Job Description
Drive quality assurance as a Compliance Specialist in the Medical Devices sector. Ensure conformity with ISO 9001 and Canadian Medical Device Regulations, whilst supporting QA initiatives.
You will contribute to regulatory compliance by managing documentation and execution of Field Actions related to devices. The role includes aiding in audits and refining quality processes to align with corporate requirements, maintaining a responsive approach to internal and customer queries. This position also emphasizes regular review and update of QMS adherence.
Key Responsibilities
- Monitor compliance with Canadian Medical Device Regulations
- Support timely implementation of Field Actions
- Participate in the management of Quality Management Systems
- Assist manufacturers with audits for MDSAP
- Respond to Quality-related commercial requests
Requirements
- Bachelor’s degree in Science, Biology, or Quality
- Minimum 2 years experience in Medical Devices
- Knowledge of ISO 9001 quality systems
- Strong skills in Microsoft Office Suite
- Excellent collaboration and time management skills
Leverage your quality assurance expertise to enhance compliance and support organizational goals effectively.
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