QA Documentation Specialist

Highly Competitive Salary
  1. Permanent
  2. Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GVP)
  3. United States
North Chicago, USA
Posting date: 11 Feb 2021

Proclinical is currently recruiting for a QA Documentation Specialist with a biopharmaceutical company located in North Chicago, IL.

Job Responsibilities:

  • Provide QA support for manufacturing process
  • Documentation management
  • Ensure all products are in compliance with corporate and government regulations
  • Support of quality regulations
  • Conduct initial regulatory review and approval of quality documents
  • Perform QA review of product release

Skills and Requirements:

  • HS diploma or higher
  • 1-4 years of experience
  • Past experience within pharma/biotech industry and QA
  • Excellent interpersonal skills
  • MS Office, especially Excel
  • Attention to detail is critical for processing
  • Experience with AttachePro would be a plus
  • Document management/control experience

If you are having difficulty in applying or if you have any questions, please contact Catherine Nguyen at 215-531-5643.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.