The Global Quality Auditor GCP is responsible for ensuring compliance with Good Clinical Practice (GCP) across global clinical activities. The role includes planning and executing risk-based GCP audit...
Consultant Immunoassay Development (Diagnostics | Neurodegenerative Diseases)Contract: Temporary / Consultant roleLocation: Ghent, BelgiumAn established diagnostics company active in neurodegenerative...
Role DescriptionWe are seeking a highly specialized Bioengineering Process Scientist to support biologics and gene therapy programs within a leading global biopharmaceutical organization.This role ope...
Senior Analytical Validation & Q&V SME (MSAT / PAD / QC)Liège, Belgium – 3-month contract (Hybrid, extension highly likely)Job DescriptionYou will join a GMP analytical and MSAT environment supporting...
The Quality Control Analyst operates within the OPEX team in a pharmaceutical manufacturing environment. The role focuses on executing, optimizing, verifying, and validating analytical methods for raw...
QA Lab SupervisorJob DescriptionIn this role, you will be responsible for:Establishing and maintaining strong working relationships with partners in Quality Control (QC) laboratories, as well as with ...
C&Q SME (Commissioning & Qualification Subject Matter Expert)Objectives and ResponsibilitiesThe function holder:Supports the C&Q group in providing documented evidence that all equipment and utilities...
Quality & Compliance Associate (Junior) | Global Pharma | On Site RoleJob DescriptionA global pharmaceutical manufacturing site is seeking a junior Quality & Compliance Associate to support and contri...
Process Validation Engineer – Cell Therapy | CAR-T (EMEA)Our client is active in the development, manufacturing, and commercialization of CAR-T cell therapies in partnership with a leading biotechnolo...
Immunoassays Development Senior ScientistWe are supporting a diagnostics company in the search for an R&D Senior Scientist with strong hands-on expertise in immunoassay development, particularly on au...