Description
This role involves contributing to the definition and structuring of reference frameworks and document management systems within the Quality and Pharmaceutical Affairs Department. The individual will ensure regulatory, quality, and contractual compliance of documentation practices, focusing on traceability, reliability, and adherence to established procedures. Responsibilities include managing the document lifecycle, providing author templates, conducting quality checks, registering documents in the GED, organizing workflows, participating in system improvements, and performing self-assessments.
