Regulatory Affairs Specialist

Regulatory Affairs Specialist – Medical Devices

Belgium

Permanent - Full Time

Hybrid Work - 3 days in office near Brussels

Competitive Salary + Package

Connect Life Science is partnering with a global medical device company to recruit a Regulatory Affairs Specialist for its European team.

This role offers broad international exposure, supporting market access and lifecycle management across a portfolio of medical devices and in vitro diagnostics. You’ll take ownership of registration activities across assigned territories, working closely with legal manufacturers, distributors and internal stakeholders.

The role

• Coordinate national registrations, preparing dossiers and managing submission timelines.
• Liaise with competent authorities, manufacturers and distributors to secure and maintain market authorisations.
• Assess product changes and coordinate the regulatory actions required.
• Review marketing materials and claims for regulatory compliance.
• Monitor regulatory developments and advise internal teams on their impact.
• Support improvements to regulatory processes and documentation.

Your background

• Regulatory Affairs experience within class 2 or 3 medical devices (2-5 years)
• Experience preparing registration dossiers and supporting product lifecycle management.
• Knowledge of applicable EU medical device regulations and economic operator obligations.
• Confidence working with manufacturers, distributors and cross-functional teams.
• Strong attention to detail and the ability to manage multiple registration projects.
• MDR experience and working knoweldge

Interested?

Apply with your CV or contact David Clifton at Connect Life Science for a confidential discussion.