Quality Engineer III provides Quality Engineering support for Operations to ensure compliance with Quality System requirements for medical device manufacturing/operations.
Requirements
- Bachelor’s Degree in Engineering or related field or 5+ years of experience in a quality engineering role within a regulated industry.
- 5+ years' experience at Quality Engineer level II in medical device or regulated manufacturing.
- Knowledge of Quality Engineering Tools and Techniques, FDA regulations, ISO 13485:2016, and other relevant regulations and industry standards.
- Proficient in Microsoft Office and Minitab, ability to multitask, and strong communication skills.
Benefits
- Medical, dental, and vision benefits-effective on date of hire
- Generous paid time off benefits and 10 paid Holidays
- 136 Hours PTO (prorated based on hire date)
- Company-paid life insurance
- 401k plan with company match
- Well-Being benefits (low-cost nutrition and mental health visits, discounted gym membership, pet insurance, etc.)
- Career Growth benefits (tuition reimbursement, on-site training programs, defined career path, etc.)