Regulatory Affairs Specialist - Medical Devices - EN

Jobat; Vlaams-Brabant; Presencial; EUR 60 000 - 85 000; Tempo integral

Resumo da oferta

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

Responsabilidades

• 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

Descrição da oferta de emprego

International healthcare organization active in the medical device sector, supporting patient care through innovative products distributed across multiple global markets.

Jobomschrijving

As a successful Regulatory Affairs Specialist - Medical Devices - EN, you will have the following 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