Jr Specialist - QA

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.

Key Responsibilities

• Perform line clearance and release activities according to established Standard Operating Procedures (SOPs).
• Conduct in-process quality checks on products during manufacturing and packaging, adhering to prescribed timelines.
• Accurately record test results in batch documentation and monitor the overall process.
• Ensure the correct materials and components are used in production and packaging, following specifications outlined in BMR (Batch Manufacturing record), BPR (Batch packaging record), MFM (Manufacturing Formula), MPI (Master Packaging Instructions), MIV (Material Issue Voucher), or Dispensing Sheets.
• Maintain compliance with Good Manufacturing Practices (cGMP) in the work area. This includes monitoring documentation practices, verifying the accuracy of batch records, logbooks, labels, etc.
• Verify proper gowning attire, cleanliness, and adherence to SOPs, manufacturing instructions, and packaging instructions.

• Ensure environmental conditions (temperature, humidity, and differential pressure) meet the requirements for the product and the work area.
• Verify that in-process check equipment is properly calibrated and functions as intended.
• Assist in preparing the Annual Product Quality Review (APQR) for products as per established procedures.
• Participate in both internal and external audit programs.
• Handle tasks related to the Quality Management System (QMS) at the worksite.
• Conduct investigations into quality-related issues like deviations or complaints.
• Manage Corrective Action and Preventive Action (CAPA) processes within the Ampelogic system.
• Perform other duties as assigned by the QA Operations Team Leader
  
  

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  Good on process compliance and good command in English.
• Responsible in approach & high on accountability and ownership.
• Good in Time & Task Management
  
  

• Bachelors Degree in Pharmaceutical or similar.
• 0-2 year s experience in QA IPC functions.
• GMP (Good Manufacturing Practices) and science Knowledge.
• Functional Knowledge In-process (Production and Packaging) and Quality Assurance.
• Proficient in MS Office (Word & Excel).