Job Description
Drive Roche's patient care mission as an Associate Regulatory Program Director in Mississauga, Ontario. This hybrid role focuses on shaping global regulatory strategies and managing CMC submissions.
Roche is seeking a leader with over 5 years of pharmaceutical regulatory experience. You will play a crucial role in preparing regulatory submissions, collaborating with global partners, and engaging health authorities to ensure compliance. This position demands leadership in managing regulatory relationships and addressing international regulator inquiries efficiently.
Key Responsibilities: • Prepare high-quality CMC regulatory submissions for health authorities • Conduct strategic meetings with global regulatory partners • Collaborate on lifecycle management of synthetic and biologic products • Support compliance through thorough team deliverables • Address inquiries from international regulators in a timely manner
Requirements: • Bachelor’s degree in life scien...
Roche is seeking a leader with over 5 years of pharmaceutical regulatory experience. You will play a crucial role in preparing regulatory submissions, collaborating with global partners, and engaging health authorities to ensure compliance. This position demands leadership in managing regulatory relationships and addressing international regulator inquiries efficiently.
Key Responsibilities: • Prepare high-quality CMC regulatory submissions for health authorities • Conduct strategic meetings with global regulatory partners • Collaborate on lifecycle management of synthetic and biologic products • Support compliance through thorough team deliverables • Address inquiries from international regulators in a timely manner
Requirements: • Bachelor’s degree in life scien...