Regulatory Affairs Consultant - Medical Devices
52729
Posted: 21/07/2026
- Antwerp, United Kingdom
- Contract
Regulatory Affairs Consultant | Medical Devices | EU MDR | Belgium | Freelance Contract
Are you an experienced Regulatory Affairs professional looking for your next contract within the medical device industry. You'll have the chance to thrive in a collaborative, high-performing environment, with the opportunity to influence regulatory strategy, drive compliance, and make a real impact. If you're looking for the ability to succeed on a high-profile project with genuine scope for development, this could be the perfect next step.
In this role, you'll take ownership of regulatory submissions and compliance activities, working closely with cross-functional teams to ensure products meet EU MDR requirements and achieve successful market approvals.
Key Responsibilities
Apply now!! Opportunities like this move quickly. If your experience matches what we're looking for, apply now and book time with me to discuss the role in more detail.
Are you an experienced Regulatory Affairs professional looking for your next contract within the medical device industry. You'll have the chance to thrive in a collaborative, high-performing environment, with the opportunity to influence regulatory strategy, drive compliance, and make a real impact. If you're looking for the ability to succeed on a high-profile project with genuine scope for development, this could be the perfect next step.
In this role, you'll take ownership of regulatory submissions and compliance activities, working closely with cross-functional teams to ensure products meet EU MDR requirements and achieve successful market approvals.
Key Responsibilities
- Develop regulatory strategies and submission plans
- Prepare and coordinate EU MDR regulatory submissions
- Support conformity assessment activities
- Review technical documentation and quality reports
- Approve product labelling and marketing materials
- Maintain regulatory licences, filings and change controls
- Proven Regulatory Affairs experience within medical devices
- Strong knowledge of EU MDR and conformity assessment
- Experience managing regulatory submissions
- Excellent organisation and stakeholder management skills
- Fluent English (additional European languages are advantageous)
Apply now!! Opportunities like this move quickly. If your experience matches what we're looking for, apply now and book time with me to discuss the role in more detail.
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