Company:Safe Pharma

Department:Quality Control



In-Process Control specialist QC


1. Examination and analysis of premixes and any intermediate product done in the production area. 2-Preparing laboratory chemicals. 3-Performing of the process validation for all methods of preparation of all medicines in the production process.

Job requirements:

Functional Roles:

* Writing methods of analysis for all intermediate products and premixes.

Writing all standard working methods for managing In-Process control and updating them.

Analyzing the intermediate product, medicine and premixes done by the production and recording the results in the records for the analysis and issuing certificates for analysis.

Analyzing the internal preparations used in the manufacture of medicine and recording the results in the records for the analysis and issuance of certificates Own analysis.

Review the calibration dates for the devices that are calibrated internally in the laboratory and make the necessary calibration for them for the analysis devices that are It is according to standard working methods.

sampling of all capsules and medicine and premixes done in the production area at time intervals to analyze it.

General Roles:

1-Application of occupational safety and health rules at work.

2-Apply the rules for preserving the environment while working.



Bachelor degree in Faculty of science or pharmacy  .


  0:2 QC labs


Communication and teamwork

Quality and attention to details 

Years of Experience: 1

Posting Date: 11 May 2023

Application End Date: 11 June 2023

Available Vacancies: 1

Job Level: Specialist

Function: QC - In Process Control