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!

• Experience auditing manufacturing processes and / or documentation, preferably in sterile / parenteral operations. 
• Read and write in English is a must.
• Able to work a non-standard 2nd-3rd shifts.

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

• Send resume preferable in Word format

• Willing to work as Independent Consultant in a non-standard 2nd-3rd shifts.