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.