Quality Engineer II
Medtronic · Mystic, CT
QualityFull-time$79k–$119kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Quality Engineer II supports quality system activities in a regulated medical device manufacturing environment at Medtronic's Mystic, Connecticut facility. The role focuses on nonconformance management, CAPA activities, calibration compliance, and process validation while collaborating with cross-functional teams to maintain regulatory compliance and drive continuous improvement.
What they're looking for
- Bachelor's degree with minimum 2 years relevant experience, or Master's degree
- Experience with quality system processes in regulated manufacturing
- Experience conducting nonconformance investigations and root cause analysis
- Working knowledge of quality documentation and regulatory compliance standards
- Ability to manage multiple projects while maintaining accurate documentation
- Medical device industry experience (preferred)
- Familiarity with TrackWise quality management systems (preferred)
What you'll be doing
- Support nonconformance investigations and implement corrective actions with cross-functional teams
- Facilitate CAPA activities including documentation, verification, and closure
- Maintain calibration program compliance and support calibration quality activities
- Execute process and equipment validation activities including IQ, OQ, and PQ
- Analyze quality data and trends to identify improvement opportunities
Privacy & handoff
This role links to Medtronic's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.