Cyient
Key Responsibilities Support supplier qualification and onboarding activities Assist in supplier audits (process/product quality) Monitor supplier performance and quality metrics Drive root cause analysis (RCA) and CAPA closure Review incoming quality issues and supplier deviations Ensure compliance with regulatory standards (QMS) Support PPAP / APQP / FAI documentation (as applicable) Collaborate with cross-functional teams (R&D, manufacturing) Required Skills Basic understanding of quality tools (7 QC tools, RCA) Familiarity with ISO 13485 / FDA 21 CFR (preferred) Knowledge of engineering drawings & specifications Strong analytical and problem-solving skills Good communication and stakeholder coordination Educational Qualification BE / BTech – Mechanical / Electronics / Electrical (or equivalent) Experience 4 - 8 years Preferred Exposure to medical device industry Awareness of risk management (ISO 14971 basics)