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Quick Apply
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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 processes
Strong project management skills and ability to prioritize independently
Strong analytical ability for data interpretation and decision support
Excellent written and verbal communication skills for cross-functional work
Job Details
Job Type : Full-time, On-site
Compensation : $50,000 - $80,000 per year (based on experience)
Experience Preferred : 1+ year in medical device manufacturing
Benefits : 401(k), Health Insurance, Dental Insurance, PTO