Global Regulatory Affairs Expert, Medical Devices

A leading regulatory consulting firm in Bedford, MA is seeking a Regulatory Affairs Specialist to ensure compliance for Class II medical devices. Responsibilities include determining assessments, preparing submissions, and supporting product registrations. Candidates should possess a Bachelor’s in life sciences and at least 3 years of relevant experience in the medical device field, along with strong communication skills.

This role offers a hybrid work setting with opportunities for growth and professional development.
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