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About the CompanyWe are currently supporting a pharmaceutical organisation in Belgium that requires an award winning, experienced freelance Quality Assurance Consultant to support an ongoing GMP-regulated project. This assignment offers the opportunity to work within a structured, quality-driven company, contributing to the delivery of compliant pharmaceutical manufacturing activities.About the RoleThe consultant will work closely with internal stakeholders to ensure quality standards are consistently met.ResponsibilitiesPerforming Quality Assurance activities within GMP-regulated environmentsQuality Assurance (QA)/ Quality Management Systems (QMS)Risk/ Deviation Management GMP ComplianceReviewing batch documentation and supporting product releaseManaging deviations, investigations, and CAPAsSupporting audits and regulatory inspectionsEnsuring compliance with applicable quality and regulatory standardsQualificationsDemonstrated experience in Quality Assurance within the pharmaceutical industryRequired SkillsStrong knowledge of GMP guidelinesAbility to work independently in a freelance, project-based roleFluent English (written and spoken)Preferred SkillsFrench and/or Dutch is an advantagePay range and compensation packageContract: 6–12 months | Extension possibleEqual Opportunity StatementIf you would like to be considered for current or future freelance Quality Assurance opportunities, please send your CV and phone number.We aim to respond as quickly as possible. Due to high volumes, this may not always be possible for every application. Rest assured, we will retain your details and contact you should a suitable opportunity arise.
