1. To check quarantine areas of all sections for unidentified, unsealed, or delayed Batches.
  2. To inspect daily all parameters concerning cleanliness, equipment quality, and Maintenance of the concerned record.
  3. To ensure daily the line clearance of packing lines of all areas i.e. packing hall, Belladerma, Zinco, Arsoplast and coating at each changeover.
  4. To control the handling of nonconforming products/materials by segregation and Identification, and ensure that the nonconformity is rectified before further processing.
  5. To review and retain batch manufacturing records along with retaining samples till one year after expiry.
  6. To monitor in-process parameters of production batches and processes like Adhesive mass, and thread counting for care gauze.  
  7. To assess the wastage record of all products and identify the root cause of excessive wastage.
  8. To monitor and carry out sampling of raw materials (active/Inactive) & packing materials as per SOP.
  9. To check raw data and other reports generated by Quality Control to ensure compliance with GMP.
  10. To monitor and carry out in-process sampling of intermediate products and delivery in the QC department  per SOP
  11. To ensure that raw materials and finished goods, released for use/sale, have been appropriately released.
  12. To check the environmental monitoring and keep it recorded as per SOP
  13. To encourage teamwork in all departments for the achievement of the Quality Objectives of the Company technically.
  14. To suggest recommendations for continual improvement of QMS.
  15. For effective implementation of the Quality policy of Arsons Pharmaceuticals, perform duties as per SOPs related to QMS.
  16. To execute the tasks given by the management.
  17. Ensure daily personnel hygiene and keep it recorded.
  18. Immediate replacement of other QA officer and perform  his/her Jd’s
  19. Maintain environment-friendly procedures to improve environmental health.
  20. Provide a safe working environment by supporting healthy, safe and secure programs.
  21. To ensure the preparation of the dossier for new products. As well as collect data form the product, QC, and purchase departments to comply dossier.
  22. To ensure that after check and review from the relevant department dossier is submitted to the Regulatory manage.

Job Details

Functional Area:
Total Positions:
1 Post
Job Shift:
First Shift (Day)
Job Type:
Job Location:
Gender:
Male
Minimum Education:
Pharm-D
Degree Title:
Pharm-D/BS chemistry degree from any institute recognized from HEC
Career Level:
Entry Level
Minimum Experience:
1 Year
Apply Before:
Feb 21, 2025
Posting Date:
Jan 20, 2025

Arsons Pharmaceutical

Pharmaceuticals / Clinical Research · 1-10 employees - Lahore

We feel that the biggest strength we have is that we are an organization created specially in response to an environment of health care demands. By the grace of God Arsons Pharmaceutical is successful in fulfilling our commitment and responsibility towards the poor and down trodden citizens of our country, by providing excellent quality medicines at an affordable cost.

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