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