For one of our clients, an international pharmaceutical company, we are seeking a Clinical Supplies Quality Specialist.General Information:Start date: ASAPLatest possible start date: 03.08.2026End Date: 31.07.2027Workplace: Schachen, LuzernHome office: possibleWorkload: 100%Working hours: StandardAbout the work:The Clinical Supplies Quality team is responsible for release of the packaged and labeled drugs for usage in clinical studies. The team is
Role Overview: Specialist QC ComplianceThe Specialist QC Compliance acts as a Subject Matter Expert (SME) responsible for ensuring that Quality Control (QC) processes adhere to regulatory requirements, cGMP expectations, and site procedures. The role focuses on driving continuous improvement, maintaining data integrity, and managing quality events within a fast-paced biotechnology or pharmaceutical environment. Key ResponsibilitiesQuality Systems
Join a fast-growing Bioplant in Yverdon-les-Bains during a pivotal expansion phase. We are seeking a QA QC Expert to ensure the highest quality standards for our Drug Substances and Raw Materials.ResponsibilitiesBatch Disposition: Collect and review all records for Drug Substance (DS) and Drug Product (DP) release; chair weekly disposition meetings.QA Oversight of QC: Provide day-to-day quality guidance to the lab, approving specifications, analytical
Über unseren KundenUnser Kunde ist ein international führender Engineering-Spezialist für hochperformante thermische Energielösungen. Mit Fokus auf ökologische Nachhaltigkeit entwickelt und wartet das Schweizer Traditionsunternehmen komplexe Wärme- und Kältesysteme für industrielle Grosskunden weltweit. Als Pionier in der Dekarbonisierung trägt das Unternehmen massgeblich zur Reduktion von CO?-Emissionen bei und begleitet Projekte über den gesamten
19. mars 2026
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