Opportunity Description
Join Roche in Mississauga as a Regulatory Affairs Manager, focusing on enhancing patient care through regulatory compliance in a hybrid role. Your expertise in biologics will be vital.
You will lead the submission processes and collaborate effectively with global Health Authorities in this position. By guiding product lifecycles and optimizing business processes, your role will ensure high-quality team outcomes in regulatory affairs.
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
• S...
You will lead the submission processes and collaborate effectively with global Health Authorities in this position. By guiding product lifecycles and optimizing business processes, your role will ensure high-quality team outcomes in regulatory affairs.
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
• S...
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