Support Boston Scientific’s Quality Management System through quality data analysis and documentation in a regulated medical device manufacturing setting. 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