Design Engineer

Stryker Corporation

Carrigtwohill

Hybride

EUR 40 000 - 67 000

Plein temps

Il y a 2 jours
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Résumé du poste

Stryker Ireland is seeking a graduate or early-career engineer to support post-market design activities across multiple medical devices. Based in Ireland, you will investigate customer complaints, perform root cause analyses, and collaborate with Quality, Marketing, Operations and Regulatory Affairs to drive design improvements.

You will gain hands-on experience in product design, verification and validation, CAPA and ECR processes, and learn medical device design controls while contributing to

Qualifications

  • Bachelor's degree in a relevant engineering discipline.
  • Internship or project experience is advantageous but not required.
  • Strong analytical and problem-solving skills.
  • Ability to work effectively with cross-functional teams and communicate technical information clearly.
  • Organised and detail-oriented, with the ability to manage multiple activities and maintain accurate documentation.
  • Willingness to learn medical device design controls, risk management, verification testing and post-market engineering processes.

Responsabilités

  • Support post-market design activities for commercially released medical devices, helping to ensure products continue to meet customer, quality and regulatory requirements.
  • Investigate customer complaints, field returns and product performance issues using structured problem-solving and root cause analysis techniques.
  • Partner with Quality, Marketing, Operations and Regulatory Affairs to identify opportunities for product improvements and support implementation of design changes.
  • Plan and execute engineering testing, verification and validation activities to evaluate product performance and support proposed design improvements.
  • Support Nonconformance (NC), Corrective and Preventive Action (CAPA), and Engineering Change Request (ECR) activities while maintaining compliant engineering documentation.
  • Develop a deep understanding of Stryker products through real-world engineering challenges, building expertise in product design, manufacturing, customer use and post-market performance while helping drive product improvements and influencing future product designs.

Connaissances

Mechanical Engineering
Biomedical Engineering
Manufacturing Engineering
Electrical Engineering
Materials Science
Problem solving
Cross-functional teamwork
Technical communication

Formation

Engineering degree ( Mechanical / Biomedical / Manufacturing / Electrical / Materials Science )

Description du poste

Work Flexibility

Hybrid Position summary: This role will support a wide range of products across multiple surgical specialties, with a primary focus on post-market design support and product performance. Working closely with Quality, Marketing, Operations and Regulatory Affairs, you will investigate customer complaints, field returns and product performance trends to identify opportunities for improvement and support implementation of design changes. Product Engineering offers a unique opportunity to learn how medical devices perform throughout their entire lifecycle. You will develop deep product knowledge by working on real-world engineering challenges, gaining firsthand experience of how products are designed, manufactured, used by customers and perform in the field. Through investigation of product issues and implementation of improvements, you will help enhance product quality, reliability and customer experience, while contributing valuable insights that influence future product enhancements and next-generation designs.

What you will do:
  • Support post-market design activities for commercially released medical devices, helping to ensure products continue to meet customer, quality and regulatory requirements.
  • Investigate customer complaints, field returns and product performance issues using structured problem-solving and root cause analysis techniques.
  • Partner with Quality, Marketing, Operations and Regulatory Affairs to identify opportunities for product improvements and support implementation of design changes.
  • Plan and execute engineering testing, verification and validation activities to evaluate product performance and support proposed design improvements.
  • Support Nonconformance (NC), Corrective and Preventive Action (CAPA), and Engineering Change Request (ECR) activities while maintaining compliant engineering documentation.
  • Develop a deep understanding of Stryker products through real-world engineering challenges, building expertise in product design, manufacturing, customer use and post-market performance while helping drive product improvements and influencing future product designs.
What you will need:
  • L8 Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, Electrical Engineering, Materials Science or related engineering discipline.
  • Relevant internship, co-op, university project or research experience is advantageous but not required.
  • Strong analytical and problem-solving skills with an interest in understanding how products fail and how they can be improved.
  • Ability to work effectively with cross-functional teams and communicate technical information clearly.
  • Organised and detail-oriented, with the ability to manage multiple activities and maintain accurate documentation.
  • A willingness to learn medical device design controls, risk management, verification testing and post-market engineering processes.
Who we want:
  • Curious problem solvers – People who enjoy understanding how products work, investigating problems and identifying root causes.
  • Eager learners – Individuals who seek feedback, continuously develop their technical knowledge and are excited to build expertise in medical device engineering.
  • Team players – Engineers who collaborate effectively across Quality, Operations, Regulatory Affairs, Marketing and Product Engineering.
  • Detail-oriented thinkers – People who can analyse data, identify trends and document technical work accurately in a regulated environment.
  • Self-motivated contributors – Individuals who take ownership of their work and proactively drive actions to completion.
Salary Range:

#IJ Salary Range: 40,000.00 - 67,000.00 EUR Annual

Travel Percentage: 10%

At Stryker, we believe transparency helps candidates make confident decisions about their next career step. Compensation is an important part of that process and we want to be clear about how pay is determined. The compensation information posted for this role may be presented as a salary range or a fixed amount depending on the role. In addition to base salary, this role may be eligible for incentive compensation (such as bonus and/or commissions where applicable), along with Stryker's comprehensive benefits package.

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

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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