MSAT Packaging ExpertVerviers, Belgium – Full-time, Permanent PositionCompany DescriptionA global leader in pharmaceutical production, committed to delivering cutting-edge solutions that improve health and well-being. At our Verviers site in Belgium, we combine scientific expertise with state-of-the-art facilities to support pharmaceutical manufacturing at the highest level of quality and compliance.DepartmentThe Manufacturing Science and Technology (MSAT) team in Verviers plays a pivotal role in supporting GMP manufacturing operations with technical expertise and project leadership. The group works cross-functionally with production, quality, and analytical teams to optimize manufacturing processes and ensure robust, validated systems.Job DescriptionAs MSAT Packaging Expert, you will serve as the Subject Matter Expert (SME) for packaging, closure integrity, and shipping validation processes. You will lead critical validation projects, contribute to the introduction of new primary packaging materials, and provide scientific and technical support to ensure compliance with EU GMP, ISO13485, and FDA regulations (21 CFR 820).This is a high-impact role where you will collaborate across departments and influence global packaging strategies, ensuring product integrity and patient safety throughout the supply chain.Key ResponsibilitiesLead closure integrity and shipping validation projects in accordance with regulatory and internal standardsEnsure that packaging processes remain in a validated state of controlConduct product quality impact assessments for new primary packaging introductionsExecute and document validation activities, ensuring scientific rigor and compliance with GMP and ISO standardsSupport technical investigations and lead root cause analysis for packaging-related issuesContribute to wider MSAT initiatives and provide expert input into cross-functional projectsDeliver accurate project plans and budget evaluations for validation activitiesEssential RequirementsMaster’s degree in Biotechnology, Chemistry, Biology, or a related scientific fieldProven experience in packaging and closure integrity within the pharmaceutical or biotechnology industryA minimum of 5-10 years’ experience in packaging and engineering roles especially primary packaging from a scientific perspectiveAbility to assess material-product interactions (e.g., reactivity between product and plastic container, or if glass or paper is more suitable)Strong knowledge of GMP, validation principles, and regulatory frameworks (EU GMP, ISO13485, 21 CFR 820)Demonstrated ability to lead investigations using root cause analysis toolsFluent in English and French (written and spoken)Additional InsightsLocation: Verviers, Belgium – Hybrid (3–4 days onsite per week)Contract Type: Full-time, permanentStart date: ASAPInterested?Send your CV to Khanyi Mabena at k.mabena@panda-int.com or contact her directly at +32 280 88622 to learn more about this opportunity.