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  • Location

    Zuid Holland, Netherlands

  • Job title:

    GMP Documentation Expert

  • Sector:

    Biotechnology, Pharmaceutical

  • Job ref:

    44830

  • Startdate:

    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