Part-Time Controlled Document Specialist | Controlled Document Specialist in Teilzeit | M/W/D - Referenz 001123

Job Summary

This part-time position (50%) involves managing the complete lifecycle of local and global documents within the pharmaceutical industry. Working for an internationally successful pharma company in Oberschwaben, you will coordinate and execute document workflows using the eDMS Vault Quality system. Your day-to-day responsibilities include managing revision processes, ensuring the timely distribution of information across relevant interfaces, and monitoring signature cycles. Beyond administrative tasks, you will serve as a consultant for authors regarding document creation, template usage, and coding. This role is ideal for professionals who value high quality and systematic work. The position offers a hybrid working model, allowing for a mix of remote and on-site work in Biberach, providing a flexible yet collaborative environment within a technologically innovative project setting.