QA Documentation Specialist

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.

#LI-CN1