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- Memphis, TN 37501, United States
- Jackson, TN, United States
- Nashville, TN, United States
Job details
Work flexiblity: Hybrid or Onsite
Req ID: R525709
Employee type: Full Time
Job category: Engineering
Travel: 10%
Relocation: Yes
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Why join Stryker?
We are excited to be named one of the World’s Best Workplaces by Fortune Magazine! We are proud to offer you 12 paid holidays annually. For an overview of our benefits and time off, please follow this link to learn more:US Stryker employee benefits.Job description
Stryker’s Global Product Engineering team is hiring a Senior Project Engineer to support a portfolio of recently acquired soft tissue fixation products that will enhance our ability to meet the diverse needs of our customers within the Stryker Trauma and Extremities Division. As a cross functional team member, you will maintain and improve our high standard in design specification and product performance throughout the product life cycle.
Who we want:
- Self-directed Initiators. People who take ownership of their work and need no prompting to drive productivity, change, and outcomes.
- Analytical problem solvers. People who seek to identify root causes, evaluate optimal solutions, and recommend comprehensive upgrades to prevent future issues.
- Collaborative Partners. People who build and leverage cross-functional relationships to bring together ideas, information, use cases, and industry analyses to develop best practices.
What you will do:
- As a member of the Global Product Engineering team, you will gain in-depth knowledge of Stryker’s Trauma & Extremities portfolio, including Soft Tissue Fixation, Intramedullary Nails, External Fixators, Bone Plates & Screws, Surgical Instruments, and other products that enhance people's lives.
- You will help maintain and improve our high standards in design specifications and performance for over 50,000 articles.
- You will oversee continuous improvement projects for existing products, manage project plans, and track work packages.
- You will participate in and occasionally lead cross-functional teams to address design-related Non-Conformities (NC) and Corrective- and Preventive-Actions (CAPA).
- You will ensure design requirements are met, apply the design change process, and identify technical solutions within your scope.
- You will work with Regulatory Affairs, Technical Publications, Design Quality, and Marketing to address design-related questions for international registrations and create technical files for EU-MDR compliance.
What you need:
Required
- Bachelor’s degree in engineering, mechanical engineering, or biomedical engineering
- 2+ years of engineering experience in a highly regulated industry
Preferred
- Medical device industry experience
- Experience with resorbable material, textile engineering and or sterile packaging systems