Local Regulatory Affairs Manager Benelux (Freelance/Part-time)

Freelance opportunity in Benelux! Join our global team as a Local Regulatory Affairs Manager in Belgium, Netherlands and Luxembourg. 

Local Regulatory Affairs Manager will be responsible for ensuring that medicinal and other products comply with applicable regulatory requirements by providing input and coordinating marketing authorization and post-authorization related activities. 

The position is remote (approximately 0.35 FTE) and covers the Benelux region, working in close collaboration with  the Regulatory Affairs team.  

You have energy and motivation to work in a team and to gain more experience?  

Submit your CV in the English language for consideration. 

Responsibilities: 

• Act as Local Regulatory Affairs Manager in the assigned territory.  
• Maintain timely and effective communication with local Competent Authorities.  
• Monitor and report changes in national regulatory requirements on a regular basis. 
• Develop and/or review of regulatory strategy to support product lifecycle planning, including initial market entry and post-approval changes.  
• Prepare regulatory documentation for submission to Competent Authorities. Regulatory submissions.  
• Regulatory review for labelling components (e.g., packaging, patient leaflets, SmPC), promotional materials, and product information to ensure full compliance with applicable regulatory requirements.  
• Translations.  
• Ensure accurate documentation, reporting, and follow-up of all regulatory reports.  
• Support Biomapas Clients with other RA related tasks, including strategic and operational regulatory advice.  

• Biologist, Pharmacist, Medical Doctor, or other life science degree 
• Fluent written and spoken English, German, Dutch, French and Luxembourgish 
• At least 2 years of experience in local regulatory affairs activities 
• Experience with local documents preparation and regulatory submissions  
• Excellent knowledge of local and international regulations (including knowledge concerning orphan medicinal products and the market entry aspects of centrally authorized medicines) 
• High motivation to develop and learn within the team