QC Document Specialist

3 weeks ago


Cambridge, United States The Steely Group Full time
Job DescriptionJob Description

Our client is looking to add a Quality Document Control Specialist to their team on a contract basis. 

Responsibilities:

  • Veeva GxP documentation and archival
  • Processing, Sorting, Organization and archival of on-site GxP archives and digital archives
  • Projects related to GxP documentation
  • Assist with the administration of GxP training


Requirements /  Qualifications:

  • Bachelor's degree in Science (preferred)
  • 0-2 years experience
  • Attention to detail
  • Highly organized
  • Eager to learn
  • GxP
  • Document Control and Management
  • Training
Company DescriptionThe Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire & Contract Consultants) and Retained Executive Search.Company DescriptionThe Steely Group is a national preclinical, clinical, and commercial staffing firm and certified women’s business enterprise. We partner with small, growing biotech, pharma, and gene therapy companies to help bring treatments to patients by providing flexible talent acquisition solutions including Contingent Search (Direct Hire & Contract Consultants) and Retained Executive Search.
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