Responsibilities

• To ensure that gowning and entry / exit procedure are followed.

• To give line clearance for sampling, dispensing, manufacturing and packing process.

• To carry out in process checks for sampling, dispensing, manufacturing and packing process. 

• To verify the batch manufacturing and batch packing records for its completeness.

• To review of master BMR/BPR.

• To carry out monthly calibration of IPQA instrument in the entire facility.

• To prepared store and retrieve documents related to Standard Operating Procedures documents.

• To maintain the control samples (Retention Samples) of finished product. 

• To carry out sampling of intermediate and finish product.

• To check, correct and maintain the artwork document.

• To maintain regulatory records and fulfilling legal requirements 

• To review of master BMR/BPR (Blank and filled). 

• To report daily to the superior to appraise about activities carried out, any deficiencies observed and appropriate corrective action taken or to be taken.

• Preparation of Product Quality Review.

• Preparation of Process Validation Protocol and report and execution of Process validation Activity.

• Conduction of Training Program.

Department: Quality Assurance

Job Requirements

Qualifications:

Educational Qualification: 

• B. Pharma.

Total years of experience: 

• 5 years

How to Apply

Interested and qualified applicants should send their CVS via email: yonas.a@africurepharma.com\adisu.genene@africurepharma.com