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Pharmaceutical Manufacturing
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Job description

At Julphar, we are on a journey of culture transformation & our mission is to provide a better quality of life for the entire family by delivering best in class solutions and real value with compassion and professionalism.


Our core values: Respect, Collaboration, innovation, Integrity and Compassion - Combined with a focus on diversity, inclusion, and equal opportunities - are key drivers in our aim to make a positive impact on the lives of the patients we serve, enable Talents , create a healthy work environment, and accomplish our goals through world-class research and with the compassion and commitment of our employees.


Detailed Job Description


  • The main responsibility of the role holder is to adhere with the cGMP principles and to maintain them in an effective manner.
  • Responsible to coordinate with batch review team (Receiving and distribution of batch files and updating the tracker).

Core Competency


  • Responsible for receiving of manufacturing documents from all Julphar sites
  • Responsible for receiving of Packaging documents from Physical Lab
  • Making entry of Batch details in the release tracker
  • Coordinating with Quality control to receive COA prior to release
  • Compiling of Manufacturing and Packaging documents
  • Deliver the Batch Documents after release for Archiving
  • Perform any other work assigned by the Team Leader/ Manager Batch Release

Qualification/Functional Knowledge


  • Bachelor’s in computer science
  • Advanced knowledge in MS-office (Word & Excel)
  • Proficient in English
  • Proven understanding and well-disciplined while dealing with all stakeholders.
  • Excellent knowledge of reporting procedures and record keeping.
  • Total Experience 3 Years.

We value people from different backgrounds. Could this be your story? Apply today or visit www.Julphar.net to read more about us and the journey of Julphar


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