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Job Description
- Managing the deviations received from different departments, investigation & root cause analysis & review of reports to be approved by QA manager.
- Management of CAPA system, ensure that all approved CAPAS are tracked and communicated to all concerned parties & manage the follow-up of CAPA plans implementation and effectiveness.
- Managing change control system, evaluation of changes & checking appropriate implementation.
- Issuance of product quality review plan and reports annually for all products.
- Handling and investigation of customer complaints till closure
- Creation and update of a plan for quality risk management in production areas, warehouses & Quality control, ensure that all potential and existing quality risks are tracked, Review quality risk management reports to be evaluated and approved by Quality Assurance Manager.
- Reviewing the layouts of production departments, warehouses & QC labs (classes, differential pressure, material flow, personnel flow and airflow).
- review and update the major documents like Site Master File, Company Manual and Quality Policy.
- Ensure compliance with GMP pharmaceutical guidelines and ISO Standards, Quality Management System and Data Integrity
- Supervision of vendor management / supplier evaluation system including raw/ packaging materials suppliers, toll manufacturers, Bio-equivalence centers and other service providers.
- Handling external audits from different local and external regulatory bodies and licensors.
- Managing quality agreement with suppliers to ensure all contractual quality requirements are fulfilled.
- Implement the system for qualification of outsourced activities s and suppliers according to pre-set criteria and follow up annual performance to issue updated approved list.
- Responsible for Internal audit program, plan issuance and execution, follow up of CAPA implementation.
- Handling cases of Recall (if any) according to approved system and procedures
Job Requirements
- Bachelor of pharmacy or science.
- (5-9) year of experience.
- Experience in QA compliance and GMP standards for Pharmaceutical and Nutraceuticals products.
- Computer knowledge
- Attention to detail
- Proficiency in the English language
- Proficiency in MS Office (MS Excel)
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