Job Description
Drive impactful regulatory strategies at Roche in Mississauga as a Pharmaceutical Regulatory Program Manager. Enhance compliance and innovation while making a difference in patient care.
In this hybrid role, you will work with a cooperative team to lead regulatory submissions and interact with global Health Authorities. Your experience will be key in navigating the complexities of biologics and ensuring high standards throughout the product lifecycle.
Key Responsibilities
- Oversee submission of CMC regulatory documents
- Facilitate strategic meetings with Health Authorities
- Guide product lifecycles with cross‑functional partners
- Ensure high‑quality completion of team deliverables
- Optimize business processes for regulatory excellence
Requirements
- Bachelor’s in life sciences; postgraduate is advantageous
- Minimum 3 years in regulatory affairs or quality
- Expertise in drug develo...