Quality Assurance Engineer (QMS Specialist)

You will also have the opportunity to work with other like-minded, self-directed and detail-oriented Top Talents in an extremely collaborative and professional environment.

Primarily responsible for facilitating document and product related changes in accordance with our clients change management procedures and relevant regulatory requirements for medical devices.

Fluent in English and French

Key Responsibilities:

Facilitate the change management process for document and product related changes.Perform administrative activities related to Stryker's learning management system.Assist with the migration of QMS related documentation from local document management systems to PLM system (Windchill).Ensure QMS documentation reflects actual business activities while remaining compliant with applicable internal and external regulatory requirements including but not limited to Site, Division, Corporate, FDA, ISO, MDD, MDR and individual country requirements.Drive Good Manufacturing Practices and Good Documentation Practices.Identify and implement improvement opportunities to increase the efficiency and effectiveness of the QMS and associated documentation.Develop and deliver training for QMS areas of expertise.Engage with IT team in relevant PLM system discussions.