This project aims to strengthen validation governance across global FMCH operations, covering process, cleaning, equipment, utilities, laboratories, and computer systems, to ensure compliance with cGMP, FDA, WHO, ISO and GAMP 5.
- Validation specialist with 10 to 15 years experience in pharmaceutical and/or FMCG environments
- Direct experience designing and executing validation protocols (IQ/OQ/PQ)
- Proven experience writing validation reports and core validation documentation
- Experience developing and maintaining validation standards, SOPs, and validation master plans
- Demonstrated work under cGMP, FDA, WHO, ISO, and GAMP 5 requirements in regulated environments
- Proven track record leading and managing site-level or multi-site validation projects (planning, execution, documentation)
Mandatory hands-on experience in:
- Process validation
- End to End complete validation lifecycle
- Computer system validation (CSV)