Pharmaceutical QMS Lead

Boston, MA

Job ID: 129448 Industry: Pharma

Pharmaceutical QMS Lead


Project Description:

Our client is in the pharmaceutical industry and in the middle of a large integration project where they are merging two control documentation systems. They are looking for a QMS Lead that can review and edit documents in Veeva. 


Day-to-Day Responsibilities

This person will be responsible for gathering, editing and reviewing  documents within subject areas, and archival of the material. They will be working independently in the document management system, which is Veeva. The majority of the work will be editing and reviewing documents that will be passed off from the technical writers. Under the head of QMS, this person will be expected to work with cross functional teams through their R&D document harmonization. This person must have great communication skills and the ability to lead content experts through the development of multiple procedural documents simultaneously.  It would be a plus if this person had clinical R&D experience, but it is not required. 


  • 8+ years Procedural Document Development
  • Pharma experience
  • Veeva  or other specific Doc Control System Experience
  • Cross Functional Lead Experience


Clinical R&D


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