Job details
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
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Nils Bellieres
- Randstad Merck Aubonne