Documentation Specialist II – GMP (19-00528) – NJ – Bridgewater


  • This position is involved in numerous activities regarding the cold chain hand sampling function. 
  • Maintaining equipment inventory and manual equipment change authorization process.
  • Assemble/analyze all supporting documents for internal review.
  • Coordinate receipt of TMD acceptance documents and prepare for NAQ authorization.
  • Work with Sample Operations partner on remediation of issues, when applicable
  • Coordinate all documentation associated with the Sales Professional Certification
  • Program and prepare for NAQ authorization to receive samples and begin sampling.
  • Review equipment qualification test documentation, including calibration records, to support equipment releases for GMP use.
  • Perform administrative functions to support documentation filing, storage and retrieval .


  • Proficient in MS Office – Excel, Word, Outlook 
  • Must possess sound interpersonal and information gathering skills. 


  • College Pharma experience preferred

Source: Job Diva – Job Listing

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