Regulatory Affairs Co-Op

Stryker

Belfast City District

Vor Ort

GBP 23.000 - 28.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Mentorship program
Flexible working hours
DE&I employee resource groups
Co-op networking with leaders
Sports & Social clubs

Zusammenfassung

Stryker is seeking a Regulatory Affairs & Compliance Engineering Co-op based in Belfast. You will gain hands-on experience across the department, supporting product registrations, change management, and Eudamed, while working with mentors to enhance your growth and confidence.

The role offers flexible hours, a people-first culture, and opportunities to contribute to real-world healthcare projects within a leading medical technology company.

Qualifikationen

  • Undergrad in Biomedical Engineering or equivalent degree.
  • Co-op role to learn regulatory product requirements (FDA, MDR, TGA).
  • Assist in designing and developing tools to enable decision making and data input.

Aufgaben

  • Gain experience across the department by learning regulatory product requirements and supporting registrations, change management, technical files and Eudamed.
  • Support regulatory affairs by designing and improving tools to boost efficiency and data analysis.

Kenntnisse

Regulatory affairs

Ausbildung

Biomedical Engineering

Tools

Eudamed

Jobbeschreibung

Work Flexibility: Onsite

This role will be based in our Belfast site.

Regulatory Affairs & Compliance Engineering

Stryker HeartSine AED Regulatory Affairs & Compliance Engineering maintain market access for AED and Pad-Pak products through product registration, develop regulatory strategies for new product development and change management, liaise with regulatory notified bodies and are responsible for change submissions.

Tasks and Responsibilities
  • As a Co-Op you will gain experience across the department, learning the market regulatory product requirements (eg FDA, MDR, TGA) Stryker systems and supporting our specialists with product registrations, change management, technical file and Eudamed.
  • Supporting the regulatory affairs function with designing, improving and developing tools which enable efficiency for both decision making, data input and analysis.
What you will need
  • Undergraduate in Biomedical Engineering or equivalent degree course.
What we can offer
  • Attractive salary & vacation entitlement.
  • Experience our inclusive, people-first culture.
  • You will be paired with mentors and have access to leaders who support your growth, give constructive feedback, and help build confidence.
  • Flexible working hours.
  • Sports & Social clubs and DE&I Employee Resource Groups and the opportunity to connect with other co-ops.
  • The opportunity to contribute to real-world projects that make a difference in improving healthcare and patients’ lives.
  • In Stryker, you will be given responsibilities that truly matter.

Belfast: £25,000 GBP Annual

Travel Percentage: None

About Stryker

Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces! For more information, visit: www.stryker.com

Work Flexibility Options
  • Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location.
  • Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based.
  • Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category.
  • Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.
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