CSV / Validation Consultant

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

Om stillingen

Stillingen er besat. Dette er et tidligere opslag. Vi modtager ikke længere ansøgninger til denne opgave.

Se aktuelle opgaver eller læs om vores konsulentnetværk.

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.

Ansøg

Ønsker du at søge stillingen, eller har du spørgsmål kan du kontakte Emilia Rønn Olsen og høre nærmere. Hvis du ansøger pr. mail, så husk at vedhæfte dit CV.