Scientist / Device Engineer | Scientist / Device Engineer | M/W/D - Referenz 001130

Job Summary

This role involves joining an internationally successful pharmaceutical company in the Mainz area to lead the design verification of medical devices and combination products. You will be responsible for planning, executing, and coordinating design verification studies while ensuring strict compliance with regulatory requirements. Your day-to-day will involve representing the evaluation engineering department within the device development team, managing work packages for design verification, and creating submission-relevant plans and reports. You will also collaborate closely with cross-functional teams including Design Engineering, Quality, Risk Management, and Usability Engineering. This position is particularly attractive for professionals seeking a hybrid work model within a highly regulated, innovative environment. It offers the chance to influence the development cycle of life-saving medical products and contribute to the evolution of regulatory standards within a leading global organization.