GMP Documentation Specialist - (Libertyville, IL)

The primary responsibilities would be document review and creation, mostly from Quality Assurance and GMP documents from the manufacturing floor. You will be working with batch records and creating documents. They ae completely paper based and are looking to go electronic. They are on schedule to start commercial manufacturing in about a year and the longterm for this role is to become an auditor once the documents have all been created and they start manufacturing.