Tech III - Athlone

Start free →

Or apply yourself on the official page →

About the role

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life At our Advanced Manufacturing Engineering Department in Medtronic Athlone, we focus on NPI (new product introduction) and Product Transfers of Medical Devices into our Controlled Manufacturing Environment. Manufacturing & Quality Engineers, Project Managers & Technicians are directly involved new product introductions, product transfers and validating/continuously improving product lines by ensuring time-efficient and cost-effective processes while maintaining overall product quality and compliance. Responsibilities may include the following and other duties may be assigned.   • Working with the Advanced Manufacturing Engineering and supporting Operations teams to contribute to the development and qualification of robust processes for new products. • Aids in design of packaging and labelling processes, procedures and packaging layouts for assemblies, equipment installation, processing, machining and material handling and fabrication of tools. • Designs arrangement of packaging and labelling machines within plant facilities to ensure most efficient and productive layouts. • Designs sequence of operations and specifies procedures for the fabrication of packaging tools and equipment and other functions that affect product performance. • Inspects performance of machinery, equipment, and tools to verify their efficiency. Support technical root cause investigations and implement corrective actions. • Ensures processes and procedures are in compliance with regulations. Contributes to New Product Introduction (NPI) function to define, execute and deliver on NPI requirements. • Leads verification, validation, and implementation of package systems for both design and process development. • Develops technical documentation including design specs, input requirements, validations and technical reports in accordance with quality system requirements. • Utilises project management skills to gain alignment, lead cross functional teams, and drive continuous improvement projects that focus on “best in class” outcomes.   Key Skills & Experience • Level 6 or higher qualification in Engineering or Science related discipline , with 2 years of relevant experience • Experienced in working with DFA (Design for Automation), Lean Sigma, Analytical packages incl. Minitab advantageous. • Experience working with manufacturing documentation (MP, IP, BOM, CDP, IQ, OQ, PQ). • Strong verbal and written communication skills. • Computer literate; word processing, spreadsheets, Solid works, AutoCad. • Knowledge of materials associated with medical devices such as polymers (nylons, PVC, polyethylene, polypropylene, Pebax, PTFE, polycarbonate, films, Tyvek, etc.). • A dynamic team player who can work effectively and proactively on cross-functional teams. An effective and creative problem solver • Can work independently with general supervision. • Energetic, self-driven with a tenacious drive for results and motivated to ensure on-time, high-quality delivery of projects in accordance with plant KPIs. Well organized and resourceful.     Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and

View the official posting →