Systems Engineer

at  Neoventa Medical AB

Neoventa Medical is a Swedish medical technology company founded in 1997. Neoventa provides innovative solutions and services for fetal monitoring that enhance maternity care. Our solutions are designed to promote patient safety through improved decision support combined with a structured workflow. Every day, healthcare professionals around the world use our unique solutions to ensure a good start in life.
Our product portfolio offers a complete solution for monitoring mothers and fetus during labor. In addition to our CTG device, the STAN S41, we are the only company to offer ST analysis of the fetal ECG – a vital complement in assessing the fetus’s condition during delivery. We are also the supplier of internal fetal monitoring electrodes under the Goldtrace brand. Another important area of our business is our comprehensive training program, the Neoventa Academy, where we organize courses in CTG interpretation and ST analysis.
We are currently in an exciting growth phase and are looking for a passionate and experienced Systems Engineer to help shape our future at our headquarters in Mölndal. As a leading player in medical technology for maternity care, we strive for innovation and sustainable development, and we need a key team member to strengthen our R&D team. The team includes two software engineers, a technical product manager, a project manager, and you will report to the R&D Manager.

SYSTEMS ENGINEER

Are you ready to lead the development of advanced hardware solutions in the field of fetal monitoring? We’re seeking a skilled and motivated engineer to take on the role as Systems Engineer for our CTG (Cardiotocography) monitoring systems. This position is key to driving our mission to improve healthcare outcomes through high-quality, reliable technology in clinical settings.

QUALIFICATIONS

• Bachelor’s or Master’s degree in Electrical Engineering, Biomedical Engineering or a related field.
• Proven experience in hardware development, within a regulated environment.
• Expertise in requirement gathering, documentation, and verification processes.

PREFERRED SKILLS

• Knowledge of cardiotocography or fetal monitoring systems.
• Worked actively with quality management systems and design control processes.
• Understanding of medical device standards and regulatory requirements (e.g., IEC 60601, ISO 13485).
• Experience working with international partners, particularly in China.

SOFT SKILLS

• Strong decision-making abilities and a proactive approach to problem-solving.
• Ability to take initiative and drive projects forward, balancing both technical and strategic goals.
• Good communication and technical documentation abilities, especially in a collaborative, cross-cultural environment.
• Ability to see the bigger picture and make decisions that drive value for both our clients and the company-

• Lead hardware development and integration for CTG monitoring systems, taking ownership of key technical decisions and initiatives.
• Define, document, and manage hardware requirements and specifications, proactively identifying areas for enhancement and improvement.
• Work in a cross-functional team and coordinate with Chinese partners to ensure alignment on technical standards and product goals.
• Conduct risk assessments and performance testing to ensure product reliability and effectiveness in clinical settings.
• Troubleshoot hardware issues, propose solutions, and lead efforts for continuous improvement and optimization.