AVS is looking for a Technical QA Validation resource for work in a bioPharma facility.  This is a long term position. This role is responsible for reviewing validation documentation for a facility renovation project which is currently ongoing. A person in this role would be responsible for reviewing all validation deliverables – IQ, OQ, PQ protocols and reports for equipment (both lab systems and manufacturing) and facility change documentation. Minimum 2 years of work experience and a degree are required.