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Principal Mechanical Design Engineer

2 months ago


Brockton, Massachusetts, United States BAXTER Full time
About the Role

We are seeking a highly skilled Principal Mechanical Design Engineer to lead our product development team at Baxter. As a key member of our global hardware team, you will be responsible for designing and engineering innovative solutions for both legacy and new product development.

Key Responsibilities
  • Design new parts and assemblies using CAD software, generating CAD models, assemblies, and drawings from engineering requirements.

  • Create and lead processing change orders to release or modify existing mechanical models and drawings and bills of materials.

  • Apply principles of mechanics, thermodynamics, hydraulics, heat transfer, and materials, and confirm correctness using engineering methodologies and tools such as FEA, GD&T, etc.

  • Develop and complete documentation deliverables including design description reports, design models, drawings, and engineering analysis reports.

  • Work with suppliers, manufacturing, and service to design for manufacturability and serviceability.

  • Collaborate with test engineering to support creation of test protocols and reports for verification and validation testing.

  • Research and analyze design and experimental data to understand technical issues and set a direction for issue resolution.

  • Effectively communicate project technical status, time, and schedule for tasks, including estimates to complete.

  • Complete engineering tasks in a timely fashion and manage time budgets for tasks. Identify and efficiently resolve technical problems and issues.

Requirements
  • Bachelor's degree in Engineering, Mechanical preferred or equivalent.

  • Minimum 7+ years of experience in new product development, with at least one medical device project from concept to market introduction. Experience with IEC 60601-1 is a plus.

  • Direct experience with the product development process, from requirements development to prototyping, design for manufacturing, verification, and product release.

  • Experience in medical device or other regulated industries is preferred.