A permanent contract with the leader in innovation and high-tech engineering consulting
A multi-stage model with career opportunities through specialization prospects, as well as with over 45'000 consultants around the world and revenue of EUR. 2.9 Bn, the Altran Group is the undisputed global leader in Engineering and R&D services (ER&D).
In Switzerland, Altran employs more than 250 consultants and aims towards large growth with offices located in Zürich, Basel, Lausanne and Geneva.
• Design and implement system engineering approach to support the development and life cycle management of complex products and platforms in the areas of connected drug delivery devices, digital technologies, and SaMD
• Demonstrate strong technical know-how at system level and guide the development team to use structured system engineering approach for product development
• Utilize the system engineering tool for requirement management and translate user and business needs into system/sub-system requirements
• Actively maintain and monitor the traceability from the requirements to the verification activities
• Be the representative of system engineering for the communications with cross-divisional teams, programs, and stakeholders
• Manage external vendors for development and lead the technical discussions with the vendors
• Author relevant design history files and GMP compliant documentations
• Bachelor or more advanced degrees in Biomedical Engineering, Systems Engineering, Electronic Engineering, Computer Science, or other relevant disciplines
• Track record of going through the product development cycle, from prototype to commercial launch, in the medical device industry or GMP environment is highly valued
• Good knowledge in systems engineering approach and risk-based approach for product development
• Experience working with the requirements and traceability management tools
• Knowledge in system functional modeling and/or programming ability using system modeling language (SysML) will be a plus
• Experience in developing and commercializing products using artificial intelligence or machine learning models is a strong advantage
• Well-versed in medical product development, Quality Management System, and regulatory processes (ISO 13485; IEC 60601, 62304, 82304)
• A good team player, and problem solver with strong analytical mind
• Strong communication skills to both lead the technical discussions with vendors and also align with internal stakeholders to drive decisions
Please note, that we only accept applicants with Swiss or EU/EFTA citizenship or applicants with an existing and valid residence and work permit for Switzerland.