Are you an experienced Quality Validation SME in the pharmaceutical industry? Apply now!
More information available upon request.
– Quality validation SME for projects and changes related to Computerized Systems.
– Creating, reviewing, approving validation deliverables.
– Validation of MES (Werum PAS-X).
– Minimum 5 Years’ experience in Validation/Quality Role in GMP setting.
– Experienced as Quality Validation SME.
– Professional level of English, written and spoken.
– Open to high pressure turnaround of documentation.
– Willing to work extra time as required.
The employment conditions are up to market standard.
+316 2125 4820
Please send your application through our website.