About this role
Senior Quality Engineer-Operations-CA at Synchron. Location: San Diego, California, United States. Role: supporting manufacturing, leading validation, driving improvement Requirements: 7+ years quality engineering in FDA-regulated medical device manufacturing, experience with process validation, supplier quality, ISO 13485 and 21 CFR 820, strong statistical and problem-solving skills. Category: Quality Assurance Seniority: Senior Level Tools: SPC, MSA, Gage R&R, GD&T, IQ/OQ/PQ, 5S, Kaizen Certifications: iso 13485 lead auditor, cqe, cqa Commitment: Full Time Workplace: Onsite Languages: English