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  • Location

    NOORD HOLLAND, Netherlands

  • Job title:

    QA Documentation Specialist

  • Sector:

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The Company 
Our client is a pharmaceutical organization located in Hoofddorp, Noord-Holland. This company focuses on the development of cancer immunotherapy. 

Role Description 
In this role you will be responsible for the maintenance of the document management system for the QA department. 

- Scan and store the documents to defined electronical repository.
- Process documents through relevant workflows of electronical document management system as QA-DC.
- Support controlled document issuance for operations.
- Archive the scanned documents.

- At least Bachelor's Degree in Pharmacy or similar. 
- 2+ years of experience in a QA or Documentation Specialist position. 
- 1+ years of experience working in a GMP environment. 
- Excellent organization skills and eye for detail. 
- Ability to work independently under minimal direction. 

Other information
For more information please contact Carla Garcia at or +31 (0) 20 658 98 01.