QC Co-Ordinator

at  Sanofi US

EXPERIENCE:

• Minimum 2 years of operational experience of quality laboratories in a fast-moving manufacturing environment

SOFT SKILLS:

• Well organised, methodical in approach
• Excellent accuracy and attention to detail
• Demonstrated ability to embrace change and innovation and to initiate new and improved ways of working
• Excellent communication skills and ability to work effectively in cross-functional teams and can take ownership
• Willingness to learn new techniques
• Strong on electronic systems

TECHNICAL SKILLS:

• Knowledge of quality management systems
• Understand relevant quality/compliance regulations
• Good working knowledge of Laboratory GxP processes

EDUCATION:

• Science Degree/Project management or equivalent

IF THIS DESCRIPTION RESONATES WITH YOUR SKILLS / EXPERIENCE AND SPARKS YOUR INTEREST, WE ENCOURAGE YOU TO TAKE THE NEXT STEP AND APPLY. WE LOOK FORWARD TO CONNECTING WITH YOU SOON!

Discover our Code of Conduct, that serves as the moral compass that guides us when chasing the miracles of science to improve people’s lives. Please ensure to have read this document, before applying.
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Pursue Progress, Discover Extraordinary

• Define, manage and maintain a documentation control system for QC cGMP Documents
• Support schedule all stability and release testing for the relevant QC team
• Ensure all instrument calibrations/qualifications are taken into consideration when scheduling
• Prepare long term and short-term capacity plans for the relevant labs
• Analyse long term forecasts to identify possible capacity and material issues
• Develop annual capacity plans
• Recognise and implement continuous improvement activities to increase flexibility, eliminate waste, reduce cycle time and cost while maintaining product supply to internal and external customers
• Create and update procedures when required
• Generate required documentation to support health authority requests
• Manage documentation issuance for the lab test teams; manage external documentation requests
• Ensure continued laboratory capability