Pharmaceutical QA Compliance SME

Trenton, NJ

Job ID: 125502 Industry: Pharma


Pharmaceutical QA Compliance SME

Project Description:

Our client is a pharmaceutical company who is looking for assistance with their document review for all of their GCP QA compliance. They will be traveling to clinical trial sites to review all of their documents from a quality standpoint

  Day to Day Responsibilities:

The consultant must have extensive GCP experience within a clinical trial setting for quality asssurance. The client is looking for someone to come on site and review all of their paper based quality compliance and documentation records within GCP. This person must come from a Drug background and have specific experience with oral solid dosage and tableting. They will be conducting investigations and deviations as well as CAPAs based upon their findings. The consultant may have to travel to different sites throughout the east coast to help review their documentation. The consultant must have a GCP (Good Clinical Practices) drug background and have recently been conducting investigations and document review for a drug company.

Required Skills:
  • QA Compliance
  • Investigations, Deviations, Capas
  • GCP, Clinical Background
  • Drug products

Job Type: Contract  

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