Company Description

Endovision helps to improve the diagnostic accuracy of upper GI endoscopists and saves their time, enabling them to perform better and faster using deep learning and computational modeling.

Role Description

This is a full-time on-site role located in New Delhi for a QA Intern (Medical Device) at Endovision. The QA Intern will be responsible for day-to-day quality assurance tasks related to medical devices.

• Support the maintenance and organization of the Quality Management System (QMS) in compliance with ISO 13485.
• Assist in document creation, formatting, review, approval, and distribution processes.
• Ensure document control procedures are adhered to, including version control, archival, and retrieval.
• Monitor and manage the document review and revision schedule.
• Participate in internal audits to verify document control compliance.
• Collaborate with cross-functional teams to ensure document access and compliance awareness.
• Help in updating quality manuals, SOPs, and records to meet current standards and regulations.

Qualifications

• Knowledge of quality assurance processes and procedures
• Understanding of medical device regulations and standards
• Excellent attention to detail and analytical skills
• Strong communication and teamwork abilities
• Pursuing or completed a degree in a relevant field (e.g., Biotechnology, Biomedical Engineering, Quality Assurance or related field)