- Implementation and follow up of the validation & qualification systems.
- Process validation.
- Cleaning validation.
- Review analytical method validation.
- Review calibration plans, follow its execution and issue balances calibration plans & execute them.
- Machines and equipment qualification and re-qualification.
- Issue & maintain annual validation master plan & validation protocols.
- Review calibration certificates and follow up execution of calibration plans.
- Participate in the deviations, OOS investigations & audits as required.
- Any additional work that is requested by his superiors.
B.Sc. of Pharmacy or science.Not less than 3 years of experience in similar position.Male is preferable.Good understanding of the rules and guidance of ISO, GMP and GDP.Attention to details.Problem solving skills.Active learning.Time Management skills.Professional using Microsoft office