CSV / Validation Consultant

Onsite, Zealand ASAP Until the end of the year, with the possibility of extension

Om stillingen

We are looking for a CSV / Validation Consultant for a PAS-X project with a focus on documentation, compliance, and traceability.

Short description:

– Experience with PAS-X validation in a GMP/pharma environment.

– Responsible for URS, FS/DS, RTM, IQ/OQ/PQ, and audit-ready documentation.

– Review and approval of PAS-X and test documentation in accordance with regulatory requirements.

– Ensuring end-to-end traceability between requirements, configuration, and testing.

– Coordination of validation activities, including handling deviations and risks.

Start: ASAP

Duration: Until the end of the year, with the possibility of extension

Location: Onsite on Zealand

If this sounds like an opportunity for you, please send your CV to Emilia Rønn Olsen at emilia@dba-consult.dk or contact her at +45 53 52 88 99.