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Arbetsbeskrivning
Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in securing the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry.
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.