Global Regulatory Affairs Specialist - Medical Devices

Jobat; Vlaams-Brabant; On-site; EUR 60,000 - 85,000; Full time

Job summary

Jobat is seeking a Regulatory Affairs Specialist for an international healthcare organization active in the medical device sector. You will coordinate registrations across international markets and prepare regulatory documentation with internal and external stakeholders.

You will support ongoing compliance activities, manage regulatory aspects of changes, review marketing materials for regulatory implications, monitor developments, and act as a key contact for manufacturers, distributors, and

Responsibilities

• Coordinate product registrations across assigned international markets
• Prepare and submit regulatory documentation with internal and external stakeholders
• Support ongoing compliance activities for medical device portfolios
• Manage regulatory aspects of product changes throughout the lifecycle
• Review and assess regulatory implications of marketing materials
• Monitor regulatory developments and communicate relevant updates
• Act as a key contact for manufacturers, distributors, and authorities
• Contribute to continuous improvement initiatives within Regulatory Affairs

Job description

Jobat is seeking a Regulatory Affairs Specialist for an international healthcare organization active in the medical device sector. You will coordinate registrations across international markets and prepare regulatory documentation with internal and external stakeholders.

You will support ongoing compliance activities, manage regulatory aspects of changes, review marketing materials for regulatory implications, monitor developments, and act as a key contact for manufacturers, distributors, and