PCI Pharma Services in León, Spain is seeking an Administrative Documentation Specialist for the R&D; team.
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You will manage document control, GMP compliance, and data integrity across trials and manufacturing processes.
The role requires coordinating with QA, QC, Supply Chain, and project teams, plus proficiency with Smartsheet and Microsoft Office.
Strong organizational skills and meticulous attention to detail are essential. xqbhyrx
Experience with cGMP documentation practices is highly desirable.