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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• Strong knowledge of and experience with processes involved in manufacturing, QA, QC, validation and process development.
• Demonstrate ability to interact with regulatory agencies.
• Ability to evaluate compliance issues.
• Project management skills.
• Strong skill in working independently and to effectively interact with various levels.
• Strong organizational skills, including ability to follow assignments through to completion.
• Initiate and lead cross functional teams.
• Enhanced skills in leading, influencing and negotiating.
• Collaborate and coordinate with higher level outside resources.
• Strong word processing, presentation, database and spreadsheet application skills.

• Doctor OR Master’s degree in Life Science or Engineering and
  3 years of Manufacturing or Quality in GMP regulated environment experience OR 
• Bachelor’s degree in Life Science or Engineering and
  5 years of Manufacturing or Quality in GMP regulated environment experience

• This is a Non-standard shift position (able to work on Administrative, second and third shifts).
• Willing to work as independent contractor.
• Candidates should send resume in Word format.