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Job Description
- Supervising and managing the Quality Assurance Department to ensure that the company's products conform to the specifications.
- Establishing quality terms, policies and procedures and explaining them to the employees and workers, training them and motivating them to work with it.
- Issuing regulations and instructions related to the application of these procedures and following up their implementation.
- Following up the implementation of the quality system in all departments of the company and ensure that the factory operating system conforms to the rules of good operation cGMP and other quality systems such as: ISO 9001, ISO 14001.
- Discussing the daily problems facing production departments and laboratories, and developing appropriate solutions for them.
- Make the final release of the raw materials received by the company after verifying their validity in accordance with the standards and controls stipulated in this regard.
- Make the final release of the company's products after verifying their validity and compliance with the specifications and the standards and controls stipulated in this regard.
- Coordinate with the production, warehouse and engineering sectors to run the work, and solve daily problems to ensure the quality of the product and the efficiency of performance.
- Assuring quality of systems' documents.
- Assuring efficiency of operations' documents.
- Following up on quality and environment projects in the company.
- Following up the internal and external inspection of the company's facilities and departments.
- Administer supervision of the departments and units of quality assurance, solving the problems of employees and motivating them.
- Finalizing approval of the results of samples analysis after ensuring their accuracy and validity.
- Determining specifications for raw materials, packaging materials, intermediate products and final preparations with the managers of other departments in the factory in accordance with international and pharmaceutical standards, and monitoring the extent to which these materials conform to the established specifications.
- Following up the results of biological control of raw materials, intermediate products, final preparations and qualitative and interim control of preparations, and work to ensure that the preparation conforms to the required specifications.
- Implementing the company's environmental policy, and ensuring that the system is applied in the sector.
- Reviewing laws and regulations related to environmental dimensions, and working to update them.
- Adopting environmental programs and following up on their implementation, and working to increase environmental awareness.
- Reviewing environmental documents and their amendments, as well as environmental measurements, and ensuring their compliance with the law, and working on correcting them on a regular basis, and ensuring their conformity.
- Submitting periodic reports on the achievements and challenges to the higher management.
Job Requirements
- Graduated from the Faculty of Pharmacy.
- At least 15 years of experience in pharmaceutical factories.
- Super knowledge of advanced scientific management systems and methods.
- Superior ability to lead and direct, and the ability to solve problems and work difficulties.
- Full experience in the field of drug production and Good Manufacturing Practices.
- Knowledge of laws and regulations governing work.
- Proficiency in English and computer systems.
- Outstanding managerial and communication skills.
