This is an exciting opportunity for an experienced Qualified Person to join successful global biotech based in the Netherlands.
My client is currently looking for a Qualified Person to become a strategic part of their Dutch Quality Assurance department. This is a senior position for a business oriented experienced QA Manager listed as QP in a European Country.
The ideal candidate has a science degree or higher, with at least 10 years experience in an industrial pharmaceutical R&D environment and has acted as QP before.

Responsibilities:

To perform the duties of a Qualified Person in line with international requirements to enable the release of products on a regular basis

Ensure batch release is done in accordance with current GMP regulations, the Product Specification Files and the requirements of the Quality Assurance Agreement.

To advise on day to day quality related issues encountered on site including deviations, change controls, CAPAs etc.
Maintain and improve continuously the quality system and related documentation system, according to GMP and GLP regulations.

Increase the awareness on relevant quality related matters for management and employees, by providing advice, assistance on critical issues and training

If you are a QP and you are interested in working in the Netherlands, Please forward your CV to Nasiya Sharmarke by clicking on the "Apply" button or alternatively call us for further information and a confidential discussion on this opportunity