We are looking for a Quality Engineer who will help maintain and strengthen quality systems within a regulated manufacturing environment. The ideal candidate will support compliance efforts, improve quality processes, and drive continuous improvement initiatives.
Key Responsibilities
- Support Quality Management System activities aligned with ISO and FDA requirements
- Conduct product testing, participate in quality audits, and maintain quality documentation
- Oversee inspection and quality assurance throughout the manufacturing process
- Collaborate cross-functionally to identify process gaps and implement corrective actions
- Analyze quality and performance data and provide actionable insights for improvement
- Lead or support quality systems enhancement projects and ensure timely execution
- Prepare and present quality metrics and reports for leadership review
Qualifications / Skills
Background in engineering and / or manufacturing processesStrong project management skills and ability to prioritize independentlyStrong analytical ability for data interpretation and decision supportExcellent written and verbal communication skills for cross-functional workJob Details
Job Type : Full-time, On-siteCompensation : $50,000 - $80,000 per year (based on experience)Experience Preferred : 1+ year in medical device manufacturingBenefits : 401(k), Health Insurance, Dental Insurance, PTO