As a 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 and 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 topics.
* Issuance of E-Learning.
* SpeachMe administrator.
Projects
* Process improvement of areas under your responsibilities.
* Implementation of 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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