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