New Jersey All, NJ
QA Validation Engineer
Responsible for Compliance and validating equipment, systems, and processes in support of biopharmaceutical manufacturing in accordance with FDA, GMP and related parameters
Responsible for reviewing, revising and approving qualification/validation protocols and reports for facilities, processes, and equipment.
B.S. in Engineering or related with 3+ years of validation experience in biopharmaceutical, GMP/FDA regulated facility.
Experience in authoring validation protocol and reviewing validation and qualification reports
Understanding of quality systems, CAPAs, Investigations, Root Cause and related Quality measures