Elevate your career as a Senior Regulatory Affairs Manager at a prominent pharmaceutical manufacturer in Mississauga. Focus on Health Canada submissions with hands-on leadership to ensure strategic regulatory operations. In this pivotal role, you’ll lead the development and execution of regulatory strategies vital for product success in Canada.

A background of at least eight years in pharmaceutical regulatory affairs is required, with expertise managing Health Canada submissions and mentoring a regulatory team. This role requires guiding submission strategy, interacting with agencies, and ensuring that compliance aligns with business priorities. Key Responsibilities:

- Oversee the submission lifecycle for Health Canada
- Define and guide deficiency management strategies




- Lead agency interactions and communication
- Review Drug Master Files for compliance
- Manage external consultants and timelines Requirements:
- Eight plus years in pharmaceutical regulatory affairs
- Experienced in Health Canada submission processes
- Successful history managing regulatory teams
- Solid competency in deficiency response
- Familiarity with electronic submission systems Shape the future of pharmaceutical regulations by bringing your strategic expertise to this rewarding role in Mississauga.

📌 Senior Regulatory Affairs Manager – Pharmaceuticals (Mississauga)
🏢 Rossi Recruitment
📍 Mississauga