google.com, pub-2091334367487754, DIRECT, f08c47fec0942fa0 IPC Specialist -Alexandria at Pharaonia Pharma- Bourj Alarab, Alexandria

IPC Specialist -Alexandria at Pharaonia Pharma- Bourj Alarab, Alexandria

 IPC Specialist -Alexandria at Pharaonia Pharma- Bourj Alarab, Alexandria

IPC Specialist -Alexandria at Pharaonia Pharma- Bourj Alarab, Alexandria


“IPC Specialist -Sterile-Alexandria”


About Pharaonia
Pharaonia Pharmaceutical is one of the top 30 pharmaceutical companies in the Egyptian market going to be one of the top 10 companies within years based on its new outstanding system and environment.

What You’ll Do


Ensure that all workers in the sterile area are following the standard operating procedures.
Ensure that raw materials enter the production areas in the correct manner in accordance with standard operating procedures.
Ensure that the weights of the active ingredients for each batch are correct before the start of the preparation process in accordance with the batch records.
Ensure that all tools, containers, and clothing are washed and sterilized in accordance with standard operating procedures before preparation and filling process.
Ensure that no deviations occur during the preparation process, and if they do, the appropriate action is taken.
Ensure that no deviations occur during the filling process, and if they do, the appropriate action is taken.
Ensure that samples are taken for each batch in accordance with the scheduled times recorded in the batch records.
Ensure that the inspection process is proceeding in accordance with standard operating procedures.
Ensure the efficiency of the ampoule inspection process before release.
Ensure that the work at the WFI treatment plant is proceeding in accordance with standard operating procedures.
Ensure the calibration status of all equipment inside the sterile area, whether internal or external.
Follow up on the implementation of verification and validation work then prepare the reports for them.
Follow up on the cleaning, disinfection, and sterilization work in the sterile area in accordance with standard operating procedures.
Receive batch records from production after all manufacturing stages have been completed.
Review batch records before submitting them to the archiving department.
Review and approve production records during the manufacturing stages in the sterile area.
Conduct acceptance tests for new individuals in the ampoule inspection department.
Train and approve new individuals on aseptic area gowning procedures.

Applicants should possess the following qualifications to go through initial screening:


Bachelor of science, department Chemistry / Physics
Computer literate / Fluent in English
1-2 years of experience in pharmaceutical analysis
skill (high accuracy – alertness – precision in working with described
tools-methods system )
Information decadency, logical thinking & computer skills

Apply Here

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