Shape creative healthcare solutions as an Associate Regulatory Program Director at Roche in Mississauga. Ensure compliance and quality in global CMC regulatory submissions while driving strategic initiatives.This pivotal role requires a Bachelor’s Degree in life sciences and at least five years of technical regulatory CMC experience. You will develop robust regulatory strategies and interact with Health Authorities globally, emphasizing compliance with c GMP standards and Roche corporate protocols.Key Responsibilities:
- Manage high-quality CMC regulatory submissions globally
- Develop and execute regulatory strategies
- Ensure data accuracy in regulatory documents
- Analyze regulatory risks and opportunities
- Oversee timely responses to Health Authority inquiriesRequirements:
- Bachelor’s Degree in life science disciplines
- Minimum 5 years of industry experience in regulatory CMC
- Proficiency with global Health Authority guidelines
- Technical understanding of drug manufacturing processes
- General awareness of drug development and commercializationInfluence the future of healthcare through regulatory excellence at Roche in Mississauga.#J-18808-Ljbffr

📌 Regulatory Program Director At Roche (Mississauga)
🏢 F. Hoffmann-La Roche
📍 Mississauga