Duties and Responsibilities:

Ability to take and perform routine validation, quality assurance, and other related job assignments as may be necessary for execution of the project.

Ability to read basic Engineering drawings -- P&IDs, Process and Utility Flow diagrams, HVAC diagrams, Equipment drawings and Instrumentation drawings.

Ability to work with equipment in the field including basic hand tools, lift reasonable weights, read, prepare and analyze data for development of reports.

Experience in the utilization of various temperature monitoring devices, including Kaye dataloggers.

Experience in development of IQ, OQ, PQ, Standard Operations Procedures, and Summary documents.

Experience in execution of IQ and OQ protocols for systems.

Requirements:

B.S. or B.A. degree in engineering, science or related fields.

Three-to-five years experience in design, process control, construction, commissioning, validation for Pharmaceutical or Healthcare industries

Working knowledge of FDA GMPs, FDA guidelines, European guidelines and other regulatory requirements.

Knowledge of MS Office Suite, database, and spreadsheet software packages.

Knowledge of development of protocols for validation of process or laboratory equipment, utilities, associated control system, ability to develop Installation, Operational and Performance qualification documents.

Willingness to travel within the continental United States as well as other countries as may be required for duration of up to 12 months.

Effective written and oral communication skills.

Send your resumes to P.O.Box 712, Piscataway, NJ-08854.

email to: resumes@valoitinc.com