The IVF Guide is seeking a Validation Engineer for a fixed-term contract (6–9 months) to lead the writing and formalisation of the validation documentation suite. This is a documentation-focused, office-based role: the scientific lead will run experiments, and you will translate results into fully compliant validation protocols and reports.
The ideal candidate will have strong PCR-based diagnostic experience, ideally with DDP, and a track record of producing validation documentation to ISO
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