Senior QMS Admin - Rapid Progression

Responsibilities May Include Some Or All Of The Following:

• Acts in an administrative support capacity for critical QMS processes such as CAPA and audits.
• Review quality records for all related areas of responsibility.
• Responsible for personal daily task management, training plans, and performance management.
• Supports the creation, review, and maintenance QMS documents.
• Provide administrative support for external audits (regulatory or customer).
• Perform User Acceptance Testing (UAT) for electronic Quality Management Systems (eQMS)

Pre-requisites

• Vocational, Associate or bachelor's degree in business administration, scientific discipline, or equivalent experience.
• 1+ years of Quality Management System (QMS) experience working in a regulated Good Manufacturing Process (GMP) environment
• Advanced knowledge of Microsoft Office applications, especially Word and Excel.

Personal competencies

• Capacity to work both independently and in a team-oriented environment;
• Ability to effectively complete the tasks entrusted;
• Capacity to quickly adapt to changing priorities and timelines;
• Strong oral and written communication skills
• Ability to learn quickly and pay attention to detail

Optional competencies

• Practical experience in a regulated industry
• Knowledge of international standards such as ISO 13485
• Knowledge of regulatory requirements relatd to medical devices (Health Canada, FDA, TGA, etc.).
• Other responsibilities as needed.