
Manager Regulatory Affairs
20 hours ago
**Manager Regulatory Affairs**
Select your preferred frequency for receiving alerts:
Contract Type: Full-time Employment / Unlimited
Job Reference ID: 8812
Manager Regulatory AffairsElevate Your Professional Growth
Key Responsibilities:
Regulatory Operations
- Build and maintain relationships with DRAP offices and branches.
- Ensure compliance with regulatory standards for company products.
- Work closely with management to inform decision-making on regulatory matters.
- Develop and submit product registration dossiers to DRAP.
- Expertise in DRAP regulatory submission software.
- Oversee timely submission of variations to registration applications and renewals.
- Provide strategic guidance on regulatory matters and resolve complex issues.
- Coordinate license application submissions to regulatory bodies.
- Facilitate collaboration between Provincial Quality Control Boards.
Industry Insights
- Establish relationships with key stakeholders at federal and provincial levels.
- Stay current on industry developments, including new registrations, approvals, and price fixations.
- Monitor market trends and competitor activity.
- Gain valuable insights into Ministry of Health proceedings.
- Negotiate with regulatory bodies on pricing and reviews.
We strive to advance medical knowledge and improve patient outcomes.
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