Duties & Responsibilities:
Ensure BMRs are complete and the necessary data are recorded in PC for PQR
Follow up of proper documentation of training records.
Prepare PQR on products produced.
Prepare/ review BMRs/BPRs for products and submit for approval.
Revise formats and submit to immediate supervisor for check and approval.
To collect samples from validation batches at each sampling stages.
Conduct the necessary test parameters on the samples.
Ensure that samples of validation batches are submitted/ taken to QC lab.
Participate in cleaning validation methods.
Participate in validation of analytical methods.
To perform IPQA activities and record results as needed as per the procedure, when assigned/ required.
Report to immediate supervisor on the daily analysis activities.
Compile Report QA activities on weekly and monthly basis.
Preparation of QA SOPs.
To perform any other activities assigned by the department head from time to time.
Suggest any ideas for implementation that may help on the improvement of quality system
Job Requirements
Requirement: Bachelor of Pharmacy
Experience: More than 4 years (Pharmaceuticals company experience is Preferable) or related field.
Type of Employment: Permanent
Salary and Other Benefit Packages: Attractive and can be determined with negotiation based on the candidate’s previous earning, qualification and competency.
How To Apply
The company provides excellent growth opportunities to deserving candidates. Efficient professionals willing to take giant stride along with the Group are invited to apply within 10 days, clearly marking on the Job Title to:
Fikirte.cadila@gmail.com.Or Oromia region, sheger city Gelan wereda or A.A Meskel flower behind Tulip International Hotel Bamuk Building 2nd floor.
Cadila Pharmaceuticals (Ethiopia) PLC
P.O. Box 571 Code 1250, Addis Ababa, Ethiopia
