- Maintenance of serial product documentation (DHF, DMR)
- Optimization of serial products and components
- Qualification, validation and verification of products and components
- Support complaint processing through root cause analyses Initiation, planning, coordination and implementation of product changes
- Project management of international life cycle projects
- Processing of customer inquiries incl. calculation
Requirements
- Successfully completed engineering studies in the field of medical technology, mechanical engineering, plastic technology or similar
- At least 3 years of professional experience in the field of medical device development, especially of injection molded parts
- Knowledge of relevant quality standards and technical norms
- Professional experience in qualification, validation and verification of medical devices
- Good knowledge of common MS Office products and 3D CAD systems
- Business fluent English language skills, written and spoken
- High ability for Teamwork Goal-oriented and structured way of working, hands-on mentality
medmix
medmix is a global leader in high-precision delivery devices, occupying leading positions in healthcare, consumer, and industrial end-markets
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