Location: Hoofddorp
Duration: 1 year (extension is possible)
Language: English
Industry: Pharma
Start date: 01/02/2023
The company
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 perform a variety of QA activities t ensure compliance with applicable regulatory requirements.
Responsibilities
-Maintain programs and processes to ensure high quality products & compliance with current Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP)
-Compile product binders as preparation for QA disposition and QP release
-Identify and report deviations
-Contribute to the Quality on the floor processes, including GEMBA walks
Requirements
-A minimum of 2 years of experience in a QA role or similar
-Knowledge of the Current Good Manufacturing Practices (cGMP)
Do you recognize yourself in this position? Do not hesitate to apply.