Quality Engineer

We are seeking a detail-oriented Quality Engineer to support quality systems, manufacturing quality, and continuous improvement activities within a regulated medical device environment. Key Responsibilities Support NCR, CAPA, deviation, and quality investigation activities Assist with root cause analysis and corrective action implementation Review manufacturing and quality documentation Support internal audits and regulatory inspection readiness Participate in process improvement and defect-reduction initiatives Collaborate with Manufacturing, Supplier Quality, and Engineering teams Maintain compliance with applicable quality requirements Required Qualifications Bachelor\'s degree in Engineering, Life Sciences, or related field 0–3 years of Quality Engineering or regulated manufacturing experience Basic understanding of CAPA, NCR, and Quality Management Systems Strong analytical and technical documentation skills Preferred Skills Knowledge of ISO 13485 and FDA quality requirements Familiarity with root cause analysis tools Medical device manufacturing experience is preferred #J-18808-Ljbffr