Major Purpose

• 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.
• 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.

Required Number: 4

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.

Work Place: Gelan Factory.

Education and Experience

• BSc. Degree in Pharmacist from a recognized College University
• Minimum of 2 Year Experience in Supervisor and Related area

Skills

• Excellent oral and written communication skill.
• Strong analytical and problem-solving skill.
• Basic knowledge of MS Office, words, excel, internet etc.
• Willingness to learn, improve and adapt to changing requirements.