Explore your potential as a Senior Regulatory Affairs Consultant focusing on licensing compliance in the pharmaceutical field. This contract role combines strategic project management with regulatory expertise. Reporting to the Manager of Regulatory Services, you will oversee the management of Drug Establishment Licences (DEL) and related facilities.

Your expertise will be critical for timely submissions and maintaining strong relationships with Health Canada and other regulatory entities. Engage with cross-functional teams to ensure compliance and effective project execution. Key Responsibilities:

- Lead the management of Facility Licences including MDEL
- Coordinate the submission of regulatory documents and amendments




- Identify gaps and ensure regulatory compliance
- Facilitate GMP audits and respond to Health Canada inquiries
- Monitor changes in regulations and communicate updates Requirements:
- Bachelor’s degree in Science required
- 3-5 years experience in regulatory affairs
- In-depth knowledge of Health Canada regulations
- Robust organizational and project management abilities
- Excellent communication for stakeholder engagement Utilize your regulatory skills to drive compliance and enhance client operations in healthcare.

📌 Senior Regulatory Affairs Consultant Position (Mississauga)
🏢 Q C
📍 Mississauga