Regulatory Affairs Specialist - Medical Devices - EN
Company: MICHAEL PAGE INTERNATIONAL (BELGIUM) Agency
- Location: Belgium
- Seniority: Entry level
- Employment type: Full-time
- Posted: Yesterday
- Offer language: English
Job description
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
As a successful Regulatory Affairs Specialist - Medical Devices - EN, you will have the following profile:
- Bachelor's degree in Life Sciences, Biomedical Sciences, Pharmacy, Regulatory Affairs or related field
- 1-3 years of experience in Regulatory Affairs within medical devices
- Strong knowledge of MDR requirements and registration processes
- Experience supporting product registrations and lifecycle activities
- Excellent communication and stakeholder management skills
- Proactive personality who actively seeks information and drives actions forward
- Comfortable collaborating with international stakeholders
- Fluent in English
- Strong analytical and organizational skills
- Team-oriented with a continuous improvement mindset
