Drive and support design control and product risk management activities in development projects.
Translate stakeholders into clear, high-quality system and subsystem requirements with end-to-end traceability.
Own and contribute to systems engineering documentation, including design input/output, product description, and risk documentation.
Support design verification and validation planning and execution in close collaboration with Test Engineering.
Participate in design reviews, change control, and impact assessments.
Ensure compliance with applicable regulatory and quality requirements (e.g. MDR, FDA, ISO 13485, ISO 14971).
Collaborate closely with cross-functional project teams to support timely project execution.
Requirements
Degree in engineering or a similar technical discipline.
Experience with systems engineering and design control in a regulated environment (medical devices are an advantage).
Knowledge of risk management, requirements engineering, and traceability.
Experience working cross-functionally with R&D, Test, Quality, and Regulatory stakeholders.
Strong analytical and communication skills.
Experience with Polarion or similar ALM tools is an advantage.
Benefits
A 12-months temporary position in a collaborative and learning environment with strong focus on quality, high professional standards, good sparring and learning.
You will get real responsibility from the start and the opportunity to build strong capability in systems engineering and regulated product development.
You will collaborate closely with experienced colleagues in Systems Engineering, Test Engineering, and Product Development.