**The resource will be included in a very technical and professional pharmaceutical quality team.**

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The new joiner will also actively participate in the review of the processes, pushing towards the innovation of the entire quality process.

**How you create impact**

+ Ensure compliance with GDP/GMP and applicable national and international regulations across all logistics activities.
+ Maintain and continuously improve the Quality Management System (QMS).
+ Draft, review, and approve SOPs, operational instructions, and quality documentation.
+ Manage deviations, non‑conformities, CAPA, and change control processes.
+ Oversee complaints, returns, and product recall activities.
+ Conduct and support supplier qualification, including internal and external audits.
+ Prepare for and support customer and regulatory inspections.
+ Deliver training programs and ensure proper staff qualification.
+ Review validation documentation...