At a Glance
- Tasks: Lead CMC submissions and drive regulatory strategies for global health authorities.
- Company: Join Roche, a leader in the pharma industry, located in Mississauga.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with diverse stakeholders.
- Why this job: Make a significant impact on product lifecycle and regulatory compliance.
- Qualifications: Experience in biologics or related fields is preferred.
The predicted salary is between 103500 - 126500 $ per year.
Roche in Mississauga seeks an Associate Regulatory Program Director in Pharma Technical Regulatory to lead CMC submissions to global health authorities and drive regulatory strategies across the product lifecycle.
You will partner with multiple stakeholders to ensure data integrity in regulatory information management systems and deliver timely, compliant regulatory documents.
A background in biologics or related areas is a plus; relocation is not offered.
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Associate Regulatory Program Director in Mississauga employer: Roche
At Roche, we pride ourselves on being an exceptional employer that values diversity and fosters a culture of open dialogue and collaboration. Located in Mississauga, our team is dedicated to driving innovation in healthcare while providing ample opportunities for personal and professional growth. With a commitment to inclusivity and continuous improvement, Roche empowers employees to thrive and make a meaningful impact in the lives of patients worldwide.
