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!

Responsible for providing Quality oversight to ensure that operations for licensed pharmaceutical products are manufactured, tested, and stored, according to current Good Manufacturing Practices (cGMP) and other applicable regulations.

• Review and approval of Electronic Batch Records and related documentation to support Drug Substance Disposition Process.
• Performs SAP systems transactions to support batch processing and disposition requirements.
• Strong knowledge of and experience with processes involved in manufacturing, QA, QC, validation and process development
• Demonstrate ability to interact with regulatory agencies.

EDUCATION / EXPERIENCE

• Bachelor’s degree in Life Science or Engineering
• 5 years of Manufacturing or Quality in GMP regulated environment experience

Qualified candidates should send resume in Word format.