General information
            
            
                
                
                
                
        
                
                
                    
                        Publication date
                    
                    20/08/2025
                
                
                
             Position description
	Category
OPERATIONS - ENGINEERING/PRODUCTION
	Job title
Junior regulatory affairs specialist - Life Sciences - M/V/X
	Contract
Permanent contract
	Job description
	Context
The Nominated Signatory (NS) team ensures that all scientific and promotional communications to healthcare professionals (HCPs) comply with Belgian and Luxembourg pharmaceutical legislation and ethical codes. They also manage quality systems for medicine samples and ensure transparent reporting of transfers of value to HCPs and healthcare organizations.
Key Responsibilities
Support the Nominated Signatory in:
- Pre-approving promotional and non-promotional materials
- Overseeing events (promotional meetings, advisory boards, etc.) and service fees to consultants
- Managing sponsorships/donations to HCOs and patient   organizations
- Reviewing scientific leaflets and coordinating with Regulatory Affairs
- Submitting data on transfers of value to authorities (FAMHP, Betransparent.be)
Use tools like:
- Microsoft Office
- Veeva CRM & Vault Promomats
- Internal AstraZeneca portals
- Mdeon portal
 
 
Internal & External Stakeholders
Internal: NS Team, Brand Managers, Commercial/Medical/Regulatory Affairs teams, Compliance Manager, Management
External: MDEON, Pharma.be, Betransparent.be, Key External Experts (KEEs)
 
	Business Industry
Life sciences
	Profile
	Education & Qualifications
Required:
Master’s degree (preferably in pharmaceutical care or development)
Solid understanding of promotional regulations and ethical codes
Knowledge of medicine marketing and commercialization
Proficient in Dutch, English, and French
Excellent MS Office skills
 
Skills & Experience
Required:
Quick learner
Team player
Minimum 2 years’ experience in pharmaceutical/medical device industry (RA, medical, or clinical development)
Administrative experience
Strong communication skills
Preferred:
Prior experience in a pharmaceutical office-based admin role
Experience in RIP or Compliance
 
 
 
 Position location
	Job location
Europe, Belgium, Flanders
	Location
	Noordkustlaan 17B Dilbeek
Candidate criteria
	Level of experience
1 to 3 years