To organize the quality police system in the factory, preparing the
requirements of the quality system, supervising the quality system, applying
GMP regulations, releasing finished product batches & approving batch records,
specifications and SOPs (the candidate must be holding B. Sc of pharmacy)
Train, evaluate & motivate subordinates in quality assurance
Prepare, review and approves SOPs concerning QA.
Review all the SOPs, formats, logbooks …etc of all departments.
Approve batch records and release the product batches.
Organize the training in the factory at various levels and take part in
instructing GPM training.
Evaluate & validate suppliers of raw materials and packing materials
and achieve the approved once.
Approve the master formula, specifications and analytical methods for
Prepare a plan for internal auditing of all departments, write and
approve the requested report& follow up the corrected subjects.
Participate in validation, organizing the validation team.
Investigate the claimed materials.
Approve the deviation repots for raw material packing materials,
finished products, production parameters & in process control analysis.
Approve the certificate of release for the finished product.
Receive and review the release certificates coming out from QC
department for raw materials and packing materials.
Receiving and review the batch records and certificates of analysis of
Handling complaints, product recalls and batch recalls and batch
All candidates must have had 5 year experience at a reputable
pharmaceutical company as Quality assurance managers
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