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 seeking a QA Specialist to provide quality oversight for manufacturing operations, validation activities, facilities, and environmental programs, ensuring compliance with GMP standards and regulatory requirements.

• Doctorate or Master’s + 2 years of Scientific experience; or Bachelors + 4 years of Scientific experience.
• Experience performing batch record (EBR) review, approval, and reconciliation.
• Oversight manufacturing operations.

• Manage events and decision making.

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