Description This position provides experience of working in a regulated medical device company.
You will have the opportunity to enhance team productivity and efficiency through automation in multiple high-impact areas, while also providing a valuable learning opportunity.
Additionally, this opportunity provides good knowledge of EU Medical Device Directive *****/EEC, EU Medical Device Regulation ******** and US regulatory requirements across a wide range and classification of products.
Through this, it is possible to see how these regulations are implemented in practice in industry.
Throughout the placement, you will be an integral part of Stryker's **** Cooperative cohort.
Together, with your Stryker team leader and college supervisor, identify a Quality/Regulatory Affairs improvement project along with project objectives, scope, success factors, milestones and evaluation Maintain and enhance CHD automation systems Developing a prototype AI chatbot to assist engineers and technicians in accessing technical documentation and troubleshooting steps.
Enhance and centralize Power BI dashboards; build a backlog of reports supporting complaint trends and performance metrics.
What you will need: Currently completing an Irish or Northern Irish university qualification in Engineering, Science, Data Analytics or other related courses Honesty and integrity ; must comply with the quality system, regulations, and company policies Self-motivated, flexible, and hardworking - enjoys working in a dynamic, fast and results orientated environment Reliable, dependable, and punctual Organised, focused, and capable of multi-tasking Good analytical and problem-solving skills Good verbal and written communication skills as well as basic PC skills Is a team player and capable of working as part of a multi-disciplined team What we can offer : Attractive salary