JWR Employment Specialists are recruiting a Process Development Engineer for a Medical Device manufacturing company located in Boyle.
The Process Development Engineer will be responsible for managing projects and the identification, specification, introduction, management and validation of new equipment, processes, products and technologies. They will provide technical input and leadership on problem solving, resolution of technical processing issues and implement process improvements.
The role will offer an attractive salary and benefits.
Duties include; Manage, develop and validate new process including running trials/feasibility studies for new product /product iterations and new technology to demonstrate capability and achieve key project deliverables (Cpk, cycle times, lead-time, GM% etc.) Designs and implements new methodologies, materials, machines, processes or products to bring concept to market, including essential product and process documentation Uses a science-based approach to develop processes, process improvements and technology improvements Understand current processes, taking a hands-on approach to understanding how these can be applied to new opportunities Work with equipment and material vendors to mutually understand their and our technical process challenges, to improve capability and eliminate cost Prepare project plans that specify project phases, tasks, task interdependencies, durations, resource assignments, and costs Write and review new customer development proposals for development projects Identify, develop and implement plans for continuous improvement activities Lead improvement initiatives as assigned including investigations, trouble shooting, driving effective determination of root cause and championing a structured approach to problem solving using lean tools and 6 sigma principals Complete validation plans, FMEAs, validation protocols, validation reports, control plans and test method validations supported with appropriate statistical tools in accordance with quality system and the requirements of ISO13485, The Medical Device Regulation and FDA Quality System Regulations Assess customer's validation needs and propose innovative solutions Support teams to identify and specify new technology/tooling/materials required Skills and Qualifications: Degree in a relevant engineering, science or an equivalent discipline 3+ year's work experience in industry, Medical device or manufacturing experience is essential A Practical level-headed individual with strong technical ability Ability to work hands-on, with a solid engineering background, engaging cross-functional groups, equipment and material vendors to resolve technical issues Project management skills, setting realistic objectives Energetic and driven self-starter, with good communication and influencing skills
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