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(Advanced / Senior) Project Engineer for Systems Engineering (m/w/x)
Systems engineering for neuromonitoring and neurostimulation devices. Master's degree and several years of medical device development experience required. 30 vacation days, Christmas and New Year's Eve off.
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Anforderungen
- Master’s degree in Physics, Medical Engineering, Electrical Engineering, Mechanical Engineering, or related technical/scientific discipline
- Several years of medical device development, systems engineering, or R&D experience
- Proven track record leading complex medical device development projects
- Strong expertise in requirements engineering, design control, verification & validation, and risk management
- Sound understanding of medical device regulations and standards (MDR, FDA)
- Strong analytical, technical, and problem-solving skills
- Ability to work effectively in multidisciplinary teams
- Excellent communication skills
- Excellent stakeholder management skills
- Excellent project leadership capabilities
- Fluent English
- Advantageous German language skills
- Experience with FDA submissions
- Experience with clinical evaluation
- Experience with usability engineering
- Experience with human factors engineering
- Experience with electrical or electromechanical systems
- Technical leadership experience within cross-functional development teams
- Passion for innovative medical technologies
- Strong interest in Intraoperative Neuromonitoring (IONM)
- Strong interest in Neurosurgery and Spine Surgery
- Strong interest in Thyroid and ENT Surgery
- Strong interest in Neurophysiological monitoring
- Strong interest in signal acquisition and measurement systems
Aufgaben
- Lead systems engineering activities through the product lifecycle.
- Define, analyze, and maintain system requirements with end-to-end traceability.
- Drive cross-functional collaboration with engineering, quality, regulatory, clinical, and manufacturing teams.
- Evaluate technical concepts, architectures, and designs for performance, reliability, and safety.
- Coordinate risk management, design reviews, verification and validation, and technical assessments.
- Support regulatory submissions and compliance with MDR, FDA, and other requirements.
- Manage technical risks, drive problem-solving, and ensure project execution for scope, timeline, and quality.
- Serve as a technical expert and mentor in development teams.
Berufserfahrung
Ausbildung
Sprachen
Benefits
- Flexible working hours
- Mutually-supportive team
- Meaningful work
- 30 vacation days
- Christmas Eve and New Year's Eve off
- Team and company events
- Company fitness program
- Training and continuing education
Von Nejo automatisch aufbereitet
Nejo hat diesen Job automatisch von der Website des Unternehmens Dr. Langer Medical GmbH erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Zur Originalanzeige bei Dr. Langer Medical GmbHÜber das Unternehmen
Das Unternehmen ist seit mehr als 25 Jahren auf die Entwicklung und Vermarktung hochinnovativer Medizintechnik spezialisiert.
Nejo bewertet ihn, und bringt ihn danach gemeinsam mit dir in Bestform.
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