Regulatory Affairs Senior Supervisor

About the role

The Global Regulatory Affairs Senior Supervisor will ensure that our pharmaceutical products meet all regulatory requirements across regions. You will support the preparation and submission of regulatory dossiers, maintain accurate documentation, and collaborate with cross‑functional teams to address compliance issues.

Key responsibilities

• Assist in preparing and submitting regulatory dossiers for product registrations and approvals.
• Maintain up‑to‑date regulatory documentation and records.
• Support regulatory compliance with local and international standards.
• Provide regulatory guidance to cross‑functional teams.
• Help prepare for and manage audits and inspections.
• Ensure labeling and packaging meet regulatory requirements.
• Contribute to the development of regulatory strategies for product launches.

Required profile

• Minimum 6 years of experience in regional and global pharmaceutical regulatory affairs.
• Master’s degree or professional certificate in a relevant field.
• Strong knowledge of changing regulatory requirements and industry guidelines.
• Excellent communication, ownership, and collaborative skills.

Required skills

What we offer

• Opportunity to work on global product launches.
• Collaborative environment with cross‑functional teams.
• Professional development and training.