Senior Project Engineer, Systems Engineering

Salary: 70.000 - 100.000 € per year

Requirements:

Masters degree in Physics, Medical Engineering, Electrical Engineering, Mechanical Engineering, or a related technical or scientific discipline.

Several years of experience in medical device development, systems engineering, or R&D.

Proven track record of leading complex medical device development projects across the full product lifecycle.

Strong expertise in requirements engineering, design control, verification and validation, and risk management.

Sound understanding of medical device regulations and standards, including MDR and FDA requirements.

Strong analytical, technical, and problem-solving skills, with the ability to work effectively in multidisciplinary teams.

Excellent communication, stakeholder management, and project leadership capabilities.

Fluent in English; German language skills are an advantage.

Preferred qualifications include experience with FDA submissions, clinical evaluation, usability engineering, human factors engineering, electrical or electromechanical systems, and technical leadership within cross-functional development teams.

Passion for innovative medical technologies and a strong interest in intraoperative neuromonitoring (IONM), neurosurgery and spine surgery, thyroid and ENT surgery, neurophysiological monitoring, signal acquisition, and measurement systems.

Responsibilities:

Lead systems engineering activities throughout the medical device development lifecycle, from concept development to product launch and sustaining engineering.

Define, analyze, and maintain system requirements while ensuring end-to-end traceability through design, verification, and validation.

Drive cross-functional collaboration between engineering, quality, regulatory, clinical, and manufacturing stakeholders.

Evaluate technical concepts, system architectures, and design solutions to ensure product performance, reliability, and patient safety.

Coordinate risk management, design reviews, verification and validation activities, and technical assessments.

Support regulatory submissions and compliance activities in accordance with MDR, FDA, and other applicable regulatory requirements.

Manage technical risks, drive problem-solving activities, and ensure successful project execution with respect to scope, timeline, and quality objectives.

Serve as a technical expert and mentor within interdisciplinary development teams.

Technologies:

Support

Marketing

More:

Dr. Langer Medical GmbH, based in Waldkirch, Germany, has been part of Brainlab SE in Munich since 2022. For more than 25 years, we have specialized in developing and marketing innovative medical technology for intraoperative neuromonitoring and neurostimulation. Our products are distinguished by their design and handling and support our worldwide growth; both our products and our company have received several awards. We offer a mutually supportive, international team, meaningful work with a lasting impact on medical technology, 30 vacation days plus December 24 and 31, flexible working hours, regular team and company events, an internal fitness program, and comprehensive training and continuing education opportunities through Brainlab. We were recognized as a TOP 100 innovator and employer of the future in 2022. We look forward to receiving your online application, including your earliest available start date and desired salary.

last updated 43 week of 2026