QA Logistic specialist

Visp, Valais, Switzerland
100% On-site (5 days/week)
6-Month Renewable Contract
Start Date: September 2026
About the Opportunity
Our client, an international company operating in the biopharmaceutical sector, is currently looking for an experienced
QA Logistics & Materials Specialist
to join its Quality organization in Visp.
In this role, you will act as a key quality representative supporting material management, incoming material verification, raw material qualification, and supply chain quality activities within a highly regulated GMP environment. You will work closely with Quality, Supply Chain, Warehouse, Procurement, and Manufacturing teams to ensure compliance, continuity of supply, and operational excellence.
Key Responsibilities
Perform incoming material verification in accordance with GMP requirements and internal procedures.
Support the qualification, approval, and release of raw materials used in manufacturing operations.
Maintain and manage material-related data and documentation within quality systems.
Ensure supplier-related information and material records remain accurate and up to date.
Coordinate and manage supplier notifications, quality alerts, and material-related changes.
Support investigations related to deviations, non-conformances, CAPAs, and change controls.
Monitor and report KPIs linked to material qualification and release activities.
Ensure timely escalation of critical quality issues impacting materials, logistics, and supply chain operations.
Collaborate with Supply Chain, Warehouse, Manufacturing, Procurement, and Quality teams to maintain GMP compliance and operational efficiency.
Contribute to continuous improvement initiatives aimed at strengthening quality and logistics processes.
Required Qualifications
Bachelor's degree in Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
Minimum 3 years of proven experience in QA Logistics, Material Quality, Raw Material Quality, or Supply Chain Quality within a GMP-regulated pharmaceutical, biotechnology, or life sciences environment.
Strong knowledge of GMP regulations and pharmaceutical quality systems.
Hands-on experience managing deviations, CAPAs, investigations, and change controls.
Solid understanding of raw material qualification, incoming inspection, material release, and supplier quality processes.
Experience working with SAP, SAP QM, SAP MM, LIMS, or equivalent systems.
Strong analytical thinking and problem-solving capabilities.
Excellent communication and stakeholder management skills.
Fluent English is required.
German is an advantage.
Ideal Profile
Experience operating at the interface between Quality Assurance, Supply Chain, Logistics, and Manufacturing.
Ability to prioritize tasks and manage multiple activities in a fast-paced GMP environment.
Strong attention to detail and compliance mindset.
Proactive, solution-oriented, and capable of working independently.
Comfortable interacting with cross-functional and international teams.
Applications that do not meet the minimum experience requirements or do not demonstrate relevant QA Logistics experience will not be considered.
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