Tech Lead (Embedded Systems)
About the Role
Looking for your next challenge in Embedded Systems Engineering?
Passionate about driving innovation in cardiovascular healthcare?
Join our client in Berlin and be a key part of their mission to make a real impact!
Key Responsibilities:
Oversee the design, development, and refinement of embedded systems for medical devices, ensuring top-tier reliability, safety, and efficiency
• Create and manage embedded firmware and software, including low-level device drivers, real-time operating systems, and communication protocols
• Conduct system analysis and debugging to diagnose and resolve intricate issues in embedded systems
• Assist in the preparation and review of technical documents such as design specifications, test plans, and user guides
• Ensure adherence to medical device regulations, including FDA, ISO, and other industry standards
• Perform code reviews and provide technical guidance to junior engineers
• Collaborate with cross-functional teams to outline system requirements and ensure they align with project goals
• Ensure successful system development and delivery by balancing technical needs, resources, and stakeholder expectations throughout the project’s life cycle
• Recruit and manage a team of developers, including both freelancers and full-time employees
• Stay informed about emerging technologies and industry trends to enhance existing systems and explore new opportunities
Requirements:
- A degree in Electronics, Electrical Engineering, or a related field.
- 7+ years of experience in embedded systems engineering, with significant exposure to medical device development (or another regulated industry)
- Skilled in embedded C/C++ programming with hands-on experience in real-time operating systems (RTOS) and Linux
- Strong knowledge of hardware-software integration, including working with microcontrollers, sensors, and communication interfaces
- Experience with version control tools (e.g., Git) and development environments, including IDEs, debuggers, and CI/CD automation
- Excellent communication and teamwork skills, capable of working in a multidisciplinary environment
- Knowledgeable about medical device regulations and standards, such as IEC 62304 and ISO 13485
- Experience with safety-critical systems and software development life cycle (SDLC) methodologies is essential
If you're interested in this position, please apply and/or contact Hollie Dear at Adaptive Life Science for more information.