Share this job as a link in your status update to LinkedIn.
Category (For Job Seekers): Engineering, Manufacturing/Operations, Quality
Location: EMS FERMOY IRE - Fermoy, CO IE (Primary)
Job Description JOB TITLE: Quality Engineer DEPARTMENT: Quality Department
REPORTING TO: Quality Engineering Lead
About Sanmina Fermoy Our Fermoy, Ireland, facility is FDA registered and certified to ISO ISO13485:2016 for the manufacture of high-quality PCBAs, subassemblies, and complete devices up to and including Class III medical devices.
Sanmina Fermoy's core specialization is manufacturing automation.
We provide services for the entire product lifecycle from New Product Introduction (NPI), prototyping and process validation to complex volume manufacturing & test, shipping and repair.
We create a state-of-the-art environment for manufacturing medical and other high-quality devices.
The facility has a track record of 30 years of outstanding operational performance and customer service, backed by a highly experienced workforce.
We hire people with a range of skills, experience, and backgrounds to fulfill roles in careers such as engineering, quality, and manufacturing to name just a few.
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 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.Quality:Assure ongoing compliance with quality and industry regulatory requirements.Health & Safety:Ensure compliance with Health & Safety Legislation and Regulations.MEASUREMENTS: Yields at Key Process StepsCustomer Return % and Cost (RMA)Scrap %Outgoing Inspection DPM & Customer Incoming Quality LevelsPERSONNEL SPECIFICATIONS ESSENTIAL: Minimum NFQ Level 7 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, PowerPoint, 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 Medical Device Manufacturing Environment or similar.Six Sigma Green or Black Belt CertifiedExperience in New Product Introduction Processes
#J-18808-Ljbffr