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Regulatory affairs consultant - medical devices | interim (until end of 2026)

Anvers
Intérim
Vi-Jo - Enlightened Consulting
Médical
De 80 000 € à 100 000 € par an
Publiée le 28 avril
Description de l'offre

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.

You can get further details about the nature of this opening, and what is expected from applicants, by reading the below.

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

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

Your Profile
You have a solid track record in Regulatory Affairs within the medical device industry, with strong knowledge of EU MDR and conformity assessment processes. You are hands‑on, well‑organized, and able to work independently in a dynamic environment. Fluency in English is required; additional European languages are a plus.

Why Join

Contribute to a strategically important project within a leading medical device company in Europe

Work in a multicultural, performance‑oriented, and compliance‑driven environment

Apply your Regulatory Affairs expertise in a complex, high‑impact setting

Flexible freelance conditions within a professional consulting framework

What's On Offer
A full‑time interim assignment (flexibility possible) with a well‑established international medical device company in Belgium.

EEO Statement
At Excellence Squad, we welcome applications from all qualified individuals regardless of race, ethnicity, gender, sexual orientation, religion, or disability status. xphnsxz We do not accept inquiries from recruitment, staffing, or advertising companies.

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Accueil > Emploi > Emploi Santé > Emploi Médical > Emploi Médical à Anvers > Regulatory Affairs Consultant - Medical Devices | Interim (until end of 2026)

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