Graduate Process Development Engineer

A Graduate Process Development Engineer is required by CareerWise Recruitment for our client based in Roscommon. The Graduate Process Development Engineer will support 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. It is essential that Graduates have at LEAST 1 year’s Manufacturing experience, preferably in a Medical Devices company.

THE ROLE:

• Support, 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 the 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

REQUIREMENTS:

• Degree (Level 8) 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 do further include: o Healthcare cover; o Pension contribution; o Bike to work policy; o Employee Assistance Program; o Education Assistance policy; o Engagement Company days

Please call Tom Devaney today for further information on 091-758771 or email: tdevaney@careerwise.ie

CareerWise Recruitment (In Search of Excellence) Established in 1999, CareerWise Recruitment specialises in recruitment of management and technical professionals for the life sciences, ICT, engineering, food and agri sectors.

We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway, Mayo and Dublin.

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