Related skills
document management gmp veeva vault qms audit readiness📋 Description
- Provide ~20 hours/week of QA admin support across docs, complaints, and reports
- Prepare, format, and maintain QA documents in Veeva Vault
- Coordinate document lifecycle including review and version control
- Ensure adherence to internal doc standards and audit readiness
- Support complaints management and data entry for regulatory records
- Assist in CMO scorecard data collection and reporting
🎯 Requirements
- Bachelor’s degree in Life Sciences, Biotechnology, Chemistry, Engineering, or related field
- Approximately 5 years in a life sciences QA environment
- Experience supporting QA and QMS activities
- Strong knowledge of GxP (GMP, GDP) and regulated docs
- Document creation, formatting, and lifecycle mgmt in DMS (Veeva Vault)
- Experience with complaints management and audit-ready records
- Attention to detail with accurate, traceable records; stakeholder interaction
- MS Office proficiency for data consolidation and reporting
Meet JobCopilot: Your Personal AI Job Hunter
Automatically Apply to Healthcare Jobs. Just set your
preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.
Help us maintain the quality of jobs posted on Empllo!
Is this position not a remote job?
Let us know!