Job title: Regulatory Affairs Officer
Job type: Contract
Emp type: Full-time
Industry: Pharmaceuticals
Functional Expertise: Pharmaceutical / CRO / Reagents / Personal Care
Skills: Danish Regulatory Affairs Dossiers Permit Reigstration Planning Registration procedure Regulatory Response to questions impact analysis Packaging material advertising material promotional material
Pay interval: Hourly
Pay rate: negotiable
Location: Belgium
Job published: 2024-02-14
Job ID: 33272
Contact name: Adam Sainter
Contact email: adam.sainter@chrlifesciences.com

Job Description

Job Title: Regulatory Affairs Officer

Location: Belgium

CHR Life Sciences are pleased to be partnering with a pharmaceutical client based in Belgium who are seeking a Regulatory Affairs Officer.

Key Responsibilities:

  • Manage registration dossier preparation and submission.
  • Coordinate permit maintenance and renewal activities.
  • Provide input on registration procedure planning.
  • Ensure compliance with national and international regulations.
  • Analyze regulatory impact of product modifications.
  • Respond to inquiries from regulatory authorities.
  • Review and approve packaging and promotional materials.

Profile:

  • Master's degree in pharmaceutical sciences or related field.
  • Extensive experience in regulatory affairs within the pharmaceutical sector.
  • Strong understanding of drug development and production processes.
  • Knowledgeable about national and international regulatory frameworks.
  • Detail-oriented with strong organizational skills.
  • Adaptable and proactive in staying updated with industry developments.
  • Proficiency in Dutch, French, and English.
  • Familiarity with Microsoft Word, Excel, and Outlook.

The role will be site based with some opportunity for hybrid working.