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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. 

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


Requirements
- 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 g.tokunaga@sire-search.com or apply directly below.