Documentation Specialist

Location: Origgio

Experteer Overview As a member of Manufacturing & Global Operations, you drive quality and continuous improvement across the value chain. You will manage GMP documentation, deviations, CAPA, and data integrity, collaborating with QA, documentation, and production teams. You’ll support product quality analysis and batch record reviews, leveraging analytical tools to sustain high standards.

This role offers hands‑on impact in a global, collaborative environment focused on quality and efficiency. Join us to help advance Grünenthal’s future by strengthening processes and compliance.

Retribuzione / Benefits Manage GMP documentation including Events and Deviations, Root Cause Analysis, and CAPAHandle complaints in collaboration with QA Operations using Master Control, LIMS, MESCollaborate with documentation team and bulk manufacturing supervisors; involve production personnel and training management

Maintain Data Integrity compliance

Update and manage documentation per GMP regulations

Support analysis and review of product quality attributes (OPV; PQR) using Minitab and other statistical tools

Support review and modification of Production Department Master Batch Records (SAP)
ResponsabilitàMaster's degree as listed

English language proficiency (B2/C1)
Detail‑oriented with analytical and time‑management skills

Collaborative mindset and strong team spirit

Requisiti fondamentali

Master's degree as listed

English language proficiency (B2/C1)
Detail‑oriented with analytical and time‑management skills

Collaborative mindset and strong team spirit
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