The Documentation Management Expert (QMS Transformation) plays a key role in a cross‑functional program aimed at the end‑to‑end transformation of the Quality Management System (QMS). The role is responsible for designing the future‑state QMS documentation architecture, including document hierarchy, metadata model, lifecycle processes (including translation), and governance, ensuring alignment with GxP regulations, industry standards, and internal quality strategy. Key Responsibilities * Experience with document control processes and QMS frameworks in the pharmaceutical or biotech industry. * 3–7 years of experience in documentation management, quality systems, or related quality roles in the pharmaceutical industry.
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