We are a young and dynamic startup that is working hard to bring eye screening to everyone.

We are hiring, so please reach out to us if you believe in our mission and think you are the right fit!

We are looking for a Quality Assurance & Regulatory Affairs (QARA) professional with 1–3 years of experience in the medical device industry. The candidate will support the maintenance of the Quality Management System (QMS), regulatory documentation, technical documentation, and compliance activities in accordance with applicable regulatory requirements and standards.

Key Responsibilities
Quality Management System (QMS)

• Maintain and support the company’s Quality Management System in compliance with International Organization for Standardization 13485 requirements.

• Prepare, review, update, and maintain QMS documents including SOPs, procedures, work instructions, forms, and templates.

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