Sr Systems Verification Engineers

Kelly Engineering Outsourcing & Consulting Group (KellyOCG), a managed solution provider and business unit of Kelly Services, is currently seeking Sr Systems Verification Engineers for a long-term engagement at one of our Global Medical Device Robotics & Digital Solutions clients in Santa Clara, CA. A global leader in surgery with products and solutions found in almost every operating room around the world.This role is a full-time, fully benefited position. As a KellyOCG employee you will be eligible for 50% paid Medical & Dental, 401K and a variety of other benefits to choose from. You will also be eligible for paid time off, including holiday, vacation and sick/personal time. All KellyOCG employees receive annual performance reviews.Robotics & Digital Solutions company , is recruiting a Sr . System Verification Engineer , located in Santa Clara, CA.Robotics & Digital Solutions company is a global leader in surgery with products and solutions found in almost every operating room around the world. They have 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.The Sr Systems Verification Engineer will develop and execute system tests, prototype and integrate test equipment, and document test protocols, fixtures, and reports for the Surgical Robotics system. The engineer will manage and own projects, as well as support other engineers in test and equipment development activities. 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.Key Responsibilities:

Design and develop test protocols, support other engineers in test development.

Design, prototype, qualify, and document test fixtures, equipment, and systems.

Develop software test scripts ( primarily in Python ).

Work closely with Systems Integration, R&D, and Quality engineering to ensure tests and equipment meets internal customer needs. Communicate plans to technical and non-technical leadership.

Manage technicians and vendors to support test protocol and equipment goals.

Qualifications:

B.S. in Engineering or other applicable technical degree required

5 years of experience developing and executing test method validation and equipment qualification .

Ability to develop testing protocols and analysis software scripts in Python, MATLAB, and or other scripting languages is required .

Breadth of knowledge across engineering fields (electrical, mechanical, software), with domain expertise in at least one area.

Ability to prioritize tasks from different engineers/managers, demonstrate good time management skills, and communicate.

Test equipment design, prototyping, qualification and implementation.

Medical device or similar regulated industry (e.g. automotive, aerospace) experience.

Proficiency in technical writing and good documentation practice.

Robotics or electro-mechanical experience is preferred.

Ability to travel up to 10%, international and domestic.

Important information: This position is recruited for by a remote Kelly office, not your local Kelly branch. Applicants must be legally permitted to work in the United States immediately and without employer sponsorship.