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. 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 (DQ, IQ, OQ) and risk assessments. Verify correct management of storage and transport conditions, including temperature‐controlled environments.
What we would like you to bring Degree in a scientific discipline (Pharmacy, CTF, Biology, Chemistry, or related fields). Minimum 2 years of experience in Quality Assurance within the pharmaceutical industry (manufacturing and/or logistics). Eligibility or qualification as a Qualified Person (QP) considered a strong plus. Solid knowledge of Quality Management Systems (paper‐based and e QMS). Proficiency in Microsoft Office and familiarity with WMS/ERP systems. Experience managing audits and regulatory inspections. Strong analytical mindset, accuracy, and attention to detail. Effective communication skills and ability to collaborate across teams. Ability to work independently, managing priorities and deadlines. Good command of English and a proactive, problem‐solving attitude. What's in it for you By joining the Kuehne+Nagel team, you'll have the opportunity to work in a safe and stable environment, with a strong focus on physical and
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