Document Facilitation Expert
1 week ago
Key Responsibilities
- Edit and format GMP documents, including Specifications, SOPs, and Technical Documents.
- Facilitate the routing of technical documents through required workflows.
- Review documents for grammatical errors and formatting.
- Cross-training in other areas of ASO-GxP Biologics as needed.
- Support clinical work through data management of release and stability samples within the PDLIMS system.
We offer a competitive salary of $65,000 - $85,000 per year, depending on experience, along with a range of benefits and opportunities for growth and development.
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