Job Description
Job Description
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
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Support Quality Management System activities aligned with ISO and FDA requirements
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Conduct product testing, participate in quality audits, and maintain quality documentation
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Oversee inspection and quality assurance throughout the manufacturing process
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Collaborate cross-functionally to identify process gaps and implement corrective actions
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Analyze quality and performance data and provide actionable insights for improvement
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Lead or support quality systems enhancement projects and ensure timely execution
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Prepare and present quality metrics and reports for leadership review
Qualifications / Skills
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Background in engineering and/or manufacturing processes
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Strong project management skills and ability to prioritize independently
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Strong analytical ability for data interpretation and decision support
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Excellent written and verbal communication skills for cross-functional work
Job Details
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Job Type: Full-time, On-site
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Compensation: $50,000 - $80,000 per year (based on experience)
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Experience Preferred: 1+ year in medical device manufacturing
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Benefits: 401(k), Health Insurance, Dental Insurance, PTO