Job description
Work Flexibility: Hybrid What you will do:
- Under supervision, design, develop, modify, and verify mechanical components for medical devices
- Assist with prototyping and bench testing
- Support problem solving, root cause analysis, identify potential solutions, and evaluate them against requirements
- Under supervision, conduct research and studies to support product design
- Interpret customer needs and understands design inputs
- Understand the product’s intended use and clinical procedures
- Understand fundamental industry standards, design requirements and test strategies which align with regulatory requirements
- With supervision, create or refine engineering documentation, such as the Design History file per company design control procedures
- Learn R&D procedures like design controls and risk management, per the Quality Management System
- With supervision, work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success
- Learn procedures, policies, processes, systems, and technology required
- Work on problems in limited scope; purposefully learn while gaining experience
- Demonstrate ownership and integrity of work
- Build stable relationships
- Contribute to the project as a team member What you will need: Minimum Qualifications (Required):
- Bachelor of Science in Engineering, Mechanical Engineering or Bio. Medical & 8+ years of work experience Preferred Qualifications (Strongly desired):
- Fundamental knowledge and understanding of mechanical engineering practices and tools, design principles within a regulated environment.
- Basic knowledge of design and concept generation CAD or CAE modeling tools
- Basic knowledge of analysis tools and statistical methods
- Basic knowledge of materials and manufacturing methods
- Ability to read and Interpret complex drawings Travel Percentage: 30%