Engineer, Manufacturing - Stryker Limerick (23 month FTC)
Position SummaryProvides Engineering support to a process, project or function. Knows and applies fundamental Engineering and Quality Management System concepts, practices and procedures.
What you will do:Ensure quality of process and product as defined in appropriate OS and Material specifications.Ensure GMPs and system safety.Participate in FMEA, Control Plan, SOP and PPAP generation associated with product transfers and scale ups.Support capital acquisition activity from specifying equipment, contract negotiation, Installation and validation.Provide training for manufacturing team members.Interface with Materials Science, Design and Quality Assurance departments to provide customer with a quality product in a timely manner.Validation, Appraisal and support of coating suppliers, machining suppliers and raw material suppliers e.g. Forgings, titanium etc.Communicate and participate in system and process troubleshooting with support team members and with external agents.Lead and participate cross functional and cross divisional process improvement initiatives.Provide engineering support for new Product and new process introduction, ensuring that all activities are completed and documented in accordance with Stryker New product Development Process.Process validation for products and processes; VP, IQ, OQ, PQ and associated documentation.Conduct Gauge R&R studies for products and new processes.Carry out structured problem solving.Application and development of statistical tools for use in driving continuous improvement projects.What you will need: Level 8 Honours Degree in an Engineering discipline.Has 0- 2 years' experience in a manufacturing environment.Business understanding of operations and there impacts essential.High level of PC Skills required.Strong communication skills with both internal and external stakeholders.Self-starter with demonstrated efficient work methods, analytical & problem solving skills and ability to handle multiple tasks in a fast paced environment.The individual should enjoy working in a dynamic and results motivated team environment.Experience in an FDA regulated or regulated industry beneficial.Ability to effectively work cross-functionally with A.O, Quality, etc.
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