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R&D Project Manager- Medical Exoskeleton Devices

Full Time

About The Role

As an R&D Project Manager for Medical Exoskeleton Devices, you will lead a team of researchers and engineers in the development of innovative medical exoskeletons/robots. You will be responsible for overseeing the entire research and development process, from concept to commercialization, and ensuring that the project is completed within the allocated budget and timeline.


  • Lead the research and development process for medical exoskeleton/robotic devices, from concept to commercialization, while managing the project budget and timeline.
  • Work closely with cross-functional teams including Regulatory, Quality, Marketing, and Manufacturing to ensure compliance with regulatory requirements, customer needs, and scalability.
  • Identify project risks, develop mitigation plans, and communicate progress to key stakeholders, providing regular project updates to management and other stakeholders.
  • Ensure designs and development processes meet applicable standards, like ISO 13485, FDA regulations, and other relevant standards by conducting technical reviews of product designs and engineering changes to ensure compliance with necessary standards and specifications.
  • Foster a culture of innovation within the R&D team, encouraging the development of new ideas and creative solutions to complex problems.
  • Work with legal counsel and management to develop intellectual property strategies,
  • managing the company's intellectual property portfolio related to medical exoskeleton devices, including patent filings and maintenance.
  • Building a team to fulfil the project requirement.
  • Stay up-to-date on industry trends and emerging technologies related to medical exoskeleton devices, ensuring the company remains competitive and innovative.

Required Qualifications

  • Bachelor’s or Master’s degree in Biomedical Engineering, Mechanical Engineering, or related field.

Required Skill Sets

  • Team management.
  • Strong technical background.
  • Knowledge of regulatory requirements for medical devices and experience working with regulatory bodies.
  • Experience with product development processes including design control, risk management, and verification and validation.
  • Ability to work in a fast-paced, dynamic environment with changing priorities and timeline.
5-7 Years Experience Required
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