Sanmina Corporation (Nasdaq: SANM) is a leading integrated manufacturing solutions provider serving the fastest-growing segments of the global Electronics Manufacturing Services (EMS) market.
Recognized as a technology leader, Sanmina Corporationprovides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors.
Sanmina Corporation has facilities strategically located in key regions throughout the world.
OBJECTIVES OF POSITION:
•Primary objective is to ensure customer satisfaction by monitoring, controlling and improving all related customer processes.
•Principal customer interface for Quality metrics and improvement initiatives. Identifies, plans, and organizes regulatory affairs for ensuring compliance with the FDA’s Quality System Regulations, ISO 9000, ISO 13485:2003, JPAL as well as all international standards relevant to customer products for Sanmina-SCI manufacturing facility.
RESPONSIBILITIES:
•Management of closed loop customer complaints and improvement processes.
•Generation and Review and review of Quality Metrics System.
•Overall responsibility for DMR/DHR and Technical Files.
•Data collection, analyzing and reporting.
•Pareto and trend analysis.
•Initiate and drive Continuous Improvement programs.
•NPI Approval including First Article Inspections and Reporting.
•CAPA, NCM and RMA analysis and Improvement.
•QSR Validation protocols and report (IQ, OQ & PQ).
•Conducting Audits to ensure conformance and effectiveness of the Quality System.
MEASUREMENTS:
•Yields at Key Process Steps
•Customer Satisfaction Index, (CCN, CSO etc)
•Customer Return % and Cost (RMA)
•Scrap %
•Outgoing Inspection DPM & Customer Incoming Quality Levels
PERSONNEL SPECIFICATIONS
ESSENTIAL:
•Degree / Diploma in Science or Engineering, or a lesser qualification with sufficient job related experience
•At least 2-3 years Quality Assurance / Regulatory affairs experience. In a similar Quality Engineering role in the electronics manufacturing industry.
•Sound understanding and utilization of Problem Solving Techniques
•Proficient in the use of Microsoft Word, Power-point and Excel.
•Good Communications and influencing skills.
•Ability to respond to common inquiries or complaints from internal customers and regulatory agencies. Ability to write standard operating procedures, training documents, and regulatory responses.
DESIRABLE:
•Experience in working within a Class 3 Medical Device Manufacturing Environment.
•Six sigma Green or Black Belt Certified
•Experience in New Product Introduction Processes
Please apply with your CV and cover letter by the 'apply' button below.
Please use "Qreer.com" as reference in your application.
Education Backgrounds: |
Electrical Engineering Healthcare Science |
Specialties: |
Manufacturing Quality Engineering |
Education Level: |
Undergraduate (Bachelors) Postgraduate (Masters) |
Experience: |
10 - 15 years 2 - 5 years 5 - 10 Years |
Languages spoken: |
English |
Job Location: | Fermoy, Ireland |
Type: Job
Deadline: 11th August 2013
Job reference (ID): 5866
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