*QA Validation Engineer***
*West Chester**, PA***
*Contract - 6 months***
· 7+ years GCP exp. (can be combination of GMP/GLP/GCP but need solid
GCP auditing experience)
· General QA background
· Strong knowledge of FDA regulations/guidances, ICH guidances,
corrective action plans, etc.
· Willing/able to travel
· Exp. with pharma, manufacturing, distribution, shipping will be
· Conducting CRO and clinical site audits (very hands-on)
· Mostly external audits
· GCP compliance/Rectifying non compliant issues
· Developing corrective action plans.
· Extensive travel.
*Possible 40-60% travel***
Ask IT Consulting
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