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The Company 
Our client is a biotech and pharmaceutical organisation, based in Noord-Brabant Netherlands. In this site, they are responsible for the packaging of drugs and the distribution of them across the whole EMEA region. 

Role Description 
As a CQV Engineering (packaging) you will be leading the development of commissioning, qualification and validation of packaging operations. You'll also be updating various validation documents such as System Level Critical Assessments. 

- Creating Commissioning, Qualification and Validation plans 
- Performing risk assessments 
- CQV summary reports 
- Conducting CQV tests 

- Hands on Commissioning and Qualification experience with Secondary Packaging Operations 
- Experience with Secondary Packaging Systems, incl. experience with Print and Inspection systems (e.g. Systech, Cognex) 
- Min. of 4 years of experience performing CQV activities for manufacturing pharma companies (GMP)
- CSV experience is a big plus 
- Basic knowledge of Paperless validation systems (HP ALM/ KNEAT)

Other Information 
For more information please contact Guilherme Tokunaga at or apply directly below.