Don’t send a generic resume — generate a resume and cover letter tailored to this exact role.
Stryker in Cork offers a cooperative placement in Quality/Regulatory Affairs within a regulated medical device environment. You will gain exposure to EU MDR, US regulatory requirements, and develop skills in regulatory procedures and documentation under mentorship.
You will contribute to real-world healthcare improvements while working with a multi-disciplinary team and leaders who support your growth.
This role will be based in one of our Cork sites.
Throughout the placement, you will be an integral part of Stryker’s 2027 Cooperative cohort.
This position provides experience of working in a regulated medical device company. You will have the opportunity to develop and apply basic knowledge and understanding of the quality, regulatory and legal frameworks, regulatory requirements, legislation, processes and procedures.
Additionally, this opportunity provides good knowledge of EU Medical Device Directive 93/42/EEC, EU Medical Device Regulation 2017/745 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.
Tasks and responsibilities may include:
Ireland: €30,000 EUR Annual
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.