Work Flexibility: Hybrid

What you will do:

Technical Responsibilities:

• 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

• Working on multiple projects simultaneously in product engineering such as gap assessments, design changes, manufacturing transfers, product development, regulatory or business-driven projects, etc.

• Execution of NC CAPA implement design controls & risk controls.

Experience in executing NPD projects involving the complete product development life cycle phases from concept to launch.

Business Responsibilities:

• Advance solutions by applying in-depth knowledge of customer needs, market and competitive offerings
• Apply detailed knowledge of clinical procedures to author design inputs
• Support Voice of Customer sessions internally and with clinicians. Demonstrate developing financial acumen

Med Device Compliance:

• 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

General Responsibilities:

• Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success
• Identify and support the creation of or improvements to procedures, policies, processes, systems, and technology. 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. Collaborate with cross-functional teams to build partnership to achieve business objectives

Minimum Qualifications (Required):

• Bachelor of Science in Engineering, Mechanical Engineering & 6-9 years of work experience

Preferred Qualifications (Strongly desired):

Technical Skills:

• 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

• Good working knowledge of CAD applications (Creo/Solid Works/Uni Graphics)

• Experience with analysis tools, specifically tolerance analysis, CFD and FEA using ANSYS software preferred. Competency in statistics, process capability, design of experiments, including statistical applications such as Minitab, etc.

• Experience in working with regulated industries like Medical devices, Aerospace, Automotive etc. Understanding of medical device standards and regulations is preferred. Good understanding of designing of jigs & fixtures and inspection methods.

Travel Percentage: 10%