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 employeesJob Summary/Main PurposeTo adhere with the cGMP principles and to ensure effective measures taken for Good Documentation practices in Batch Documents.Responsible for leading Batch review & release, Finished product retention samples and shipping complianceTo ensure the effective measure taken for the good Documentation practiced in the batch documentsKey Responsibilities & Key Result Areas
Responsible for leading Finished products release and ensure that the activities are performed as per approved procedure
Responsible for leading the Batch document audit and finished product documents/retain samples checking group and ensure that the activities are performed as per approved procedures and in a timely manner.
Responsible for leading the Shipping group for final checking of shipment before shipping
Responsible for training the Batch review team to ensure a robust review process
Responsible to take UD decision after completion of the complete Batch document review
Responsible to approve shipment under quarantine forms provided by the Sales/Tender departments as per the approved procedure
Responsible to communicate with Cross functional departments if any discrepancies found in the batch.
Responsible for evaluating employee performance as per HR regulations
To perform any other responsibility assigned by QA - Director / CTO