Developers sought for CSV validation work in a large-scale new facility.
Assist cross-functional teams with Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) tasks.
This role requires knowledge of regulatory guidelines, including FDA 21 CFR Part 11 and EU Annex 11. A background in computer system validation is necessary, preferably within the pharmaceuticals or biotechnology sectors.
Familiarity with risk-based validation approaches will be valuable to this position.