Engineer - IQA

Description

Sanmina Corporation (Nasdaq: SANM) is a global powerhouse in integrated manufacturing solutions serving the fastest growing segments of the global Electronics Manufacturing Services (EMS) market. We are a global engine providing the end-to-end manufacturing backbone for the world's most essential and innovative brands. Whether it's autonomous vehicles, life-saving medical tech, next-gen aerospace, or AI/cloud infrastructure - our integrated solutions don’t just meet standards—they redefine them. Business Title : Engineer – IPQA Role: The Role of the Engineer in Quality department is to handle the Product & Process Quality performances Work towards delivering Customer requirements and Expectations. Monitor the Performance of the Product / Process, Conduct Internal Quality meeting and drive for Continuous Improvements. Focus on Departmental KPI and achieve the Target. Academic Qualification / Job Qualification: Diploma in EEE or ECE or E & I or Mech with more than 8 ~10 years experience (or) BE in EEE or ECE or E&I or Mech with 6~ 8 years experience Skills / competence required to perform the Job: 1. Team player 2. Good knowledge in MS Office. 3. Good communication & interpersonal skills 4. Experience in EMS or OEM industry preferably Electronics Manufacturing industry 5. QMS Knowledge of ISO 13485/AS9100 / ISO 9001/TS16949 6. Knowledge in Statistical Process control, Measurement System analysis & CAPA. 7. Knowledge on IPC 610 Standards. Responsibilities: 1. CAPA implementation and effectiveness monitoring. 2. Periodically review and update Quality Procedures 3. Manufacturing Process audit & Compliance 4. Data collection, Trending, analysis and drive improvements 5. Review and Monitor Validation Builds as per applicable standards 6. Statistical tools (7QC, WHY-WHY analysis, Fault tree / factor analysis, Risk assessment). 7. FAR & DHR (Device History Record) review and approve. 8. Closely Coordinate & Monitor the NCMR & RMA process 9. Active participation in EHS related activities. Authority: 1. Authorized to review and approve the new line qualification and Process validation documents. 2. Authorized to approve Engineering change note with respect to verification and line implementation. 3. Authorized to take quick and correct decisions with respect to the effectiveness CAPA implementation and updating the system procedures. 4. Authorized for Line stop and shipment hold in case of quality deviation and which impacts the Customer.