Enhance production efficiency as a Technical Administrator at Sanofi in Toronto. Your expertise in microbiology and GMP compliance will directly contribute to cutting-edge vaccine solutions.

In this fixed-term contract role spanning three years, you will administer downstream production activities, ensuring accuracy in documentation and regulatory compliance with cGMP and HSE standards. Your responsibilities include training staff, coordinating production activities, and maintaining the integrity of operations through strict adherence to quality practices.

Key Responsibilities:
• Oversee downstream production documentation compliance
• Coordinate safety inspections and hazard reporting
• Operate centrifuges and chromatography for antigen purification




• Enter and track data in SAP and Pharm Net Web
• Support process improvement projects and documentation

Requirements:
• Bachelor's degree in Biochemistry, Microbiology, or Bioengineering
• Minimum four years’ related work experience
• Strong knowledge of microbiology and aseptic techniques
• Proficiency in SAP and technical writing
• Familiarity with data analysis tools and problem-solving

Bring your technical expertise and passion for life sciences to support Sanofi’s mission in Toronto.
#J-18808-Ljbffr

📌 Technical Administrator in Biopharma (Ontario)
🏢 Sanofi
📍 Ontario