Assignment Description:

We are looking for a Senior Embedded Electronics Engineer to join our dynamic team.

What you will work on:

• Design and optimize PCB layouts for the nRF52 platform, with a focus on BLE functionality, signal integrity, analog and digital signal processing, and power management.
• Develop schematic designs and select appropriate components (e.g., ADCs, DACs, BLE antennas, power management ICs) to meet both performance and medical device requirements.
• Oversee the end-to-end PCB manufacturing process, coordinating with vendors, ensuring quality standards, and maintaining production timelines.
• Create and document hardware development stages, including schematics, layout files, and BOM, in compliance with SOPs and regulatory guidelines (ISO 13485).
• Ensure hardware design and documentation comply with medical device standards such as IEC 60601 and ISO 13485 for electrical safety and electromagnetic compatibility.
• Design and implement internal and external verification and validation (V&V) protocols, including EMC testing, to confirm hardware functionality and compliance with performance and safety standards.
• Collaborate with firmware engineers, QA, and regulatory teams to troubleshoot and resolve issues, ensuring alignment across design, testing, and compliance processes.
• Support prototyping efforts, ensuring prototypes are ready for both internal and external testing and feedback.

What you bring:

• Over 5 years of professional experience in embedded electronics development and PCB layout, preferably in the medical device industry.
• Proven experience with the nRF52 series and BLE-enabled hardware design.
• Expertise in Altium Designer for schematic capture, PCB layout, and design rule management, with a strong focus on trace routing, impedance control, and optimization for RF and mixed-signal designs.
• In-depth knowledge of analog and digital circuit design, including signal processing, power regulation, and BLE communication.
• Familiarity with medical device standards such as IEC 60601 for electrical safety and ISO 13485 for quality management.
• Proficiency with testing and debugging tools, including oscilloscopes, multimeters, and spectrum analyzers, to verify analog and digital performance and troubleshoot issues.
• Experience creating regulatory-compliant hardware documentation, including firmware lifecycle documentation in accordance with IEC 62304.
• Experience leading verification and validation (V&V) activities in compliance-driven environments.
• A Bachelor’s or Master’s degree in Electronics Engineering, Biomedical Engineering, or a related field.

Preferred Qualifications:

• Experience with medical devices, particularly electrical stimulators or other therapeutic hardware, and a deep understanding of the medical device development lifecycle.
• Strong attention to detail, analytical skills, and a proven ability to troubleshoot complex design issues, optimizing for safety, functionality, and manufacturability.
• Experience coordinating with PCB manufacturers, managing production timelines, and ensuring quality and compliance at each stage.

If this sounds interesting, please send your CV to cv@veritaz.se