About the Company
We 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 Role
The consultant will work closely with internal stakeholders to ensure quality standards are consistently met.
Responsibilities
* Performing Quality Assurance activities within GMP-regulated environments
* Quality Assurance (QA)/ Quality Management Systems (QMS)
* Risk/ Deviation Management GMP Compliance
* Reviewing batch documentation and supporting product release
* Managing deviations, investigations, and CAPAs
* Supporting audits and regulatory inspections
* Ensuring compliance with applicable quality and regulatory standards
Qualifications
* Demonstrated experience in Quality Assurance within the pharmaceutical industry
Required Skills
* Strong knowledge of GMP guidelines
* Ability to work independently in a freelance, project-based role
* Fluent English (written and spoken)
Preferred Skills
* French and/or Dutch is an advantage
Pay range and compensation package
Contract: 6–12 months | Extension possible
Equal Opportunity Statement
If 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.