|| Who we are

At TWIICE, we believe that life should be accessible to all. This is why we develop exoskeletons that give people the freedom to do what they love.

As a leader in wearable robotics, we keep pushing the boundaries of technology for the benefit of human beings. Fundamentally user-centered, we work everyday towards ever more inclusion through ethical technology.

|| Position

You will be responsible for ensuring our compliance with regulatory requirements in the field of medical robotics. You will also oversee the Quality system deployment, maintenance, and compliance throughout the company, as required by the regulatory requirements of the countries operated.

The ideal candidate will have at least 3 years of experience in the medical device field, with knowledge of the CE-marking or FDA approval processes.

Responsibilities and Duties

• Take overall responsibility for Quality and Regulatory Affairs within the company
• Drive certification processes and documentation compliance
• Assist with Quality Management System deployment, maintenance, and compliance throughout the company
• Drive compliance of operations and auditability as per internal and/or external requirements.
• Drive internal training on regulatory requirements, quality processes and applicable standards

This position is 50% initially but will increase in the next 12 months, and we are looking for a candidate who can commit to growing with the company. We offer flexible working conditions and participation in the employee stock option plan.

|| About you