 Supervise and performs Analysis of Incoming Material including Raw Material (API/Excipients), In-Process, Finished and Stability samples according to Predefined procedures as per Pharmacopoeia Monographs and SOPs. Performing physical and wet chemistry testing on Raw Materials using a wide variety of techniques like; Titration, Loss on Drying, Karl Fischer, Melting point, limit test, Viscosity, Bulk/Tap density, Particle sieve analysis, pH/Conductivity Testing, TLC, Polarimeter… Show more  Supervise and performs Analysis of Incoming Material including Raw Material (API/Excipients), In-Process, Finished and Stability samples according to Predefined procedures as per Pharmacopoeia Monographs and SOPs. Performing physical and wet chemistry testing on Raw Materials using a wide variety of techniques like; Titration, Loss on Drying, Karl Fischer, Melting point, limit test, Viscosity, Bulk/Tap density, Particle sieve analysis, pH/Conductivity Testing, TLC, Polarimeter, Refractometer, Identification Tests. Performing Raw Materials testing using the Instrumentation like; HPLC, UV/VIS Spectrophotometer, FTIR Spectrophotometer, Residual Solvents by GC.  Analysis of in-process and Semi Finished products for Assay/Impurity, water content, Dissolution and physical testing like Friability, Disintegration, Hardness. Performing Chemical analysis of Purified water (Phase I, Phase II and Phase III) including various chemical testing and TOC by GE TOC analyser for various sampling points.  Performing sampling and testing of Incoming Packaging components like Bottles, Caps, Labels, Inserts, Base Films and Foils for various physical and chemical tests. Provide guidance and plan of action to the subordinates during QC analysis when production events occur as defined by SOP. Reviewing test records and reports, STM, SOPs, auditing system logs and instruments calibration records. Supervise QC officer to include; but not limited to overseeing testing, check progress of samples for release and ensure assigned task are performed on timely manner. Work distribution among QC officers based on priorities. Provide comprehensive formal and informal leadership to promote work environment and communicate overall business expectations to QC. Interact with other departments for testing information required for methods and or proper documentations. Monitoring stocks of reagents and Laboratory supplies. Train new employee on basic laboratory techniques Show less

Carrying out the Quality Control activities on Various Buffer Reagent and Solutions preparations related to Molecular technology/Biotechnology Research Projects.

Carrying out the research work on Protein & Enzymes Extraction, Isolation & purification and further characterization from various Camel Tissues and Blood and Study relevancy with Disease.

 Performing the QC analysis of Raw material, finished pharmaceutical product and In-house stability samples using European and US pharmacopoeia methods, with high level of meticulous attitude including interpreting and processing results. Performing physical and chemical testing on raw materials using a wide variety of techniques like; Titration, Loss on Drying, Karl Fischer moisture determination, Heavy metals limit test, UV/Vis Spectrophotometer & IR spectrophotometer. Performing… Show more  Performing the QC analysis of Raw material, finished pharmaceutical product and In-house stability samples using European and US pharmacopoeia methods, with high level of meticulous attitude including interpreting and processing results. Performing physical and chemical testing on raw materials using a wide variety of techniques like; Titration, Loss on Drying, Karl Fischer moisture determination, Heavy metals limit test, UV/Vis Spectrophotometer & IR spectrophotometer. Performing wet chemical analysis on Raw Materials like; limit test, pH, TLC, Identification, Total Ash, Viscosity, Bulk/Tapped density & Particle size.  Analysis of in-process and finished drug products for Dissolution, Assay/Impurity, Content uniformity, water content and residual solvent testing of drug intermediates and products. Analysis of tablets, capsules, lotions, creams and injectable for HPLC-Assay/Related compounds, Impurities and degradants/Content and Blend Uniformity for release and stability testing.  Performed USP dissolution basket & Paddle (I and II) for tablets and capsules coupled with UV-Vis and HPLC analysis. Show less

 Carrying out the In-process and final bulk product analysis of Vitamin B12 by HPLC for assay and impurities during scale-up developmental batches. Vis/Spectrophotometer for Cell mass determination for Pseudomonas Denitrificans at different stages of scale-up developmental batches. Carbohydrate analysis by using Skalar analytical Instrument during different stages of Vitamin B12 development batch and maintains sufficient carbohydrate level throughout the scale-up batch as a… Show more  Carrying out the In-process and final bulk product analysis of Vitamin B12 by HPLC for assay and impurities during scale-up developmental batches. Vis/Spectrophotometer for Cell mass determination for Pseudomonas Denitrificans at different stages of scale-up developmental batches. Carbohydrate analysis by using Skalar analytical Instrument during different stages of Vitamin B12 development batch and maintains sufficient carbohydrate level throughout the scale-up batch as a nutritional supplements.  Carrying out the In-process and final bulk product analysis of human Insulin by HPLC for assay and impurity during scale-up batches. Preparation of lab reagents, in-house and compendia reference standards, production medium for Vitamin B12 and human Insulin scale-up developmental trials. Inventory control of laboratory solid and liquid chemicals for use in the laboratory. Assisted in Carrying out Commissioning, Installation Qualification as well as Operational Qualification for New Brunswick Scientific (NBS) Reactors and Fomenters for the Production of Vitamin B12 and human Insulin. Preparation & review of SOPs, STPs, GTMs, Work Instructions and spreadsheet to obtain technical results. Assisted in Preparation of Batch Manufacturing Records (BMR) and other technical documents related to the production of Vitamin B12 and human Insulin; to Quality Control and Production departments. Carrying out communication, coordination and updating related to scale-up developmental issues with cross-functional department like Quality Control, Production department and Instrument maintenance department. Show less