Staff Engineer

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

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

What you will need-
Required Skills :
• Bachelor of Science in Engineering, Mechanical Engineering & 6-9 years of work experience

• Strong technical ability to develop and optimize designs for mechanical / electro-mechanical assemblies incorporating DFM principles; creating engineering drawings, models, applying GD&T and CAE tool.

• 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.

Preferred Qualifications:

• Adept at applying knowledge of materials and manufacturing processes to product design and ability to communicate moderate complexity plans and technical information to team members

• Good working knowledge of CAD applications (Creo/SolidWorks/UniGraphics)

• 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%