I am currently partnered with a top global pharmaceutical company with a very Robust Pipeline. They are leading the market in innovative new products for pharmaceuticals.
They are seeking an CSV Consultant to join their team on a Min. 8+ months contract w/extension possibilities.
Location: New Jersey
- Background in developing full validation documentation and testing protocols (IQ/OQ/PQ/UAT) in the many SDLC phases.
- Multiple years' experience in GxP / QA within FDA regulated environments GAMP 5 with risk-based CSV is required.
- Assist in the oversight for the Computer Systems and Software Validation.
- Support advanced technical quality needs in specific CSV circumstances, Such as validation of latest systems, upgrades, changes, or rectification etc.