Quality Engineer

CPL

Galway

A manufacturing company is currently looking for a Quality Engineer to join their team in Galway city. Reporting: Senior Quality Engineer. Overview: Quality Engineer is responsible for leading quality engineering activities for manufacturing processes, materials, and products. Other activities may be assigned as needed. Responsibilities : Lead Quality Engineering support at the companies manufacturing process driving process continuous improvements and providing manufacturing support, this includes: Process/manufacturing data analysis, trending, and assisting yield reporting. Investigation root cause analysis of quality issues in manufacturing and managing quality related NC’s and CAPA’s. Establish analysis techniques and other quality control tools such as SPC, Cpk, Ppk. Lead the Materials Review Board (MRB) process. Address ongoing compliance. Champion continuous process improvement and, in conjunction with other functions, analyse feedback and identify and implement appropriate problem solving and statistical techniques to improve quality of manufactured product and overall effectiveness and efficiency of processes. Establish inspection plans, frequencies and test methods for incoming material/parts. Overall responsibility for GMP standards and compliance within the companies manufacturing area. Drive risk management activities in manufacturing (Process FMECA. Manage process quality control system to ensure all manufactured product meets defined specifications prior to shipment. Manage assigned aspects of the quality system in compliance with ISO 13485:2003, 2012. FDA QSR, MHLW and Canadian Quality System requirements. Conduct internal audits as defined by audit schedules. Quality system training of company personnel as per defined training plans. Perform other assigned tasks and support all aspects of the Quality System as directed by the Manager. Requirements: Ability to work on own initiative. Strong team member with the ability to identify and drive implementation of innovative quality improvements. Ability to consistently meet deadlines. Demonstrate and actively promote high levels of professional quality engineering. Good communication skills. Must have the ability to communicate effectively at all levels of the company. Ability to write clear, concise technical protocols and reports. Good administrative/organizational ability with high level of attention to detail. Ability to liaise with suppliers, customers and regulatory contacts in an informed professional manner. Thorough understanding of ISO 13485:2003, 2012 and FDA QSR. Education / Experience BE/BS Degree. A Post-graduate qualification in Quality Assurance is preferable although not mandatory. At least three to five years Quality Engineering experience or related role within the medical device industry. Interested candidates please contact Rebecca Meaney on +35391507509 or email your CV to rebecca.meaney@cpl.ie. This job originally appeared on RecruitIreland.com.

2598 days ago