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Job Description
- Prepare validation activities plans & issue protocol that comply with regulatory requirements & company policy.
- Witness and follow-up validation run execution, collect all necessary data and register and assess any anomalies.
- Issue validation report, communicate validation outcome with management and concerned stakeholders and archive reports.
- Register, communicate & assess any changes will be conducted in site prior change execution & track execution of change actions.
- Prepare NCR reports, deviation and NCR risk assessment & review CAPAs relevant to validation activities.
- Register & evaluate identified current or potential quality risks, suggest with key stakeholders proper mitigation actions & re-evaluate risk after their implementation.
- Provide periodical reports to superior with appropriate analysis regarding all validation updates to ensure effective & accurate updated records.
- Fulfill other related tasks as asked by management and as arising from the business.
Job Requirements
- B.Sc. Degree in Pharmaceutical Science, Science or Engineering.
- 3-6 Years of Experience in related functions Preferred Pharmaceutical industry or FMCG.
- Excellent command of English
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