Work Flexibility: Hybrid
What you will do:
Independently research, design, develop, modify, and verify components, modules and sub-systems for medical devices
Translate user needs to design inputs/specifications and produce complex system level designs with some guidance
Conduct or design advanced prototyping and testing; analyze and correct complex product design issues using independent judgment
Apply detailed knowledge of clinical procedures to author design inputs and support Voice of Customer sessions internally and with clinicians
Be proficient with and mentor others in usage of industry standards, including design requirements and test strategies per applicable regulations
Lead creation and refinement of engineering documentation, such as the Design History file
Follow and mentor others on R&D procedures like design controls and risk management, per the Quality Management System
Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success
Support and execute segments of complex multifunctional teams to advance projects through the design/development/launch process
Deliver high quality results with passion, energy and drive to meet business priorities and collaborate with cross-functional teams to build partnership to achieve business objectives
Minimum Qualifications
Required:
Bachelor of Science in Engineering, Mechanical Engineering or BioMedical
Work experience- 7 years -10 years
Preferred Qualifications:
Strong technical ability to develop and optimize designs for mechanical/electro-mechanical assemblies incorporating DFM principles
Strong technical ability in creating engineering drawings, models, applying GD&T and CAE tool
Adept at applying knowledge of materials and manufacturing processes to product design
Ability to communicate moderate complexity plans and technical information to team members
Travel Percentage: 10%