Analyze validation test data to determine whether systems or processes have met validation criteria or to identify root causes of production problems. Conduct Risk based verification for GxP (GMP, GCP, and GLP) systems and laboratory equipment. Participate in medical device manufacturing processes including production and packaging. Write IQ/OQ/PQ Protocols and summary reports. Identify gaps, defects and deviations encountered while executing validation protocols and provide resolution and appropriate CAPAs. Conduct validation or qualification tests of new or existing processes, equipment, or software in accordance with internal protocols or external standards. MINIMUM REQUIREMENTS: MASTER'S DEGREE OR A FOREIGN ACADEMIC EQUIVALENT IN SCIENCE, PHARMACY, CHEMISTRY, BIOMEDICAL, ENGINEERING (ANY), TECHNOLOGY( ANY) OR RELATED. IN LIEU OF ABOVE WILL ALSO ACCEPT A *BACHELOR'S DEGREE OR A FOREIGN ACADEMIC EQUIVALENT IN SCIENCE, PHARMACY, CHEMISTRY, BIOMEDICAL,ENGINEERING (ANY), TECHNOLOGY( ANY) OR RELATED WITH 5 YEARS OF RELEVANT EXPERIENCE IN THE JOB OFFERED OR AS A ENGINEERING PROFESSIONAL ORRELATED FIELD.ANY SUITABLE COMBINATION OF EDUCATION, TRAINING AND EXPERIENCE IS ACCEPTABLE. JOB LOCATIONS IN ISELIN, NJ AND VARIOUS UNANTICIPATED CLIENT SITES IN THE US THAT REQUIRES TRAVEL AND RELOCATION TO THESE SITES.To apply, Mail Resume to: In Response to Job Order _, Intellectt Inc., 517 Route 1, South Suite 1115, Iselin, NJ, 08830. Apply before Job Order closes.