Regulatory Affairs Consultant - Medical Devices | Interim (until end of 2026)

Excellence Squad is a European consulting firm specializing in Operational Excellence, Quality & Compliance, and Project Leadership across industries. We help organizations achieve measurable results through structured execution and performance excellence. Our client, a leading medical device company based in Belgium, is looking for an experienced Regulatory Affairs Consultant to join their team on an interim basis until the end of the year. Your Role As Regulatory Affairs Consultant, you will: Develop regulatory strategy and create detailed regulatory plans Review development quality reports and plans to ensure information required for regulatory submissions and product compliance is adequate Plan, generate, and coordinate regulatory submissions for product certification and approvals Coordinate conformity assessment strategies and plans required to support regulatory submissions Review and approve product labeling and product-related marketing communications Maintain existing regulatory filings and licenses, managing updates and related change control