About this role
Quality Engineer III at Resonetics. Location: Bethel, Connecticut, United States. Role: leading investigations, conducting validations, developing controls Requirements: 2+ years quality engineering experience in medical device manufacturing, familiarity with ISO 13485 and FDA 21 CFR 820, BS in engineering, CQE or Six Sigma certification preferred, Minitab/statistical software experience, technical writing and documentation skills. Category: Quality Assurance Seniority: Entry Level Tools: Statistical software, Minitab, QMS Certifications: cqe, six sigma green belt, six sigma black belt Commitment: Full Time Workplace: Onsite Languages: English