- Manage and coordinate the transfer of drug delivery devices from Development to Manufacturing
- Prepare and maintain process documentation including process specifications, Process Map, P-FMEA, Product Concept, Manufacturing Concept etc.
- Conception of prototypes and define critical process parameters
- Communication with production site and scheduling of project specific tasks
- Identification of optimization potential in existing production processes
- Collaboration in the definition of processes at external suppliers
- Provide technical support during Root Cause Analysis, and implementation of corrective actions
- Create qualification plans and execute qualification
Must Have:
- Completed studies in a technical field (e.g. mechanical engineering, biomedical engineering, Mechatronics, medical technology)
- Several years of work experience in process development or design transfer of medical devices
- CAD skills (SolidWorks) to design tooling, fixtures, and process-related components
- Good understanding of design-for-manufacturing and design-for-assembly (DFM/DFA) principles
- Experience writing technical documentation and reports of medical devices
- Proficient in English, German skills are desirable
- Being available for occasional travel to our suppliers or our production facility in Czech Republic
Nice To Have:
- Experience with qualification activities (IQ, OQ, PQ) and related documentation
- experience or knowledge in 3D printing technologies (FDM and SLA) for rapid prototyping and process development support
At medmix, you will become part of a renowned team. Attractive compensation and a wide range of additional benefits come as standard. You can expect the following:
- Flexible working hours under our flextime model
- 30 days of vacation per year
- Company pension scheme
- Public transport ticket subsidy
- Pluxee benefit: prepaid card with monthly credit
- Discounts via the "Corporate Benefits" and "Benefits me" apps
- Regular company events