Senior Project Engineer - Sustaining
Publication date:
03 September 2024Workload:
100%Contract type:
Unlimited employment- Place of work:Memphis
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