Experteer OverviewIn this role you will support QA and regulatory activities within DHL's Life Sciences & Healthcare operations in Rome. You help implement and maintain quality policies, conduct audits, manage documentation, and drive continuous improvement to ensure GxP compliance. You will work on regulatory tasks, ensuring proper storage and distribution compliance and supporting CAPA and training programs. This position offers impact by safeguarding quality standards in a pharmaceutical warehouse setting, contributing to reliable service for customers and patients. You will collaborate with cross‐functional teams to sustain high standards and adapt to changing regulatory requirements.Benefits and ResponsibilitiesSupport the preparation, implementation, and maintenance of Quality Assurance policies and procedures.Assist in conducting internal and external auditing activities.Maintain archive of quality documentation and update relevant reports/KPIs.Ensure adherence to GxP standards and quality requirements.Help ensure storage and distribution laws/regulations for human, narcotics and veterinary medicines are followed.Support managing pharmaceuticals in compliance with existing SOPs.Assist in monitoring temperatures and trend deviations across environments and assess paths for compliance.Collaborate on narcotics management: purchase orders, periodic reporting, import/export permits, and documentation.Contribute to root cause analysis and define CAPA using DHL's tool.Develop projects in the Pharma BU for involved sites.Support management of training and annual training programs in Quality/GDP, GMP area.ResponsibilitiesDegree in Pharmacy, Chemistry, Pharmaceutical Chemistry and Technology (CTF), or related fields.Good understanding of regulatory requirements, QA tools, and methodologies.Proficiency in English.Proficiency in Microsoft Excel and PowerPoint.Previous experience in the pharmaceutical sector and/or supply chain operations is preferred.
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