ecrgrndonotaply-sendes2

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.