Senior QA Specialist, Global Document Control Management
Revolution Medicines · Redwood City, CA
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Role summary
Revolution Medicines seeks a Senior QA Specialist to oversee global document control and management systems for an oncology company. The role involves developing GxP-compliant processes, managing electronic document management systems, and driving continuous improvement across the organization.
What they're looking for
- BA/BS in Biological Sciences, Chemistry, or related field with equivalent experience
- Minimum 5 years pharma/biotech QA experience in GxP environments
- Experience developing and implementing GxP quality systems
- Direct experience managing global GxP document management and training systems
- Working knowledge of GxP requirements, regulatory standards, and ICH guidelines
- Hands-on experience with Veeva QualitySuite platforms (QualityDocs, Training, QMS)
- Strong oral and written communication skills; proficiency with Microsoft Office
What you'll be doing
- Develop, implement, and improve global GxP Document Management Program ensuring regulatory compliance
- Review and coordinate Document Change Controls and workflows for controlled documents
- Serve as subject matter expert for electronic Document Management System optimization and governance
- Partner cross-functionally to evaluate document processes and implement sustainable improvements
- Monitor and analyze document lifecycle metrics, driving corrective and preventive actions
Privacy & handoff
This role links to Revolution Medicines's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.