Cork, Ireland
25 days ago
Engineer/ Senior Project Engineer, PSE
Work Flexibility: Hybrid or Onsite

Engineer/ Senior Engineer - Product Support Engineering

Anngrove or Limerick

Position Summary

This is an exciting engineering opportunity within the Joint Replacement Product Support Engineering team. This is a hybrid role, offering great flexibility to work-from-home and work on-site across multiple facilities in the Stryker Ireland campus. As a Project Engineer, you will be part of a global team with multi-site responsibilities sustaining our world class hip and knee replacement devices (implants and instruments). You will partner with our cross-functional colleagues (manufacturing, quality, regulatory, design assurance & clinical) to support a diversity of challenges, including; product design updates, design-for-manufacturability activities, tolerance analysis/stack-ups, prototyping, design control updates, regulatory body submissions, manufacturing transfers and more!  

What you will do: 

Work on cross-functional teams to address design and manufacturing changes and maintain existing designs. Become an expert in product knowledge for our hip and knee implant/instrument portfolio.  Perform tolerance analysis, research legacy testing & design controls and draft technical protocols/reports/assessments to maintain and sustain our Joint Replacement (hip and knee) product portfolio Update/remediate design control documents to comply with General Safety and Performance Requirements. Model and detail implant and instrument designs utilizing Pro/Engineer design software.  Utilize knowledge of the surgical procedure to develop innovative solutions to solve & satisfy customer needs. Collaborate with our manufacturing partners to troubleshoot and resolve challenges associated with supply of our product to the market Support FDA and world-wide submissions through design rationales and compliance to industry standards with an international team. 

What you need: 

Level 8 Degree in a science or engineering discipline. Mechanical or Biomedical preferred. 0+ years of experience Experience in medical device industry or other regulated industry preferred. Excellent presentation and written / verbal communication skills Ability to read detailed engineering drawings and understand basic GD&T tolerancing principles to the ASME Y14.5 (or equivalent) standard.  Be a positive, energetic team player, and an advocate for product excellence and quality. Capable of working as part of a multi-disciplined team in a dynamic and results motivated environment Strong organizational, interpersonal, communication and influencing skills. High level of PC skills. Must be proficient with Microsoft applications (Outlook, Word, Excel, PowerPoint, etc.) and CAD package (Creo/Pro-Engineer preferred). 

Travel Percentage: 10%

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