We are looking for a highly motivated and experienced Senior Verification Engineer to perform and guide design verification for the electro-mechanical portions of the system design.

For this role, we’re focusing on electrical and mechanical parts, assembly and functional aspects of the system design. This is an ideal opportunity for someone who is motivated and passionate to make an impact in leading the development of the next generation of ophthalmic robotic surgery.

We are here to improve lives by restoring sight worldwide by a robotic platform for vision saving surgery. Our company will improve the way ophthalmic surgery is delivered to vision impaired individuals now and for decades to come.

We are rapidly growing, funded by leading international VCs, and are looking to expand our small, motivated, multi-disciplinary and phenomenal team. Joining us is an opportunity to work towards saving vision across the globe, collaborating with others to realize a dream, and tackle an enormous challenge that will help drive your career forward.

• Create verification protocols based on electromechanical design input requirements.
• Identify applicable standards for each electromechanical aspect and define how they are addressed in verification activities.
• Establish statistical sample sizes according to the risk level associated with each part, assembly, and feature.
• Lead protocol development and test execution for sterilization validation.
• Guide a team of verification engineers and testers in creating test protocols, executing tests, reviewing results, and generating reports.
• Participate as a team member in the development of new features related to electromechanical assemblies and associated robotic capabilities.

• BSc degree in Electrical or Mechanical, or Biomedical Engineering.
• 5+ years of experience in design verification of electrical, mechanical, and multi-disciplinary medical device systems.
• Experience with optical systems (e.g., imaging, illumination, lenses, cameras) in medical devices – an advantage.
• Proven experience in establishing and justifying statistical sample sizes for verification activities.
• Experience with sterilization processes and validation - an advantage.
• Familiarity with medical device standards and regulations, such as ISO 13485 and IEC 60601.
• Excellent verbal and written communication skills in English.
• Strong problem-solving abilities, attention to detail, and the ability to quickly learn new technologies and systems.