QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

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• Experience in Process Validation Life-Cycle.
• Experience in Laboratory Equipment Validation Life-Cycle
• Should be able to generate validation documentation like PQ protocols and reports.
• Should be able to write proficiently in English
• Should have experience in generating and reviewing SOP’s
• Willing to learn and effective team player
• Organized and willing to work on scheduled dates (Non-Standard Shift)
• Proficient in Microsoft Office (Word, Excel, Power Point)

• Bachelor’s degree in Life Sciences or Engineering and 5 years of Scientific experience OR 
• Master’s Degree in Life Sciences or Engineering and 3 years of Scientific experience

• Able to work as Independent Contractor and in a Non-Standard Shift.
• Qualified candidates should send resume in Word format.