QC - In-Process Control Specialist

Summary:

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:

• 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.

• Preparing the laboratory chemicals required for analysis and reviewing their expiration dates.

• 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.

• Preparing the standard solutions and standard samples required for analysis.

• Do diffraction reports. For medicine and intermediate products that do not conform to specifications.

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

• Perform process validation for all the processes for medicine and premixes preparation in the production.

• Application of occupational safety and health rules at work.

• Apply the rules for preserving the environment while working.

• Fulfill other related tasks as asked by management and as arising from the business.

Qualifications:

B.Sc. degree in Science.

Years of Experience: 1

Posting Date: 18 October 2021

Application End Date: 30 November 2021

Available Vacancies: 3

Job Level: Specialist

Function: QC - In Process Control

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