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, solid 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
• Strong 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.
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📌 CAPA Specialist at Sanofi Toronto (Ontario)
🏢 Socket.dev
📍 Ontario