Job Summary:
Responsible for performing basic tasks and some standardized routine testing
and maintaining a high level of quality section services by monitoring and
recommending solutions to quality-related issues under close supervision.
Job Description:
* Ensuring compliance of manufacturing processes at Hikma plants with current Good Manufacturing Practices (cGMP) and guaranteeing plant facilities and machinery conformity to regulations, safety procedures and quality standards through developing internal policies and guidelines and ensuring compliance of internal policies to regulatory standards, as well as reviewing related documents and reports for validation and approval.
* Performing other duties related to the job as assigned by the direct supervisor
* Maintaining the quality of production within an acceptable level by guaranteeing the compliance of production, packaging, and warehouse activities to cGMP
* Approving the transfer of finished products to the following stages after checking their conformity to quality standards
* Following up on internal and external audits to ensure compliance with quality standards and regulations
* Developing policies and standards and establishing operating procedures to manage the flow of work
* Ensuring the implementation of policies, codes, and pharmaceutical regulations to guarantee high-quality production levels
* Ensuring that workers follow safety procedures as required, in addition to ensuring the implementation of regulatory rules and procedures while handling pharmaceutical waste
* Following up on the implementation of process validation plans while monitoring and observing process validation activities
* Participating in the implementation of Quality Assurance (QA) protocols and reviewing prepared QA reports
* Reviewing updated QA guidelines and ensuring that existing SOPs are being updated taking into consideration the changing work requirements and operations, and new trends and policies to to attain quality objectives
* Conducting daily plant checks, observing, and recording results in addition to always ensuring clean plant facilities and guaranteeing that employees follow safety procedures as required and handling waste
* Identifying raw material quality protocols and standards and assisting QA Officer in checking the conformity of raw material to set specifications
* Resolving complications that may occur at the main plant and recommending calibration of machinery as needed to achieve the required level of products quality
* General Knowledge in Aseptic Techniques.
Job Qualifications:
* B.SC in Pharmaceutical Science or Science.
* 1-2 years of experience in sterile and solid area
* Preferably (Cairo, Obour, New Cairo, Nasr City, Heliopolis, Badr, Zagazig, Sharqiyah, and 10th of Ramadan) residents
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