United States onlySupport the end-to-end lifecycle management of R&D controlled documents for a big biopharma leader, ensuring compliance with regulatory standards and internal quality procedures.
Requirements
- Coordinate and manage controlled document workflows
- Track documentation milestones and follow up with contributors
- Provide technical editing and proofreading support
- Conduct thorough QC reviews for regulatory, procedural, and formatting compliance
- Maintain and update document templates
- Support audits and inspections by preparing documentation and ensuring inspection readiness
- Collaborate with stakeholders and cross-functional teams to resolve document-related issues
Benefits
- Contingent Worker (Contract, W2)
- 12 months contract length with possible extension
