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 • Robust 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. #J-18808-Ljbffr