Specialist QA; QC oversight

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.

• Monitoring and ensuring current Good Laboratory Practices (GLP) and Good Documentation Practices (GDP) followed by laboratory personnel during a routine operation to ensure adherence to procedure.
• Investigating the “Out of specifications” reported for Finished products, Stability samples, Raw Materials and Packaging Materials.
• Investigation of “Out of Trend” reported for analysis results as per the approved procedures.
• Implementing Quality Assurance systems effectively including handling of QMS activities in in the R&D.
• Actively participating in laboratory investigations and incidents ensuring GLP/GDP compliance.
• Handling of Excursions observed with Environmental monitoring, water system monitoring.
• Handling of temperature / RH excursions in the stability chambers / refrigerators / incubators.
• Review of Technical documents prior to QA approval (SOPs, Stability protocols / reports, URS, Qualification protocols, Qualification Reports, Out of Calibration report, Calibration delay reports, Instruments under maintenance reports)
• Review of Audit trail checklist as per approved procedures.
• Ensure all the instruments are qualified & calibrated and complying to CSV requirements.
• Collate and review data to be used in reports, investigations, key performance indicators (KPIs) and other quality indicating metrics.

• A bachelor's degree in Pharmaceutical Sciences, Analytical Chemistry or related field of study from an accredited institution. (Master's degree in the above fields of study preferred)
• Strong knowledge and experience with analytical laboratory activities in areas such as active pharmaceutical ingredients (API), drug products, analytical development, Quality Control (QC), Good Laboratory Practices (GLP)/Good Manufacturing Practices (GMP).
• A minimum of 3-5 years of relevant work experience in a pharmaceutical manufacturing company within the Quality function.
• Must possess strong documentation and technical writing skills, and be able to apply relevant scientific principles and practices.
• Must be proficient in computer skills and software applications such as Microsoft Office tools and Quality applications and software programs.
• Well versed knowledge of Quality Assurance principles required.
• Knowledge on the following will be added advantage
• Knowledge of Microbiology Laboratory activities.
• Knowledge on Manufacturing process (Sterile & Non-Sterile dosage forms).
• Experience of using statistical software.

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