Responsibilities

• Ensure Pharmascience compliance at the Candiac site
• Participate in the management of quality systems such as CC (Change Control), CAPA, DEV (Deviations), 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 address product complaints related to items manufactured at the Candiac site
• Coordinate supplier-related complaints
• Participate in internal audits
• Prepare Quality metrics/indicators
• Support and participate in regulatory and customer audits
• Create and maintain specifications for non-printed materials
• Serve as the client contact for quality systems inquiries
• Participate in various projects aimed at supporting production activities and optimizing procedures