Location: Germany (Hybrid)
Contract: 12 months
About the Role
We are looking for an experienced Systems Engineer to join a leading medical device manufacturer in Germany. This is a hybrid role supporting the development and compliance of Class IIb/III medical devices.
Responsibilities
* Manage system requirements and design controls in line with ISO 13485 and EU MDR.
* Support verification and validation activities for hardware/software systems.
* Conduct risk management (ISO 14971) and ensure regulatory compliance.
* Collaborate with cross-functional teams on design, quality, and manufacturing transfer.
Requirements
* Degree in Engineering or related field.
* 5+ years' experience in medical device development (Class IIb/III).
* Strong knowledge of ISO 13485, IEC 60601, IEC 62304, and EU MDR.
* Fluent English; German is a plus.
Details
* Duration: 12 months
* Start: ASAP
* Working Model: Hybrid (Germany-based)