We are now looking for a resource on the validation side of things going on here. Depending on the resource were looking for someone with (LabVantage) LIMS and quality systems validation experience and/or general more broad Pharma/Biotech CSV experience that could back-fill as staff augmentation.
Engagement would be (at least) through the end of the year.
Potential in-scope activities.
i. CSV/Lab Systems Qualification document/deliverable authoring.
ii. Test script/protocol authoring (potential execution).
iii. SOP modification/authoring.
iv. Spreadsheet Validation.
For the right person: local/hybrid/on-site remote and offshore would all be considered.
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