Support for qualification, validation, and maintenance of equipment and facilities. The role is within the Clinical Supply Quality team, focusing on packaging and labeling for clinical studies. The position is critical for ensuring quality systems and compliance in the production, release, and distribution of Investigational Medicinal Products (IMPs) for clinical trials. - Review of batch records (both electronic and paper). - Review and release of labels. - Release of warehouses and production consumables specification. - System-related activities: deviation review, CAPA (Corrective and Preventive Actions), change control. - Participation in audits, regulatory inspections, and vendor
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