Manage end-to-end project accounting for assigned accounts, including contract-based billing, collections, cash application, expense processing, reconciliations, and financial reporting while maintaining accounting controls and accurate.
Provide CSA and CSV expertise for GxP systems across Pharmacovigilance, Clinical, and Regulatory Affairs, guiding validation, lifecycle compliance, and risk-based system oversight.
Lead pharmaceutical deviation and out-of-specification investigations, determine root causes, and develop defensible, risk-appropriate CAPA plans that meet data integrity standards and regulatory expectations.
Supports Veeva Vault eTMF migration from planning through validation and post-go-live stabilization, ensuring clinical documents and metadata are accurately migrated and compliant with GxP requirements.
Author and execute commissioning, qualification, and validation documentation for equipment, systems, software, and processes; run and document tests, maintain records, and perform I/O testing on automated manufacturing equipment.
Page 1 · 5 results
