Description
A CSV Engineer is required to join a Global Pharmaceutical company based in the Netherlands. The suitable candidate will be working in their IT department responsible for the production part of the project. The main objective of the role is to support equipment validation and conduct periodic reviews; as well as being responsible for the implementation of the validation strategy.The Role:
* Responsible for the qualification and validation of computer based manufacturing and laboratory systems.
* To work in accordance with EU GMP and FDA standards.
* Responsible for requalification and implementation of validations, including offering full support to internal and external departments with the validation reports.
Skills / Experience:
* A strong background working in the Pharmaceutical or Biotech industry.
* Experience of working with IT systems or application management.
* Experience of implementing validation and qualification reports.
* Good English and Dutch language skills both spoken and written.
To learn more about this excellent and rare opportunity to join a prestigious Pharmaceutical organisation and fulfil a unique and rewarding role, please send in your current CV.