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!

We are looking for a qualified Validation Specialist with experience in GMP-regulated environments and pharmaceutical processes.

• 1 to 5 years of experience in a GMP environment.
• Experience in the pharmaceutical industry.
• Knowledge of and experience with aseptic and regulated processes.
• Experience developing and executing:
  • Validation protocols.
  • Validation reports.
  • SOPs (Standard Operating Procedures).
  • Statistical data analysis.
• Ability to work on multidisciplinary projects and comply with regulatory requirements.
• Bilingual (English ans Spanish)

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