Descripción
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.
Documentation management
- 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
qualifications
- 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