Our client is a professional Pharmaceutical organization, based in Noord-Brabant Netherlands. International pharmaceutical company which has a big location in The Netherlands from where they serve around 50 countries.
You will provide QA oversight for the clinical products that they recieve and distribute.
Responsible for completing the Receipt Approval process for incoming Investigational Medicinal Products.
Compliance review and approval of clinical label artwork.
Participate in ABR internal audits as needed.
Assist in the development and delivery of GMP training activities.
Bachelor or Master degree in Life Sciences
Around 3 years of related QA experience
Fluent in English (Dutch is not a necessity)
Familiar with GMP, GDP and / or GCP