Spécialiste en conformité et systèmes qualité gérant les systèmes qualité pour Pharmascience. Gestion des audits, déviations, et spécifications sur le site de Candiac.
Responsibilities
Participate in the management of quality systems such as Change Control (CC), Corrective and Preventive Actions (CAPA), Deviations (DEV), Audits, and Risk Management
Coordinate and prepare annual product reviews
Review and approve change control actions and minor changes
Investigate and address deviations related to the Quality/Compliance department
Investigate and manage complaints related to products manufactured at the Candiac site
Coordinate supplier complaints
Participate in internal audits
Prepare Quality indicators/metrics
Participate in/support regulatory and customer audits
Create and maintain specifications for non-printed materials
Serve as the client contact for questions related to quality systems
Participate in various projects aimed at supporting production activities and optimizing procedures
Requirements
Three (3) to five (5) years of experience in a similar role within the pharmaceutical industry
Knowledge of Good Manufacturing Practices (GMP) for Canada, the United States, and Europe
Excellent verbal and written communication skills with internal and external stakeholders
Strong knowledge of risk management tools
Excellent planning and organizational skills
Strong problem identification and resolution skills
Rigour and attention to detail
Proficiency with the Microsoft Office suite
TrackWise and SAP (an asset)
Bilingual in French and English, both spoken and written: The incumbent will need to collaborate with suppliers and/or customers located outside the province of Quebec.
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