Careers with GyroGear™

GyroGear™ is the innovation-driven, award-winning creator of the GyroGlove™.
We are a focused yet flexible team, comprising individuals that care about changing the world through innovations.

Who We Need

GyroGear™ seeks high-impact team players who will contribute to a vibrant company culture. They must work well with people from a variety of backgrounds and cultures, and be able to manage a dynamic workload across different disciplines.
If you are driven, have an insatiable curiosity and desire to innovate, excellent communications skills, and can easily interface with both corporations and consumers, reach out to us.

What We Offer

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International work experience

Join a team of the best and the most talented minds from all over the world, working together to overcome contemporary problems with cutting-edge technology

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Competitive remuneration

We offer a competitive salary with a reward system based on quality, not quantity. Regular reviews ensure we treat each other fairly.

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Innovative atmosphere

Building an innovative product requires innovative people. Regardless of our core disciplines, each team member deeply understands the logic behind every department’s strategy and science, and is encouraged to question and help construct the product at each step.

Electronics Technician

• Minimum 5 years of experience in the design and development of electrical systems, ideally within a medical industry, but candidates from other industries are still welcome.
• High proficiency at soldering, PCB construction and surface-mount PCB assembly.
• Knowledge of electronics (analog/digital) and test equipment knowledge helpful.
• Familiar with electromechanical assemblies: motors, sensors, PCBA’s, buttons, etc.
• Knowledge of embedded software development and debugging.
Send us your CV and a cover letter to

Job Specs

Quality and Regulatory Affairs Manager

• 5-10 years of relevant work experience in medical device development, with at least 5 years in a leading QA/RA position.
• Knowledge and working experience of quality management system, standards and government regulations applicable to medical devices e.g. ISO 13485, 21 CFR 820 QSR, MDD 93/42/EEC.
• Experience in completing submissions to FDA, EU regulatory entities and creating/maintaining product EU technical files.
Send us your CV and a cover letter to

Job Specs


Interested in joining a focused, dedicated team putting across quality products for neurological conditions?
Send us your CV and a cover letter at the address below.

Apply now