QRC group is a firm dedicated to provide services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

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Responsible for validation documents project deliverables, execution of tasks,
status reporting, project completion and good technical writing skills.  Develop
strategic approach and detailed plan for the remediation (short and long term)
for manufacturing process.

BS/MS degree in Science, Engineering or a related subject with experience with five (5) years  experience in CSV Life Cycle (CSV, IQ, URS, FS, FRA, TM, OQ, PQ) for Laboratory, Manufacturing and packaging equipment in a cGMP's environment. Self-starter, with the capability to work independently, setting goals and achieving milestones with minimal direction.  QUALIFIED CANDIDATES SEND RESUME IN WORD FORMAT.

Available to work as independent contractor for a six months project in  Fort Worth, Dallas, Texas

QRC Group is an EEO employer.