Elevate quality processes as a Deviation and CAPA Specialist at Sanofi’s Toronto facility. Contribute to compliance and training initiatives while ensuring high-quality standards in manufacturing operations. This fixed-term position for 18 months requires supporting the Business System Owner Manager with the Deviation and CAPA quality systems.

Key skills include expertise in quality management systems, robust analytical abilities, and excellent communication. This role plays a pivotal part in maintaining site compliance and aligns training programs with global standards. Key Responsibilities:
Support ownership of quality Deviation and CAPA processes
Conduct routine data quality checks and validations
Develop and deliver training programs for quality systems




Identify process risks and implement mitigation strategies
Support continuous improvement initiatives in manufacturing Requirements:
Bachelor's degree in a relevant field
2–5 years experience in pharmaceutical quality management
Robust document management and analytical skills
Excellent communication abilities for cross-department collaboration
Ability to navigate compliance with regulatory standards Utilize your expertise in CAPA and Deviation management to enhance quality assurance at Sanofi in Toronto.

📌 Capa Specialist At Sanofi Toronto (Canada)
🏢 Socket.dev
📍 Canada