*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

*Responsibilities: ***

·        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***

*With Regards*
*Kamal Pandey*
*IT Recruiter*
Ask IT Consulting
You Ask We Deliver!
*Phone : 631-869-4700,** **Fax : 631-803-4488*
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