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

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

The candidate will work in a CSV project for a pharmaceutical manufacturing environment, and will be responsible for documents, project deliverables, execution of tasks, status reporting, and project completion. Must have good technical writing skills.

• Bachelor Degree on Computer or Industrial Engineering or Science
• 5 years+ experience in CSV life cycle; Equipment Qualification for Packaging areas; IQ, OQ, PQ; Validation Plan and Reporting; Protocol Execution
• Computer literate; excellent writing skills; bilingual Spanish and English; self-starter, team oriented.

QUALIFIED CANDIDATES SEND RESUME IN WORD FORMAT VIA EMAIL

All your information will be kept confidential according to EEO guidelines.