- Job Summary:
Responsible for performing basic tasks and some standardized routine
testing and maintaining a high level of quality sections 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