The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing
Job Summary
The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing.
Employees are immediately eligible to participate in a comprehensive benefits package including medical, dental, vision, disability, life insurance, and a 401(k) plan with company matching contributions.
The role requires monitoring manufacturing processes, reviewing Bill of Materials changes, and leading complaint investigations while ensuring compliance with FDA regulations.
Matching Summary
The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing.
Salary
Base: $77,570 - $113,740; Bonus/Equity: Cash-based incentive program available; Benefits: Comprehensive package with immediate eligibility including medical, dental, vision, 401(k) match
Skills & Requirements
Must-have
Bachelor's Degree in Engineering
2-5 years quality engineering experience
FDA regulations and QMS knowledge
Device History Records maintenance
Statistical quality control tools
Nice-to-have
Ability to work independently and in team environment
Experience with supplier quality resolution
Mentoring quality inspectors and technicians
Continuous improvement project participation
Key Requirements
Minimum Bachelor's Degree in Engineering or related field
2-5 years quality engineering experience
Preferably in medical device or regulated manufacturing