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TAS Medical, Inc. in San Carlos, CA is seeking a senior Mechanical Design Engineer to lead the design and development of laparoscopic surgical devices and assemblies for tissue approximation products.
This full-time, on-site role involves creating and refining product concepts, CAD modeling, and supporting prototype build and testing. You will collaborate with R&D, quality, manufacturing, and regulatory teams to ensure compliance with medical device standards and participate in design reviews,
TAS Medical, Inc. is dedicated to improving surgical outcomes by reducing wound dehiscence and enabling more minimally invasive procedures. The company’s mission is to save lives, shorten hospital stays, and reduce healthcare costs by hundreds of millions of dollars each year. TAS Medical has developed a minimally invasive tissue approximation kit that uses medical-grade zip-ties to quickly and effectively approximate soft tissue in a wide range of high-volume surgical procedures. This solution is backed by strong intellectual property, positioning the company as an innovator in surgical device technology. Team members contribute directly to advancing simple, effective tools that support surgeons and patients worldwide.
The Sr. Mechanical Design Engineer – Medical Device will lead the design and development of laparoscopic surgical devices and assemblies for TAS Medical’s tissue approximation products. This full-time, on-site role in San Carlos, CA involves creating and refining product concepts, performing detailed mechanical analyses, and translating clinical requirements into robust, manufacturable designs. Day-to-day responsibilities include developing CAD models and drawings, evaluating materials and mechanisms, collaborating with cross-functional teams (R&D, quality, manufacturing, and regulatory), and supporting prototype build, testing, and design iterations. The engineer will participate in design reviews, apply design-for-manufacturability principles, and ensure compliance with medical device standards and quality systems. This role also contributes to continuous improvement of existing products and supports documentation needed for verification, validation, and regulatory submissions.