Regulatory Affairs Co-op: Medical Devices (EU/US)

PowerToFly; Carrigtwohill; On-site; EUR 27,000 - 33,000; Full time

Benefits offered by this job

Mentorship program

Flexible working hours

Career development opportunities

Job summary

Stryker offers a cooperative placement based in Cork, Ireland, focusing on Quality and Regulatory Affairs within a regulated medical device environment. You will work with mentors and cross-functional teams to understand EU directives (93/42/EEC, 2017/745) and US regulatory requirements, applying basic knowledge to real-world documentation and processes.

You will be eligible if enrolled in an Irish or Northern Irish university and available for 6, 9, or 12 months.

Qualifications

• Enrolled at an Irish or Northern Irish university for the duration of the cooperative placement.
• Available for 6, 9 or 12 months – exact duration and start date to be discussed with Talent Acquisition
• Currently completing an Irish or Northern Irish university qualification in Engineering or Science or related courses.
• Self-motivated, flexible, hardworking and able to work in a dynamic, results oriented environment.

Responsibilities

• Identify a Quality/Regulatory Affairs improvement project with objectives, scope, milestones and evaluation.
• Communicate project updates and present at project review forums.
• Assist in developing regulatory procedures and best practices.
• Assist in preparing technical documentation and submission packages for regulatory agencies.
• Ensure compliance with Quality and Safety systems.
• Be a team player, dependable, punctual and proactive.

Skills

Team player

Multi-tasking

Analytical skills

Verbal and written communication

Punctual

Self-motivated

Flexibility

MS Office

Education

Engineering or Science degree

Tools

MS Office

Job description

Stryker offers a cooperative placement based in Cork, Ireland, focusing on Quality and Regulatory Affairs within a regulated medical device environment. You will work with mentors and cross-functional teams to understand EU directives (93/42/EEC, 2017/745) and US regulatory requirements, applying basic knowledge to real-world documentation and processes.

You will be eligible if enrolled in an Irish or Northern Irish university and available for 6, 9, or 12 months.