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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Temporary / NonExempt position.

• Experience managing documentation for a Quality Department.
• Should be a Document Control Program Specialist and have technical skills.
• Willing to take ownership of the document control program.
• Will prepare, edit, file, and assemble documentation such as reports or technical documents, records, or correspondence. 
• Maintains numerical, alphabetical, chronological and/or subject filing system. 
• Responsible for file maintenance and record keeping; locates and removes file material upon request.

• Bachelor in Science 
• 2-5 years of experience in the Quality area

• Temporary /long term /hourly position
• Send resume, preferable in Word format.