Junior regulatory affairs specialist - Life Sciences - M/V/X

Vacancy details

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