Job Summary
A clinical and scientific staffing company is searching for a person to fill their position for a Remote Biotechnology and Pharmaceutical Quality Assurance Document Contractor.
Core Responsibilities of this position include:
- Reviewing/editing draft procedures and other documents for compliance with templates, use of Microsoft Styles, typos, etc
- Checking reports for compliance to regulatory style guide, minimum required approvers, and data verification
- Reviewing and performing QC checks on external documents and executed records added to EDMS
Skills and Requirements Include:
- 3-4 years of related experience
- Working knowledge of current Good Manufacturing Practices (cGMP)
- Experience using Microsoft
- Styles and electronic document management systems
- Strong verbal and written communication skills
- Able to work independently
