Job Information
SHOOLIN, INC. VALIDATION ENGINEERS in ISELIN, New Jersey
Perform validation projects in support of equipment, product process and cleaning validation. Write and review validation protocols, validation reports, and cleaning procedures. Involve in Cleaning Validation, Equipment Validation, and Process Validation Programs to support cGMP pharmaceutical manufacturing operations. Perform protocol execution of CIP and COP cleaning validation, product process and cleaning continuous verifications. Perform workflow analysis and lay out facilities to maximize safety, output, quality, and profitability. Perform GAP analysis of previous executed protocols. Generate equipment characterization reports, FMEA studies. Involve in preparing compliance reports about existing status of the cGMP, GCP and GLP. Master’s degree in Science, Technology, or Engineering (any) with 1 year of experience in the job offered or related occupation is required. Work location: Iselin, NJ and various unanticipated locations throughout the U.S.Send Resume to HR Dept., Shoolin, Inc., 120 Wood Avenue S, Suite 611, Iselin, NJ 08830.