Bio-Pharmaceutical Document Control Specialist

Boston, MA

Job ID: 126305 Industry: Pharma

Bio-Pharmaceutical Document Control Specialist

Project Description:

Our client is a bio-pharmaceutical therapeutics development company looking for a quality assurance consultant to conduct batch record reviews. 

Day to Day Responsibilities:

The client is looking for a quality control professional to conduct batch record reviews specific to drug substances and API. This person must have experience working with small molecules and active pharma ingredients as it relates to drug substances. They must understand all drug substance good manufacturing processes associated with these active ingredients to accurately analyze data. Their duties include reviewing and analyzing all documents and data associated with over fifteen batches. They will be analyzing data associated with lab tests, IPCs, and HPLCs as it relates to wet chemistry.

Required
  • Batch Record Review Experience
  • Small Molecules Experience
  • Drug Substance Experience

Job Type: Contract  

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