About this role
Quality Manufacturing Engineer at Molded Devices (Aptyx). Location: Charlotte, North Carolina, United States. Role: supporting manufacturing, leading investigations, conducting audits Requirements: Bachelor's in Engineering, 3–5 years quality engineering in medical device manufacturing, CAPA and root cause analysis experience, knowledge of FDA 21 CFR Part 820 and ISO 13485, validation (IQ/OQ/PQ) and statistical methods; Six Sigma Green Belt and CQE preferred. Category: Engineering Seniority: Mid Level Tools: Microsoft Office Certifications: six sigma green belt, asq cqe Commitment: Full Time Workplace: Onsite Languages: English