Elevate your career with GE HealthCare as a Senior Regulatory Manager focusing on CMC strategies. Support pharmaceutical diagnostics projects while overseeing quality sections of product dossiers. This position demands 6+ years of experience combined with a Bachelor's Degree in a related field. You will deliver strategic regulatory input, manage submission documents, and collaborate with global regulatory leads. You'll also guide project teams in data collection while maintaining rigorous document management practices.

Key Responsibilities
• Provide input for CMC regulatory strategies
• Define submission strategies and review regulatory documents
• Guide project planning with global teams
• Maintain registration tracking information
• Support audits and keep updated on regulations

Requirements:
• Bachelor’s Degree with 6+ years’ experience
• Background in diagnostics, pharmaceuticals, or medical devices
• Solid analytical and problem-solving skills
• Knowledge of CMC regulatory requirements
• Experience with electronic document management systems Make a significant impact in the field of regulatory affairs with GE HealthCare's innovative solutions.

📌 Senior Regulatory Manager at GE HealthCare (Quebec City)
🏢 GE Healthcare
📍 Quebec City