QA logistic specialist in Raron

h3Quality Assurance Specialist Logistic Specialist /h3 pbLocation: /b Visp, Valais, Switzerland /p pbContract Duration: /b 6 months /p pbStart Date: /b Immediate availability required /p pbIndustry: /b Pharmaceutical / Biotechnology /p pbLanguages: /b Fluent English and German (mandatory) /p h3About the Role /h3 pWe are currently seeking an experienced bQuality Assurance Logistic Specialist - Raw Materials /b to join a leading pharmaceutical and biotechnology manufacturing environment in bVisp, Valais /b. This is an excellent opportunity for a quality professional with a strong GMP background and proven experience in raw material qualification, supplier management, and material release activities. /p pThe successful candidate will play a key role in ensuring the compliant receipt, qualification, release, and supplier management of raw materials while supporting GMP-compliant manufacturing operations. /p h3Key Responsibilities /h3 ul liPerform incoming raw material verification in accordance with applicable GMP procedures and quality standards. /li liManage the qualification and release of raw materials used in manufacturing processes, including physical verification and release activities within LIMS. /li liEstablish, maintain, and monitor approved raw material suppliers, SOPs, and quality systems. /li liReview and manage supplier change notifications and quality alerts. /li liInvestigate and manage material-related deviations, non-conformances, and change controls. /li liMonitor and collect KPIs associated with raw material qualification and release activities. /li liEnsure accurate and compliant documentation and data management. /li liEscalate critical quality issues and potential compliance risks in a timely manner. /li liCollaborate closely with Manufacturing, QC, Supply Chain, and external suppliers to ensure uninterrupted operations. /li liSupport continuous improvement initiatives related to raw material management and supplier quality processes. /li /ul h3Required Qualifications /h3 ul liBachelor's degree in Life Sciences, Chemistry, Biotechnology, Pharmacy, or a related scientific discipline. /li liMinimum b3 years of confirmed experience /b in Quality Assurance within the pharmaceutical or biotechnology industry. /li liStrong knowledge of GMP regulations and quality systems. /li /ul h3Experience with: /h3 ul liRaw material qualification and release /li liSupplier quality management /li liDeviations, CAPAs, and Change Controls /li liLIMS systems /li liQuality risk assessment /li /ul h3Language Requirements /h3 ul libEnglish: /bFluent (mandatory) /li libGerman: /bFluent (mandatory) /li /ul #J-18808-Ljbffr