Job title: Freelance Quality Control professional
Contract: 6–12 months | Extension likely
Key skills: Quality Control, GMP, Method Validation, Laboratory Systems, Documentation, Pharma Manufacturing
We are currently looking for an experienced freelance Quality Control professional to join a vibrant and innovative working environment. You will play a pivotal role in overseeing the safety monitoring and quality control related to clinical trials and marketed products. You will contribute to ensuring patient safety, regulatory compliance and effective management of pharmacovigilance activities within cross-functional teams and maintain the highest standards of safety reporting. This role supports an ongoing QC project and offers the opportunity for a long-term assignment within an award- winning, top-performing company.
Typical scope of work
QC laboratory support within GMP-regulated environments
Method validation and verification activities
Review and approval of QC documentation and protocols
Supporting laboratory investigations and deviations
Ensuring compliance of laboratory processes and systems
Audit and inspection readiness support
The exact scope will vary depending on the project.
Background we are looking for
Experience in Quality Control laboratories within the pharmaceutical industry
Strong knowledge of GMP guidelines
Comfortable working independently in a project-based setup
Fluent English (spoken and written)
French and/or Dutch is an advantage, not a requirement
Interested?
If you would like to be considered for current or future freelance QC 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.
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