At a Glance
- Tasks: Lead Health Authority interactions and craft regulatory strategies for drug filings.
- Company: Join Roche, a global leader in healthcare innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on cross-functional excellence.
- Why this job: Make a real impact on global health by ensuring timely regulatory approvals.
- Qualifications: Experience in regulatory affairs and strong communication skills.
The predicted salary is between 135000 - 165000 $ per year.
Roche Holding AG in Mississauga seeks an Associate Regulatory Program Director in Pharma Technical Regulatory (PTR) to lead Health Authority interactions for CMC information across IND/IMPD/NDA filings. You’ll partner with stakeholders across the product lifecycle and support cross-functional regulatory excellence.
In this role you will:
- Craft regulatory strategies
- Ensure data integrity in regulatory documents
- Drive timely regulatory approvals while navigating global guidelines
Global Regulatory Lead CMC & Health Authority Strategy in Mississauga employer: Roche Holding AG
At Roche, we pride ourselves on being an exceptional employer that champions innovation and professional growth. As a Pharmaceutical Learning Business Partner Lead, you will thrive in a collaborative work culture that values your expertise and encourages the development of cutting-edge learning strategies. With access to global resources and a commitment to transforming healthcare education, Roche offers unparalleled opportunities for meaningful impact and career advancement in a dynamic environment.
