Controlled Document Specialist (Part-Time 50%) | Controlled Document Specialist in Teilzeit 50% (m/w/d)

Job Summary

This part-time position involves managing the end-to-end lifecycle of local and global documentation within a pharmaceutical environment. Based in Biberach, you will be responsible for coordinating document revisions, overseeing the signature workflow in the eDMS Vault Quality system, and ensuring the timely distribution of critical information to relevant stakeholders. A key part of the role is acting as an internal consultant for document authors, providing guidance on templates, coding, and procedural workflows. This role is ideal for a detail-oriented professional who excels at maintaining high quality and meeting strict deadlines. Working for a renowned pharmaceutical company through Randstad Professional, you will benefit from a structured corporate environment, attractive compensation, and the stability of a long-term contract. The position offers a unique opportunity to specialize in quality-driven data management while maintaining a balanced 50% part-time schedule.