Open Position – Senior Quality Engineer Horizon Surgical Systems Inc. Horizon Surgical Systems Inc. is revolutionizing the world of surgical ophthalmology by developing a novel, AI driven, and imaging-guided surgical robotic system.

Horizon Surgical Systems Inc. aims to expand access to care, provide superior capabilities to the human surgeon, and enhance patient outcomes. Microsurgery in general and Ophthalmology are subfields of surgery for which the surgical outcomes can be significantly improved by robotic systems to allow superior dexterity, precision, accuracy, and visualization beyond the human surgeon’s own capabilities.

We are seeking highly motivated, and intellectually inquisitive individuals looking to make a positive impact on healthcare via the development of robotic technology. The core values of Horizon Surgical Systems Inc. are: Commitment to Excellence: We aim to deliver superior patient outcomes and surgeon experiences Passion for Creativity and Innovation: We are driven by new ideas and aim to push the boundaries of what's possible Teamwork and Camaraderie : We achieve our best when we collaborate and work together Welcoming of Critical Opinion: We are enriched by constructive criticism and support the best ideas Personal Accountability: We honor our commitments and take responsibility for our actions Horizon Surgical Systems Inc.

offers: An opportunity to build autonomous surgical robotic systems driven by image guidance and AI technology for the future of affordable, high-quality healthcare. The opportunity to work alongside clinicians, engineers, and global leaders in cutting-edge AI, imaging, and robotics technology.

Compensation

and an excellent company-paid

Benefits

package.

Requirements

. As a senior member of our team, you will provide quality engineering support in the design, development, and manufacturing of Horizon products to ensure that the products conform to established specifications and consistently meet or exceed the

of our customer and patients.

at all phases of product/process development and manufacturing. Work with Product Development on product V V activities including sterilization, packaging/labeling, transit testing, real time/accelerated aging as well as creation of protocols and reports. Work with Product Development on the Risk Management Process and maintains the Risk Management File.

Responsible for the Design History File, device Master Record and its maintenance. Responsible for setting up the receiving inspection area, perform materials inspection such as incoming, First Article Inspection, and final product release. Responsible for documenting product discrepancies and follow up on NC implementation and closure.

Responsible for all supplier management activities including sourcing and qualifying suppliers, maintaining the Approved Suppliers List (ASL) and associated files, and managing the Supplier Corrective Action Request (SCAR) program. Responsible for CAPA management from CAPA generation to implementation of corrective action, verification of effectiveness, and closure. Assists with internal audits.

Assists with hosting external audits and drive all issues to closure if need be. Responsible for product packaging/labeling and ensuring all materials are conforming with applicable regulations. Other duties as assigned.

Responsibilities

Duties Works with Product Development and Operations teams to establish quality

Required Qualifications

BS degree in Engineering, life sciences or related field – Advanced degree preferred. 5 plus years experience as a Quality Engineer or in related field in the medical device Industry. ASQ CQE is a plus.

Experience with design control is a must. Experience with software and firmware V V is strongly preferred.