Sr. Design Engineer na Tyber Medical LLC

Description

Develop new medical devices and/or make enhancements to existing products through regular interaction with a cross-functional team.  The Sr. Design Engineer must also assist with relevant development processes and conform to the guidelines described in the company’s quality system and other policies.    

Requirements

Primary Job Responsibilities: 

• Research and develop surgical implants and instruments in accordance with regulatory and quality requirements. 
• Create 3D part files and 2D technical drawings using SolidWorks. 
• Analyze test data and generate reports to verify or validate that designs meet functional and performance specifications. 
• Interact and coordinate with other departments to establish project plans, product requirements, and other documentation activities in accordance with design control and risk management procedures. 
• Provide assistance to the Manufacturing, Supply Chain, Quality and Regulatory departments as needed. 
• Interface with suppliers and provide support during the manufacturing process. 
• Follow organizational and group guidelines, procedures, protocols. 
• View surgical procedures in operating room or cadaver lab. 
• Present and share information with management, customers, and/or field personnel when requested (PowerPoint skills preferred). 
• Independently lead/execute project deliverables and manage multiple tasks at once. 
• Promote and ensure continual improvement in all interacting departments. 
• Communicate effectively to ensure project team and senior management are aware of upcoming milestones and risks/issues. 

Secondary Job Responsibilities: 

• Inspect inventory components and supervise first product builds 
• Support business development and management activities 
• Participate in research assignments including trade show and other conference attendance 
• Respond to field questions related to products and projects when necessary  

Educational Requirements:  BS in engineering (mechanical and/or biomedical a plus) or equivalent work experience. 

Experience Requirements: 2-years product development experience in medical device desired. 

Reports to: Sr. Project Engineer or equivalent