The Company 
Our client is one of the global leader in healthcare and pharmaceutical products, with base in Leiden. The company focuses on the discovery, development, manufacture, and marketing of vaccines to protect people worldwide from infectious diseases.

Role Description 
You will be responsible for the cGMP production of Clinical Trial materials (CTM). Apart from production operations you will be updating documentation, be responsible for predefined process steps, and the state of related equipments.

Responsibilities 
- cGMP production of CTM material
- Updating documentation
- Responsible for the state of related equipment 
- Involved in innovation projects 
- Data management

Requirements 
- MBO or HBO degree in the L:ife Sciences 
- Min. of 2 years of Pharma GMP experience 
- Experience working as a technician or operator in a cGMP environment 

Other Information 
For more information please contact Ece Karakurt at e.karakurt@sire-search.com or +31 (0) 20 658 98 01.