Banner Image
  • Location

    Zuid Holland, Netherlands

  • Job title:

    GMP Documentation Expert

  • Sector:

    Biotechnology, Pharmaceutical

  • Job ref:

    44830

  • Start Date:

    2020-09-01

The company
Our customer is one of the biggest producers of vaccines in the world. The company uses its extensive and innovative technology to combat life-threatening diseases such as Corona, HIV and Ebola. 

Role description 
As a GMP Documentation Expert you will be mainly responsible for the maintenance and improvement of the available cGMP systems + ensuring the process documentation is up-to-date.

Responsibilities:
  • Point of contact for questions related to GMP (training, audits and documentation) 
  • Handling compliance records (Change Control, nonconformances and CAPA records)
  • Root cause analysis 
  • System ownership of general production processes like gowning, routing and flow, segregation  

Requirements:
  • BSc with 3 years of proven experience in the pharma/biotech industry
  • Experience with Change Controls, nonconformances and CAPA records
  • Experience with Veeva truVault is preferable 
  • Lean Green Belt is a plus 

Other information
Are you interested and want to apply for this role? Please fill out your application via the apply button below and contact Guilherme Tokunaga.
Contact Us

SIRE LIFE SCIENCES B.V.

Staten Bolwerk 1
2011 MK Haarlem
The Netherlands
+31 (0) 20 658 9800

SIRE STAFFING SOLUTIONS B.V.

Keizersgracht 440A
1016 GD Amsterdam
+31 (0) 20 658 9804

SIRE LIFE SCIENCES DEUTSCHLAND GmbH

Theatinerstraße 11
80333 München
+49 (0) 89 3803 8966

SINCERE. INTELLIGENT. RESULT-DRIVEN. EXCELLENCE.