Job Description

*This role requires on site presence and is open to candidates in the EU*

I am currently supporting a pharmaceutical/biotech manufacturer that is looking for an experienced Computer System Validation (CSV) Engineer for a 6-month freelance project .

The role will involve supporting validation activities for GxP-regulated computer systems, including documentation, IQ/OQ/PQ execution, compliance checks, and alignment with regulatory expectations.

What we’re looking for:

  • Strong background in CSV within pharma or biotech
  • Experience with IQ/OQ/PQ
  • Ability to work independently and manage deliverables
  • Familiarity with GxP environments and validation documentation
  • Availability for a freelance/contract engagement

If you're open to new projects and have relevant CSV experience, feel free to message me directly or share your CV.

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