Job Summary

As a working student, you will support the engineering team in the preparation, execution, and documentation of qualification and validation activities in a pharmaceutical environment. You will work on project-specific tasks to ensure the GMP-compliant implementation, modification, or optimization of processes and technical equipment.

Your responsibilities include, among other things, the creation, maintenance, and revision of technical documentation (e.g., URS, risk analyses, test plans, reports), participation in the planning and execution of qualification and testing activities, as well as the analysis and preparation of project-related data. You will also support project management through research activities, meeting preparation, minute-taking, and coordination of smaller work packages.

In close collaboration with engineers, Quality Assurance, and production, you will gain in-depth insights into regulatory requirements and the...