Pharmaceutical Affairs Lead, Benelux

beonemedicines.ar

Regulatory affairs expertise
Pharmacovigilance experience
Oncology market knowledge
The Pharmaceutical Affairs Lead will oversee regulatory compliance and quality assurance in Belgium and Luxembourg

Job Summary

  • The Pharmaceutical Affairs Lead will oversee regulatory compliance and quality assurance in Belgium and Luxembourg.
  • This role involves acting as a Qualified Person Responsible for Information and Publicity and managing medical information.
  • Candidates should have a strong background in the pharmaceutical industry with a focus on oncology.

Matching Summary

The Pharmaceutical Affairs Lead will oversee regulatory compliance and quality assurance in Belgium and Luxembourg.

Skills & Requirements

Must-have

  • Regulatory affairs expertise
  • Pharmacovigilance experience
  • Oncology market knowledge

Nice-to-have

  • Trilingual communication skills
  • Dynamic work environment
  • Cross-functional collaboration

Key Requirements

  • Minimum 10 years in regulatory affairs
  • Certified Prevention Adviser Level III
  • Fluent in English, French or Dutch

Work Rights

Not specified

Tailored Resume

Cover Letter