Participation in development projects from the preliminary phase through verification to production transfer
Analysis and evaluation of customer requirements, product concepts, and specifications
Development and coordination of system requirements, system architectures, and technical interfaces
Close collaboration with project management and other development teams
Linking requirements to risks, technical measures, and verification evidence
Evaluating technical changes and providing support for system integration, verification, and technical reviews
Contributing to the further development of methods, processes, and tools in systems development
Your profile
A successfully completed technical degree in medical technology, electrical engineering, mechatronics, mechanical engineering, computer engineering, or a comparable field
Several years of experience in technical product development, ideally in the field of medical devices or other regulated products
Preferably experience in requirements engineering, system architectures, risk analysis, system integration, or verification
Thorough understanding of regulated development processes, e.g., FDA, MDR, design control
Strong communication and facilitation skills, as well as very good written and spoken German and good written and spoken English
We offer:
Flexible working time models for a work-(family)-life balance
Permanent employment contract
Individual (further) development opportunities
Short decision-making processes
A culture of informality
Team events, summer parties and Christmas parties
Anniversary benefits
Flu vaccinations
And of course the classic fruit basket
Convinced? Then become part of the BYTEC team
Please send your application documents (cover letter, CV, certificates, earliest start date and salary expectations) to Ms. Dipl.-Kff. Claudia Coenen:
