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Regulatory Affairs Sr Specialist

Minnetonka, Minnesota, United StatesExternalPosted Oct 1, 2026

Job description

Exciting opportunity for a Regulatory Affairs Sr Specialist to support regulatory submissions and provide regulatory direction for medical devices.

Key responsibilities include

authoring submissions and advising development teams. Ideal for candidates with advanced regulatory knowledge and significant experience in medical device or engineering fields.

Description copied from Zimmer Biomet Holdings's careers page. Read the full posting before you apply.

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