Quality Compliance Expert

As member of the Quality System & Compliance group, you will be responsible for the daily operational activities relating to training, documentation and archiving processes:

Pharmaceutical Quality System (PQS): ensure maintenance of the Pharmaceutical Quality System (PQS) at site level:

• Day-to-day operations by maintaining knowledge of company policies, SOPs, and supporting documents
• Ensure compliance of local Pharmaceutical Quality System with the company Quality standards by ensuring that all documents are communicated and timely implemented across the site
• Ensure robust process for local PQS management
• Ensure monitoring at site level, support Quality and Performance metrics
• Issue related periodic reports when appropriate.

• Coordinate local Community of Practices
• Ensure periodic review monitoring
• Administrate active BCP once it's activated.
• Act as key user for the documentation management system (DMS)

Training:

• Provide Training on GMP related topic
• Issuance of E-Learning
• SpeachMe administrator

Projects:

• Process improvement of areas under your responsibilities
• Implementation new e-QMS

• Bachelor in scientific education
• 2 years in pharmaceutical industry
• Experience in documentation management and Pharmaceutical Quality System (PQS)
• Experience in Quality Assurance
• Fluent in French, basics in English