Duration: 1 year (extension is possible)
Start date: 15-11-2022
Our client is a biopharmaceutical company engaged in the development of cancer immunotherapies with the aim to provide long term response and eliminate this chronic disease.
About the role
As a Quality Assurance Specialist you will be responsible for ensuring compliance with applicable regulatory requirements.
-Perform quality reviews of manufacturing batch records generated on paper and electronic systems
-Review manufacturing and environmental monitoring to ensure high quality products with GMPs & GLPs
-Provide support for deviations investigations and CAPAs
- 2+ years’ experience in a regulated environment
- Advanced level of English communication
- Ability to effectively communicate with peers.
Ready for the next step in your QA career? Reach out to me by applying to this vacancy.