This role supportsGLP/GMP microbiology analyses within a flagship biotech development program,leveraging advanced analytical technologies in a flexible, agile, andcollaborative lab environment. Reporting to the LabManager, Global Analytical Development, this position contributes to themicrobiology laboratory by executing GLP and GMP analyses. It interfaces withQA, GAD (all functions), and manufacturing colleagues to enable smooth analysisexecution,
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
1. April 2026
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