Research And Development Engineer

2 weeks ago

Minnetonka, United States Intellectt Inc Full time

Hello,

One of my clients is looking Role: R&D Engineer, if you’re interested or your skills matches, please share with me your updated resume to sushma@intellectt.com


Job Title: R&D Engineer

Location: Minnetonka, MN

Duration: 12 Months

Shift: 8:00 AM to 5:00 PM


Position Overview:

The R&D Engineer will support product development by performing clinical-systems and human factors engineering tasks. This includes investigating, defining, analyzing, documenting, and testing activities to contribute to the successful development of medical device projects. The role requires a solid understanding of engineering principles, clinical requirements, and marketing needs to address technical challenges effectively.

Key Responsibilities:

  • Product Development Support:
  • Collaborate with cross-functional teams to support clinical-systems and human factors engineering tasks.
  • Investigate and define technical requirements and constraints for assigned system components.
  • Perform analysis and conduct interviews to gather system requirements.
  • Technical Problem-Solving:
  • Apply engineering and scientific principles to evaluate and resolve technical issues.
  • Exercise technical judgment to plan, organize, and execute clinical-systems engineering assignments.
  • Utilize creative and analytical techniques to develop solutions within project constraints.
  • Documentation and Testing:
  • Document technical findings, system requirements, and design considerations.
  • Conduct testing activities to ensure compliance with engineering standards and project specifications.
  • Cost Efficiency and Best Practices:
  • Implement the most effective, cost-efficient methods to execute processes.
  • Ensure adherence to industry best practices for engineering and design.
  • Cross-Functional Collaboration:
  • Integrate technical, clinical, and marketing perspectives to resolve project-related tasks.
  • Work under general supervision, demonstrating the ability to manage multiple priorities within assigned projects.

Required Qualifications:

  • Education:
  • Bachelor's degree or higher in Engineering, Systems Engineering, Biomedical Engineering, or a related field.
  • Experience:
  • 2-4 years of experience in clinical-systems engineering, human factors engineering, or related roles within product development.
  • Familiarity with the medical device industry and regulatory standards is preferred.
  • Technical Skills:
  • Strong analytical and problem-solving skills with the ability to apply theoretical principles to practical challenges.
  • Proficiency in documenting system requirements and conducting technical analyses.
  • Knowledge of human factors engineering and clinical systems design is a plus.
  • Soft Skills:
  • Excellent written and verbal communication skills.
  • Ability to work collaboratively with cross-functional teams.
  • Strong organizational skills with the ability to manage multiple tasks effectively.

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