Systems Verification Engineer

Johnson & Johnson Innovative MedicineSanta Clara, CA
23h$87,000 - $140,300Onsite

About The Position

Auris Health Inc., a member of Johnson & Johnson's Family of Companies, is currently recruiting for a Systems Verification Engineer, located in Santa Clara, CA. Robotics & Digital Solutions, part of the Johnson & Johnson family of companies, is Recruiting for a Systems Verification Engineer, located Santa Clara, CA. Robotics & Digital Solutions is part of Ethicon, Inc., a global leader in surgery with products and solutions found in almost every operating room around the world. Ethicon has made significant contributions to surgery for more than 100 years from creating the first sutures, to revolutionizing surgery with minimally invasive procedures. Our continuing dedication to Shape the Future of Surgery is built on our commitment to help address the world's most pressing health care issues and improve and save more lives. Through Ethicon's surgical technologies and solutions including robotics, digital solutions, sutures, staplers, energy devices, trocars and hemostats and our commitment to treat serious medical conditions like obesity and cancer worldwide, we deliver innovation to make a life-changing impact. For more information, visit www.ethicon.com. The Systems Verification Engineer will own, manage, and develop test equipment and systems for the Johnson & Johnson Surgical Robotics system. The individual should have strong communication skills as they will work closely with engineers from all functional teams; including R&D, systems, quality engineering, and external vendors. The engineer will document the test equipment and systems in accordance with FDA design control processes (21 CFR820.30) and IEC 62304.

Requirements

  • B.S. in Engineering or other applicable technical degree
  • Highly organized; strong project management ability and communication skills
  • Experience in test system design, implementation, manufacturing, and qualification/maintenance is preferred.
  • Medical device or similar regulated industry (e.g. automotive, aerospace)experience is preferred
  • Possesses breadth of knowledge across engineering fields (Electrical, Mechanical, Software), with domain expertise in at least one area is required.
  • Proficient in technical writing and good documentation practices is required.
  • Experience developing and executing test method validation and equipment qualification is preferred
  • Robotics or electro-mechanical experience is preferred.
  • Ability to travel up to 10%, international and domestic, is required.

Nice To Haves

  • Good python scripting knowledge.

Responsibilities

  • Design and lead test method and equipment development, production, and qualification projects.
  • Work closely with Systems, R&D, and Quality engineering to ensure equipment meets internal customer needs.
  • Communicate plans to technical and non- technical leadership.
  • Manage technicians and vendors to implement equipment designs and testing.
© 2024 Teal Labs, Inc
Privacy PolicyTerms of Service