Systems Engineer Disposables (f/m/d) job opportunity at Novanta.

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DatePosted 30+ Days Ago bot
Novanta Systems Engineer Disposables (f/m/d)
Experience: 3-years
Pattern: full-time
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degreeAssociate
loacation Berlin, Germany, Germany
loacation Berlin, German..........Germany

Build a career powered by innovations that matter!  At Novanta, our innovations power technology products that are transforming healthcare and advanced manufacturing—improving productivity, enhancing people’s lives and redefining what’s possible.  We create for our global customers engineered components and sub-systems that deliver extreme precision and performance for a range of mission-critical applications—from minimally invasive surgery to robotics to 3D metal printing. Novanta is one global team with over 26 offices located in The Americas, Europe and Asia-Pacific.  Looking for a great place to work?  You have found it with a culture that embraces teamwork, collaboration and empowerment.  Come explore Novanta. This position is part of Novanta’s Advanced Surgery business unit group. Novanta offers highly reliable, precise and safe solutions that enhance system performance and improve patient outcomes. Insufflators, pumps and disposable tube sets, along with medical visualization and operating room integration technologies are the preferred solution for minimally invasive surgery applications. We are looking for an  Systems Engineer  for our  Disposables Team Summary This job is responsible for the technical implementation of products based on defined architecture and master specifications in accordance with company-wide design control guidelines. The development focus of this position is on medical accessories, e.g. tube sets for insufflators and pumps. Primary Responsibilities Definition and documentation of the system design on the basis of the given architecture and platform development, taking into account regulatory and normative provisions. Analysis of external/internal stakeholder requirements. Pre-selection and assignment of customer requirements to existing solutions of the platform, coordination with stakeholders if necessary. Determination of the features to be integrated, creation of a feature request if necessary. Responsibility for the technical implementation of new product features, preferably as a reusable component of the platform. Creation of product-specific system specifications. Coordination of technical solutions between the individual departments Technical management of the technical project components and content support of the associated work packages (target definition, DoD) together with the project manager and the departments. Preparation 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 the equipment and hose set constructions (Alpha, Beta, Vali). Transfer (design transfer) of the products to production. Responsible for the review and approval of assembly instructions. Responsible for the standard tests of the device and tube sets. Support of manufacturing processes up to pilot series (NPI); Technical support of production (PE). Control of material and BOM creation/management. Preparation and maintenance of technical documentation together with the project manager. Responsible for the technical approval of the products by the customer. Technical contact person for customers (e.g. project acquisition General Tasks Strict compliance with the quality, occupational safety, and environmental regulations. Implementation of the instructions of the quality / environmental management representative and the occupational safety specialist.   Required Experience, Education, Skills, Training and Competencies Training/Education: Dipl.-Ing./Master of Medical Technology / Mechanical Engineering / Materials Engineering / Biology or equivalent Technical Requirements Profile: 3+ years of relevant work experience required. Preferably in the development of medical device disposable products. Good knowledge in the fields of mechanics, sterility, biocompatibility. Experience in Design to Cost. Good knowledge of manufacturing processes of sterile tubing sets (gluing, welding, packaging, etc.). Experience in defining requirements or requirement management systems. Knowledge of verification procedures. Experience in transferring products to production. Knowledge of the relevant standards. Good knowledge of English (CEFR-B2)* Knowledge of SAP desirable Travel Requirements    Willingness to travel to all locations and business contacts (10-15 %)   Physical Requirements Quality-conscious, trustworthy, and reliable Willingness to travel to all locations and business contacts. Able to work in a team. Very good communication skills. Structured, systematic and solution-oriented way of working. #LI-UK1 #Berlin Novanta is proud to be an equal employment opportunity and affirmative action workplace. We consider all qualified applicants without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, military and veteran status, disability, genetics, or any other category protected by federal law or Novanta policy. Please call +1 781-266-5700 if you need a disability accommodation for any part of the employment process.

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