Vacature (Sr.) Qualified Person (ref. 1609)
Vacaturenummer 1609
Regio Noord-Holland
Uren per week 40

(Sr.) Qualified Person (ref. 1609)


Qualified Person wanted! 


Information available upon request.

De functie

As Qualified Person you will be responsible for providing GMP compliance, reviewing documentation, releasing recorded batches for clinical research products. You will also be involved in GMP non-compliance situations as well as deviations and complaints according to appropriate regulations and legislations. You will work in conjunction with the quality and regulatory departments.

Wat vragen wij?

Master degree in Pharmaceutical Sciences, or relevant.

Experience in the pharmaceutical, life sciences, chemical sector(s).

Experience within the pharmaceutical industry with QMS.

3-5 years’ experience in GMP with an understanding of production and QC. 

IMP experience and sterile experience is advantageous.

Versatile, motivated and takes initiative.

Good computer skills.

Excellent verbal and writing skills in English.

Dutch is a pre.

Wat bieden wij?

Conditions of employment are up to the market standard.


Jay Baktawar
+31 (0) 88 035 1993


Please send your application through our website.