Responsable de la conformité et des systèmes qualité au sein de Pharmascience sur le site de Candiac. Participation à la gestion des audits internes et des systèmes qualité pour assurer la conformité.
Responsibilities
Ensure Pharmascience's compliance at the Candiac site.
Participate in the management of quality systems such as Change Control (CC), CAPA, deviations (DEV), audits, and risk management.
Coordinate and draft annual product reviews.
Review and approve change control actions and minor changes.
Investigate and address deviations related to the Quality/Compliance department.
Investigate and handle complaints related to products manufactured at the Candiac site facilities.
Coordinate supplier complaints.
Participate in internal audits.
Prepare Quality indicators.
Participate in/support regulatory and customer audits.
Create and maintain specifications for non-printed materials.
Serve as the client liaison for questions regarding 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 Canadian, US and European Good Manufacturing Practices (GMP).
Proficiency with Microsoft Office suite.
TrackWise and SAP (an asset).
Benefits
Hybrid work arrangement.
Excellent verbal and written communication skills.
Good knowledge of risk management tools.
Excellent planning and organizational skills.
Bilingual in French and English, both spoken and written.
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