus.#J-18808-Ljbffr