Du koordinierst die Produktentwicklung und arbeitest an der Erstellung der medizinischen Produktdokumentation sowie an Verifikationstests.
Anforderungen
- •Education in Engineering or related discipline
- •Analytical mindset and creativity
- •Experience with technical documentation
- •High documentation quality standards
- •Well-organized working style
- •Fluent written and spoken English
- •German is a plus
- •Experience with sterile goods
- •Experience with medical electrical devices
Deine Aufgaben
- •Koordination interner und externer Produktentwicklungsaktivitäten
- •Anforderungsmanagement mit Produktmanagement und Experten
- •Erstellung der Produktdokumentation für medizinische Geräte
- •Kommunikation mit F&E, Herstellern und internen Teams
- •Definition und Überprüfung technischer Konzepte
- •Aufbau von Prototypen und Qualifizierung von Bauteilen
- •Definition und Durchführung von Verifikationstests
- •Expertenkompetenz innerhalb des Teams besitzen
Deine Vorteile
Internationale Teamunterstützung
Bedeutsame Arbeit mit Einfluss
30 Urlaubstage plus spezielle Tage
Flexible Arbeitszeiten
Regelmäßige Team- und Firmenveranstaltungen
Internes Fitnessprogramm
Umfangreiche Weiterbildungsangebote
TOP 100 Innovator 2022
Original Beschreibung
## Job Description
As a Project Engineer in the R&D Division you will be part of an multidisciplinary and highly skilled team, responsible for development of intraoperative Neuromonitoring and accessories that are used in various clinical use cases.
Your work includes the support of ongoing development projects and you will be responsible for the planning, coordination and execution of technical projects within the company. You work closely with various departments to ensure that projects are completed on schedule and according to technical specifications.
Typical areas of your responsibility are:
* Coordination of internal and external product development activities of intraoperative Neuromonitoring
* Requirements Engineering with colleagues from Product Management, surgeons and technical experts
* Creation of the medical device product documentation (e.g. technical files, risk management and clinical documentation)
* Communication with R&D departments, manufacturers and other internal teams (QM, Manufacturing, Purchasing)
* Definition and review of technical concepts
* Set-up of prototypes and qualification of product components
* Definition and execution of verification tests
* Expert competency ownership within the team
## Qualifications
* Education in Engineering or related discipline, or equivalent working experience
* Analytical mindset and creativity to develop reliable solutions
* Experience with technical documentation for medical devices under MDR and/or FDA
* High documentation quality standards
* Well-organized and clearly structured working style
* Fluent written and spoken English, German is a plus
* Experience with sterile goods or medical electrical devices is a plus
## Additional Information
* A mutually-supportive, international team
* Meaningful work with a lasting impact on medical technology
* 30 vacation days, plus December 24th and December 31st
* Flexible working hours
* Regular team, and company events
* Internal company fitness program
* Comprehensive training and continuing education opportunities offered by Brainlab
* TOP 100 innovator and employer of the future 2022
Contact person: Géraldine Ferrer