Lead Software Engineer (m/f/d)
Novanta Europe GmbH
Berlin · Onsite · Full Time
Posted
Job description
This position is part of Novanta’s Advanced Surgery business unit. Specialized in the field of Minimally Invasive Medicine, Novanta Medical develops devices and accessories so that doctors can operate with small cuts. We produce Cameras, Insufflators, Medical Pumps, and tubing that makes diagnosis and treatment easier for everyone. Our insufflators and pump systems dilate cavities in the body and turn previously complicated surgeries into minor procedures. Together with customers, doctors, and technical experts, our teams continuously search for new ways to innovate. Tasks Primary Responsibilities Leading software development for medical devices and guiding engineers in the implementation of software solutions Leading the transformation from classical software development to AI-supported software development within the team Requirements analysis based on the functional specification or other requirements Creating and reviewing software requirements and maintaining the required software and device documentation for medical-device development, including documentation needed for compliance, traceability, and product lifecycle support Conducting design and code reviews Independent planning of tasks for oneself and the team Creation and execution of software tests Analysis and correction of software modules in highly complex error cases Applying software standards and ensuring standards within the team Creating and maintaining comprehensive technical and regulatory documentation to ensure compliance with FDA and ISO 13485/IEC 62304 standards Further development of internal software standards Assumption of advanced technical or organizational roles within the organization (e.g., Product Owner) Leading and organizing training sessions on software development practice, tools, and standards Support for strategic decisions in the specialist area through preparation, evaluation, recommendation, and advice Additional Responsibilities Leading software development for regulated medical devices and supporting engineers in complex implementation decisions Identifying, evaluating, and introducing AI-supported software development practices, tools, and workflows in the specialist area Supervision of students and external development service providers with focus on technical quality, regulatory expectations, and team learning Assessment of the impact of changes to standards,…