Qualifications
Bachelor's degree in Life Sciences, Engineering, or a related field.A minimum of 5 years of experience in regulatory affairs within the medical device industry.Strong knowledge of FDA regulations and international standards (ISO 13485, MDR).Excellent communication and analytical skills.Ability to work collaboratively in a fast-paced environment.
About the job
Join Intuitive Surgical, a leader in robotic-assisted surgical technology, as a Regulatory Affairs Specialist 3 for the Multiport da Vinci system. Your expertise will be crucial in navigating the complex regulatory landscape and ensuring compliance with FDA and international regulations.
In this role, you will collaborate with cross-functional teams to support product development, regulatory submissions, and post-market surveillance activities. Your insights will help shape the future of surgical innovation, making a significant impact on patient outcomes.
About Intuitive Surgical, Inc.
Intuitive Surgical, Inc. is dedicated to revolutionizing surgery with its innovative robotic systems. Our da Vinci surgical platform has transformed minimally invasive surgery, allowing for greater precision and improved patient outcomes. Join our passionate team and be part of a company that is changing the landscape of healthcare.