Description:
We are a national staffing firm and are currently seeking a QA Document Control Specialist for a prominent client of ours. Details for the position are as follows:
Job Description:
- The QA Document Control Specialist will work to develop, deploy, and support the Veeva Quality Document System, manages, and tracks all GMP documentation.
- Following SOPs, the incumbent is responsible for adhering to the document lifecycle procedures and archives all records in accordance with the records retention schedule, as well as retrieving all documents as requested.
- Manage and maintain controlled documents in Electronic Document Management System (EDMS) ensuring documents go through controlled documents life cycle in accordance established procedures.
- Processing documents in the EDMS, issuance logbooks, notebooks, and batch records.
- Provide documentation support during audits and regulatory inspections.
- Experience in working with documentation in a regulated industry. Advanced Microsoft Office skills (Outlook, Word, Excel, PowerPoint)
- Knowledge of Good Manufacturing Practice (GMP) concepts and guidelines and document control systems/activities.