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:

• In this role you will be responsible for adhering to and ensuring compliance with cGMP principles and maintain them in effective manner.
• Perform in-process quality check activities according to SOP in production / packaging departments (Tablets/Capsules/liquids/Semi solids/Injectable) in complying with cGMP principles and captures test results in batch records.
• Check the required tests for all products during production / packaging process.
• Inspect and check incoming materials by confirming specifications and return unacceptable materials.
• Revise all documents for in process control and perform a quality review of logbooks.
• Responsible to revise and document for inspection results and complete all required documents for in process control by completing reports and logs, summarizes re-work and waste, and inputs data into quality database on SAP system.
• Participate in Internal Audit programs.
• Preparation of Annual Product Quality Review reports.
• Responsible for Deviations and Market Complaint investigations and ensure implementation of CAPA lifecycle.
• Ensure the in-process check equipment’s are adequately calibrated and functions properly.
• Perform and check the line before start (production/packaging) and give the clearance for the work.
• Maintain accurate records and perform tests on all activities conducted in the plant.
• Maintain safe and healthy work environment by following standards and procedures and complying with regulations.
• Perform Self-inspection runs in his areas

QUALIFICATIONS:

• Bachelor’s degree in science/ pharmacy
• Minimum of 2 Years experience
• Good Computer knowledge and knowledge of QMS system “Agile, Trackwise, Ampelogic”
• Proficient in English.
• Quality and Business decisions taker
• Good Knowledge and command on cGMP
• Risk Assessment knowledge
  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

Please refer the Job description for details