Global Medical Devices Regulatory Affairs Specialist

Michael Page (Belgium); Vlaams-Brabant; On-site; EUR 52,000 - 70,000; Full time

Benefits offered by this job

Permanent contract

Salary package

Benefits

Job summary

Michael Page Belgium is seeking a Regulatory Affairs Specialist for the medical devices sector to coordinate registrations across international markets and ensure MDR compliance. You will prepare and submit regulatory documentation, support lifecycle changes, and liaise with manufacturers, distributors and authorities.

The role requires a Life Sciences or regulatory-focused degree, 1–3 years of Regulatory Affairs experience in medical devices, and fluent English.

Qualifications

• Bachelor's or master's degree in Life Sciences or regulatory field.
• 1–3 years of Regulatory Affairs experience in medical devices.
• Good knowledge of MDR and regulatory documentation.
• Proactive, organized, with strong communication skills.
• Experience working with international teams.

Responsibilities

• Coordinate medical device registrations across markets.
• Prepare, review, and submit regulatory documentation with stakeholders.
• Support regulatory compliance and lifecycle changes.
• Review marketing materials for regulatory impact.
• Monitor regulatory developments and communicate updates.
• Act as contact for manufacturers, distributors and authorities.

Skills

Regulatory affairs

MDR knowledge

Product registrations

Lifecycle management

Change control

Regulatory intelligence

Regulatory documentation

Stakeholder communication

English fluent

Education

Bachelor's or Master's in Life Sciences / Regulatory Affairs

Regulatory affairs related degree or certification

Job description

Michael Page Belgium is seeking a Regulatory Affairs Specialist for the medical devices sector to coordinate registrations across international markets and ensure MDR compliance. You will prepare and submit regulatory documentation, support lifecycle changes, and liaise with manufacturers, distributors and authorities.

The role requires a Life Sciences or regulatory-focused degree, 1–3 years of Regulatory Affairs experience in medical devices, and fluent English.