Robotics & Digital Solutions, part of our customer Johnson & Johnson family of companies, we are recruiting a Technical Writer, located in Norderstedt or Munich, Germany.Your employment begins as a temporary employee, a transfer by JnJ into a direct employment relationship is planned.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.Our customers software engineering team in Germany needs a Technical Writer. The engineering team needs to deliver documentation for the Software as Medical Device (SaMD), including software development plans, software architecture documents, software detailed description, SOUP assessment, testing reports, release notes, and other engineering/technical documents required for regulatory submission. All documentation is written in English, needs to be discussed in English, and then routed for approvals through our systems. We expect the technical writer to be native English speaker, bilingual, or at least proficient in technical conversation. Residence in Germany.As a Technical Writer you will be a key member of a team delivering cutting edge Digital Surgery software. The software is considered a medical device, and supports surgeons pre- and intra-operative. Therefore, the documentation follows the standards for medical device manufacturing. Your direct responsibility will be to support engineering teams in writing technical documentation, discussing the content with cross-functional stakeholders, and managing the approval and document release process.