Join Sanofi's team in Toronto as a Deviation and CAPA Specialist. Play a crucial role in enhancing compliance and training across manufacturing and supply chains.

In this 18-month fixed-term role, you will assist in the management of the Deviation and CAPA quality systems, ensuring processes meet regulatory standards. Candidates should have solid experience in quality management, along with outstanding organizational and communication skills. This role also involves supporting training initiatives and continuous improvement processes.

Key Responsibilities: • Assist in the ownership of Deviation and CAPA processes • Carry out regular data validations for compliance • Facilitate the development of quality-related training • Assess risks and support mitigation strategies • Collaborate on continuous process improvements

Requirements: • Bachelor's degree in relevant discipline • 2–5 years experience in pharmaceutical quality systems • Proficient in document review and management • Solid analytical skills for trend identification • Excellent verbal and written communication skills

Bring your quality management experience to enhance operations at Sanofi in Toronto. #J-18808-Ljbffr

📌 Quality Management Role in Toronto (Winnipeg)
🏢 Socket.dev
📍 Winnipeg