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p>As member of the Quality System & Compliance group, you will be responsible for the daily operational activities relating to training, documentation and archiving processes:
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p>Pharmaceutical Quality System (PQS): ensure maintenance of the Pharmaceutical Quality System (PQS) at site level:
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Day-to-day operations by maintaining knowledge of company policies, SOPs, and supporting documentsEnsure compliance of local Pharmaceutical Quality System with the company Quality standards by ensuring that all documents are communicated and timely implemented across the siteEnsure robust process for local PQS managementEnsure monitoring at site level, support Quality and Performance metrics Issue related periodic reports when appropriate.
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p>Documentation management
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Coordinate local Community of PracticesEnsure periodic review monitoringAdministrate active BCP once it's activated.Act as key user for the documentation management system (DMS)
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p>Training:
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Provide Training on GMP related topicIssuance of E-LearningSpeachMe administrator
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p>Projects:
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Process improvement of areas under your responsibilitiesImplementation new e-QMS
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p>qualifications
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Bachelor in scientific education2 years in pharmaceutical industryExperience in documentation management and Pharmaceutical Quality System (PQS)Experience in Quality AssuranceFluent in French, basics in English