ecrgrndonotaply-sendes2
Job Description
What you will do:
Research, design, develop, and verify innovative components and modules for medical devices with minimal supervision.
Translate customer needs and design inputs into engineering specifications and produce sub-system level designs.
Prototype and analyze design solutions to validate concepts and drive development decisions.
Apply fundamental and some advanced concepts, practices and procedures to solve complex technical challenges.
Ensure compliance with medical device regulations, design controls, risk management, and maintain thorough engineering documentation, such as the Design History file.
Collaborate cross-functionally with R&D, Quality, Manufacturing, Regulatory, Clinical, and Marketing teams to drive project success with minimal supervision.
Demonstrate strong ownership, prioritize tasks effectively, and contribute to a high-performing team environment under minimal supervision.
Build product knowledge, understand clinical applications, and develop awareness of financial modeling related to product development.
What you need:
Required:
Bachelor of Science degree in Engineering, Mechanical Engineering, or Biomedical Engineering or related discipline.
Minimum of 2 years of relevant work experience in mechanical engineering design and development.
Working knowledge and understanding of mechanical engineering practices and design principles.
Technical ability to create engineering drawings and models, applying GD&T and CAE tools
Preferred:
Proficiency with CAD tools (e.g., SolidWorks, Creo, or similar platforms).
Demonstrated ability to apply knowledge of materials and manufacturing processes to product design.
Experience working in a regulated industry (e.g., medical device, aerospace, automotive, or similar).
Ability to communicate basic plans and technical information clearly to team members.
Company Information
Location: Portage, MI
Type: Hybrid