Job Responsibilities Implement systems engineering approach to support the development and life cycle management of complex products and platforms in the areas of connected drug delivery devices. Contribute to the development of complex medical devices using state-of-the-art system engineering practices. This highly interactive role will work with cross-functional teams and support various development activities including requirement elicitation, system conceptualization, risk assessment, system verification, and validation. Guarantee a holistic approach to the development considering and balancing all aspects that concur to the success of the product: purpose, business needs, constraints, technical challenges, feasibility, and trade-offs. Guide the integration of software-controlled electro-mechanical systems starting from technology exploration, product definition, and development, based on user needs and technical design input requirements. Utilize the system engineering tool for requirements management and translate user and business needs into system/sub-system requirements. Participate in system design/review meetings to ensure appropriate integration and connectivity within the overall system. Define and maintain design history files, the traceability from the requirements to the verification activities and related deliverables. Represent the system engineering team for communications with cross-divisional teams, programs, and stakeholders within multi-cultural and international projects. Collaborate with peers to identify opportunities for process improvement in a fast-paced and growing organization. Maintain up-to-date knowledge of medical devices, technologies, and regulatory landscape related to the company’s products. Support an experienced group of system engineers to develop your skills as a systems engineer. Minimum Requirements Bachelor or more advanced degrees in Systems Engineering, Electrical/Electronic Engineering, Computer Science, Biomedical Engineering, or other relevant disciplines. Relevant industry experience in a highly regulated environment is an advantage. Prior experience covering the medical device product development from concept to commercial launch, working with the requirements and traceability management tools is an advantage. Strong analytical skills and ability to apply engineering principles using logical or scientific thinking to define and solve problems, collect data, establish facts, and draw valid conclusions. Ability to cope with the complexity of inter-disciplinary development team coordination. Ability to capture and decompose customer needs into device and sub-systems requirements and engineering specifications. Document design input & output. Experience in systems design with good abstraction skills, system modeling, analyze problems and synthesize solutions. Provide solid technical skill and engineering support for design, development, and troubleshooting activities. Strong interpersonal and communication skills and ability to effectively work in a diverse, team-driven environment. Proficient use of Office applications like MS Outlook, Excel, Word, PowerPoint, Visio, and Project. Strong English written and verbal communication skills with both technical and non-technical users. Knowledge of German is an advantage. Equal Rights Wir verpflichten uns zu einem integrativen Einstellungsverfahren und zur Chancengleichheit für alle unsere Bewerber. Alle Bewerber werden unabhängig von ethnischer und nationaler Herkunft, Hautfarbe, Glaube, Religion, Alter, Geschlecht, Geschlechtsidentität, sexuelle Orientierung, Familienstand, Behinderung, genetische Informationen, Staatsbürgerschaft oder einen anderen gesetzlich geschützten Status berücksichtigt. Menschen mit Schwerbehinderung werden bevorzugt eingestellt. #J-18808-Ljbffr