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!

• Commissioning & Qualification 
• Process Validation
• Quality Management of GMP Documents and Batch Related Records 
• QA Operations Oversight (i.e. “on the floor” Quality oversight, troubleshooting and decision making during activities execution) 
• Hands on experience on Parenteral / Biological DP Manufacturing
• Experience on Drug Product Aseptic Processing

• Bachelor’s degree in Sciences/Engineering and
  5 years of directly related experience or
• Doctorate degree or Master’s degree in Sciences/Engineering and
  3 years of directly related experience

• Non-Standard Shift.
• Willing to work as Independent contractor.
• Send resume in Word format.