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).