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  • Location

    Zuid Holland, Netherlands

  • Job title:

    GMP Documentation specialist

  • Sector:

  • Job ref:

    44536

  • Startdate:

    2020-08-03

The company:
Our client is one of the global leader in healthcare and pharmaceutical products, with base in Leiden.The company focuses on the discovery, development, manufacture, and marketing of vaccines to protect people worldwide from infectious diseases.

Job description: 
The GMP Documentation specialist will be the first point of contact within the production teams for questions related to cGMP (training,
inspections, audits and documentation).

Responsibilities:
  • Maintenance and improvement of the available cGMP systems
  • Initiating and handling of compliance records 
  • Supporting/leading in keeping process documentation up-to-date
  • Coordinating training system within the department

Requirements: 
  • Bachelor or Master level of education
  • 3 years of relevant experience, including with change controls, non-conformances and CAPA records
  • Experience with cGMP and EHSS standards is required
If this is something you are interested in, please contact me at d.cantore@sire-search.com or at +31 20 658 98 00.
 

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