Assistant Manager Quality Control - Genetics Pharmaceuticals (Pvt.) Ltd. - Sundar Industrial State Raiwind Road, Lahore
(2020-07)
- To prepare testing plan and daily working schedule for the team.
- To review the plans for Analytical Method Validation/Verification, Stability testing plans, Annual training plans and Training need analysis.
- To perform analytical method validation of all existing or re-formulated products.
- To perform Analytical method validation and prepare the AMV protocols and reports.
- To review all the stability, AMV and reports prepared by the team.
- To prepare the and updated SOPs related to AMV and any other related SOP given by the Manager QC.
- To prepare the SOP of all QC instruments.
- To perform Performance Qualification of all QC Instruments.
- Handling and managing the OOS, OOT, CAPA, deviation and incident.
- Performing any special task related to the technical skills other than routine work asked by reporting authorities.
- To verify the log books of QC instruments and incoming sample of RM, IP FP, packing and stability.
- To Prepare of Standard testing method of Raw material and finish product.
- To perform the testing of raw material (Active pharmaceuticals and Excipients).
- To perform the Qualification, Handling and storage of Reference and working standards.
- To perform the testing of impurities in raw material and product.
- To perform the residual solvent on GC-Head Space.
- To perform the CDP and their documentation.
- To communicate with other departments regarding regulatory and dossier matters.
- To communicate with respective vendors against any services of QC Instruments.
- To perform the testing of lab chemicals.
- To maintain the consumable record of QC lab.
- To perform the Qualification of pharmaceutical water.
- To maintain the Preventive maintenance plan of QC instruments.
Senior Quality control Analyst - Unison Chemical Worker (Pvt.) Ltd. - Araian, 15 km Raiwind Road, Lahore
(2019-04 - 2020-07)
- To perform the analysis of Raw material, in process and finish product.
- Responsible to monitoring of daily instrument functional checks to ensure instruments are in optimal working conditions and verify due calibration and preventive maintenance.
- Observing and complying with Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP).
- Maintain accurate documentation of validation, qualification and calibration activities.
- Handling of troubleshoot and resolve issues related to operation of Laboratory instruments.
Assistant Quality control Analyst - Medipak pharmaceuticals Ltd. - Quaid-e-Azam Industria Estate Kot Lakhpat Lahore
(2017-03 - 2020-05)
- Perform the testing of IV solution, Irrigation solution and dialysis solution on IP and FP stage.
- Prepare reports of IV solution irrigation solution and dialysis solution.
- Perform analysis of active Pharmaceutical Ingredients. Perform analysis of excipients.
- To prepare the Volumetric solution, buffer and indicator solution for titration.
- To prepare the standardization Solution for titration.
- Testing of WFI, RO, and raw water samples to monitor the water quality on daily basis.
- To perform the sterility test if IV solution.
- To perform the LAL test of IV solution.
