Process Development Engineer Collaboration drives our success as a market leader in Industrial Precision Solutions and Advanced Technology. Our employees thrive in an environment where we help each other reach our personal best and enable our company to continuously improve and grow, and our customers to succeed. You will find our employees sharing our success by giving back in the communities around the world where we live and work.
We are a global leader in the medical device industry, seeking an experienced and highly motivated individual to join our team in Boyle, Ireland as a Process Development Engineer. We are committed to creating a diverse and inclusive workplace, and we are looking for candidates who share that same commitment.
Summary of the role The Process Development Engineer will manage projects and the identification, specification, introduction, management, and validation of new equipment, processes, products, and technologies, providing technical input and leadership on problem-solving, resolution of technical processing issues, and implementation of process improvements in the area.
Role and Responsibilities Manage, develop and validate new processes 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.).Design and implement new methodologies, materials, machines, processes, or products to bring concepts to market, including essential product and process documentation.Use a science-based approach to develop processes, process improvements, and technology improvements.Understand current processes, taking a hands-on approach to understand 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, troubleshooting, driving effective determination of root cause, and championing a structured approach to problem-solving using lean tools and 6 sigma principles.Complete validation plans, FMEAs, validation protocols, validation reports, control plans, and test method validations supported with appropriate statistical tools in accordance with our 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.1 year minimum 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 and delivering.Energetic and driven self-starter, with good communication and influencing skills.Benefits We offer a flexible work schedule, a comprehensive benefits package, and opportunities for growth and development. Our benefits include: Healthcare cover; Pension contribution; Bike to work policy; Employee Assistance Program; Education Assistance policy; Engagement Company days.
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