**
Medtronic is seeking a Senior Quality Engineer for its validation program, focusing on compliance with FDA, ISO, and cGMP standards while supporting laboratory operations and quality improvement initiatives. The role requires a strong background in validation lifecycle management and quality engineering, emphasizing collaboration across various departments.
**
Job Summary
You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
The Senior Quality Engineer is responsible for managing the site validation program and providing quality engineering support for laboratory operations, special quality improvement projects, and day-to-day quality activities.
Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values.
Matching Summary
Match Score: 75
**
Medtronic is seeking a Senior Quality Engineer for its validation program, focusing on compliance with FDA, ISO, and cGMP standards while supporting laboratory operations and quality improvement initiatives. The role requires a strong background in validation lifecycle management and quality engineering, emphasizing collaboration across various departments.
**
Skills & Requirements
Must-have
Validation lifecycle management
cGMP, FDA, ISO compliance
Risk-based validation strategies
Laboratory quality support
Cross-functional collaboration
Nice-to-have
Process optimization
Validation efficiency initiatives
New product introduction support
Dynamic environment adaptability
Key Requirements
Bachelor's degree in engineering and 4 years of experience
Master's degree with 2 years of experience
PhD with 0 years of experience
Unrestricted U.S. work authorization
Work Rights
Unrestricted U.S. work authorization required for roles below Principal level