Solution Systems Engineer
Roles:
The Solution System Engineer leads the functional specification and development of platform of radiotherapy solutions, systems, and their decomposition across several product generations and/or platforms, their verification, use, re-use, and timely renewal. The role owns the integration of technical solutions within the R&D Devices Engineering organization with a focus on Linacs engineering solution development in accordance with applicable design control and medical devices directives. A key responsibility for this position is the strategic and operational implementation of the DfX methodology to ensure that non-functional requirements relevant to the business strategy such as reliability, sustainability, serviceability, or cybersecurity are balanced and implemented as necessary within the product development lifecycle and in continuous engineering projects.
Responsibilities:
- Responsible for the overall design of the solution architecture (including HW, SW, IT infrastructure, documentation, and the integration of 3rd party solutions) to the level that it can be realised by project teams.
- Responsible for the safety and Security of the system as design authority and has an accountable sign off for the hazard analysis reviews.
- Accountable for the timely realization of the solution architecture in modular, easy to maintain and extensible systems.
- Responsible for the development of a solution roadmap of all parts allowing decoupling of product lifecycle and features improvements, including scenarios to meet potential future product specifications.
- Accountable for the definition and responsible for the deployment of HW/SW platforms inside the roadmaps.
- Responsible for the architectural aspects of the verification of the requirements to the overall solution.
- Collaborate with the (Domain-) System Engineers, Advanced Development, the Clinical Application Development and Product Management, Procurement on the alignment between the product-, innovation-, technology- and domains roadmaps.
- Excellent understanding and command of requirement engineering including requirements formulation, requirements management and the overall requirements lifecycle.
- Responsible for the translation of stakeholder needs in solution requirements for new product development as wells as continuous engineering projects and programs.
- Develop innovative solutions with suppliers and partners and support strategic supplier relationships.
- Define and accept work elements (epics, features) to realise product roadmaps.
Required Experience:
- First or master's degree in an engineering, physics, or applicable technical/scientific discipline
- Several years of experience in a leading system engineering or systems architecture role, preferably in the medical device industry
- Ability to apply system thinking to product ownership throughout the lifecycle.
- Experienced in the application of system engineering practices taking the value creation for the customers and the company into account.
- Medical sector specific knowledge is preferable, including ISO 13485, IEC 60601, IEC60976 and ISO 14971 and a practical understanding of product development in a regulated industry is key.
- In-depth understanding of all forecasted technological developments of all important and relevant technologies and their application to the sector
- Ability to promote and lead for a strategic, lean and value-optimizing working culture.
- Demonstrated aptitude for strategic thinking and problem solving with the ability to implement through others.
- Excellent communication skills (verbal and written). Ability to speak and present publicly.
- Strong in building and maintaining successful and effective working relationships with other system engineering colleagues.
- Personality based on strong ethical standard, values, and good judgement.
- Good command of systems engineering methods and tools including system modelling
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