Sr. Quality Control Consultant Temporary 1 Yr (1361)

By Posted in - on August 17th, 2017 0 Comments
Adante Staffing Inc. Published: December 14, 2017
Cambridge, MA


Responsibilities include: 

  • Review all Quality Control (QC) related documents in support of finished drug products, drug substances, and stability samples, including specifications, method validation and stability protocols and reports from CMO's and CRO's
  • Write, review, and approve Change Controls, CAPA’s, QC deviation reports, and participate in out of specification (OOS) and out of trend (OOT) investigations where required


  • BS/MS w/ 5+ yrs working in analytical QC GMP
  • Expertise with Quality management systems
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