Support Boston Scientific’s Quality Management System through quality data analysis and documentation in a regulated medical device manufacturing environment. This six-month contract suits early-career professionals.

The Quality Systems Analyst I supports compliance, effectiveness, and continuous improvement activities. You will maintain quality records, monitor metrics, and assist with procedures, audits, training, and document control. The role provides exposure to CAPA, nonconformance management, change control, management review, supplier quality, and root cause analysis.

Key Responsibilities:

- Administer and maintain the Quality Management System
- Collect, organize, and analyze quality data and metrics
- Prepare, review, and revise quality documents and records
- Support audits, training,



document control, and management review
- Participate in investigations, improvement activities, and root cause analysis

Requirements:

- Bachelor’s degree in science, engineering, quality, or related field
- Zero to one year of relevant experience
- Solid attention to detail and documentation skills
- Effective written, verbal, and organizational skills
- Microsoft Office proficiency and willingness to learn

Build Quality Systems experience at Boston Scientific while supporting compliance, patient safety, product quality, and continuous improvement.

📌 Quality Systems Analyst Medical Devices (Ottawa)
🏢 Boston Scientific
📍 Ottawa