Found Description
Elevate healthcare delivery as a Regulatory Program Manager with Roche in Mississauga. This hybrid role focuses on driving regulatory strategy and ensuring compliance in biologics.
As a key leader at Roche, you will manage CMC regulatory submissions while collaborating with global Health Authorities. Your expertise will guide product lifecycles, optimize business processes, and ensure quality team deliverables to enhance patient care.
Key Responsibilities:
• Oversee submission of CMC regulatory documents
• Facilitate strategic meetings with Health Authorities
• Guide product lifecycles with cross-functional teams
• Ensure high-quality completion of team deliverables
• Optimize business processes for regulatory excellence
Requirements:
• Bachelor's in life sciences; postgraduate is a plus
• Minimum 3 years in regulatory affairs or quality
• Expertise in drug development and quality attributes
• Strong decision-making and communication skills
• Coop...
As a key leader at Roche, you will manage CMC regulatory submissions while collaborating with global Health Authorities. Your expertise will guide product lifecycles, optimize business processes, and ensure quality team deliverables to enhance patient care.
Key Responsibilities:
• Oversee submission of CMC regulatory documents
• Facilitate strategic meetings with Health Authorities
• Guide product lifecycles with cross-functional teams
• Ensure high-quality completion of team deliverables
• Optimize business processes for regulatory excellence
Requirements:
• Bachelor's in life sciences; postgraduate is a plus
• Minimum 3 years in regulatory affairs or quality
• Expertise in drug development and quality attributes
• Strong decision-making and communication skills
• Coop...