Documentation Review and Sample Management Specialist

Complete data integrity review of analytical data reporting records for the client’s portfolio, which includes Synthetic molecules, Peptides, and BioproductsSupport development stability studies which include handling, storing, delivering samples, and documenting per relevant proceduresAssist domestic and international shipping of material, such as development samples or consumablesMust be able/authorized to handle Controlled Drugs or Controlled Substances under the guidance of DEA requirements