Systems Engineer Medical Devices at Novanta Europe GmbH

Berlin, , Germany -

Full Time

Start Date

Immediate

Expiry Date

11 Feb, 26

Salary

0.0

Posted On

13 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Systems Development, Software Design, Embedded Systems, Hardware, Software, Mechanics, Requirement Management, Communication Skills, Team Player, Design To Cost, Verification Procedures, Product Transfer, ISO 13485, Technical Documentation, Risk Management, Agile Methodology, Cyber Security

Industry

Medical Equipment Manufacturing

Description

Please check out the Novanta career site for detailed job description: https://novanta.wd5.myworkdayjobs.com/en-US/Novanta-Careers?q=R008545 This position is part of Novanta’s Advanced Surgery business unit. Specialized in the field of Minimally Invasive Medicine, WOM 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. Summary Responsible for the technical realization of products based on defined architecture and master specifications in accordance with company-wide design guidelines Tasks Primary Responsibilities Definition and documentation of the system design based on the specified architecture and platform development, taking into account regulatory and normative provisions Analysis of external/internal stakeholder requirements Pre-selection and allocation of customer requirements to existing solutions of the platform, if necessary coordination with stakeholders Determination of the features to be integrated, if necessary creation of a feature request Responsibility for the technical implementation of new product features, preferably as a reusable component of the platform Creating product-specific system specifications Coordination of technical solutions between the individual departments Technical management of the technical project components and content-related support of the associated work packages (target definition, DoD) together with the project manager and the specialist departments Creation and maintenance of technical documentation together with the project manager Responsible for product-specific risk management in cooperation with the risk manager Responsible for the product-specific verification plans and their successful implementation Technical management of equipment and hose set construction (Alpha, Beta, Vali) Transfer (design transfer) of products into production Responsible for the review and approval of assembly instructions Responsible for standard testing of the device and hose sets Support of manufacturing processes up to the pilot series (NPI); Technical support of production (PE) Control of material and parts list creation/management Creation and maintenance of technical documentation together with the project manager Responsible for the technical release of the products by the customer Technical contact person for customers (e.g. project acquisition), suppliers, external development partners and internal departments Requirements Required Experience, Education, Skills, Training and Competencies Dipl.-Ing./Master Electrical Engineering/ Medical Engineering/ Mechanical Engineering or Materials Engineering/ Biology or equivalent (MSc preferred) Several years of product development experience in the role of systems engineer for Medical Devices Good knowledge of systems development and/or software design Good knowledge of embedded systems, hardware, software and mechanics Experience in defining requirements or requirement management systems Great communication skills Collaborative mindset and a team player, experience in working with an international environment Experience in design to cost Knowledge of verification procedures Experience in transferring products into production Knowledge of relevant norms and standards (e.g. ISO 13485) Professional Working Proficiency in English (C1) Quality-conscious, trustworthy and reliable Willingness to travel to all locations and business contacts Structured, systematic and solution-orientated way of working Preferred qualifications knowledge of Polarion and SAP software knowledge of agile methodology and MS Azure tool Knowledge of cyber security measures and standards Travel Requirements Yes up to 10-20%

Responsibilities

Responsible for the technical realization of products based on defined architecture and master specifications. This includes defining system design, coordinating technical solutions, and managing product-specific risk and verification plans.