Location
Siziano
Job Type
Temps plein, Permanent
Posted
July 14, 2026
Job Description
DESCRIPTION DU POSTE
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...
The resource will be included in a very technical and professional pharmaceutical quality team.
The new joiner will also actively participate in the review of the processes, pushing towards the innovation of the entire quality process.
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