Muhammad Arshad

Experience

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  Helix Pharma

  Mar 2010 - Apr 2010

  Management Trainee Pharmacist

   Exposure to different preparation procedure of different dosage forms. Exposure to different documentation for the preparation of batches. Exposure to different laboratory instruments (dissolution apparatus, disintegration apparatus, spectrophotometer, friabiliator, and hardness tester).

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  Otsuka Pakistan Limited

  Apr 2010 - Oct 2016

  Quality Assurance Department Manufacturing process control studies Documentation of GMP deviation in production area Batch document Audit Inprocess check sheets preparation and review  training to fresh and new inprocess inspectorsQuality Control Department Records of laboratory testing maintenance including raw data, testing procedures and results. All drug products QC analytical section batch documents reviewed. A record of equipment maintenance and use of equipment logs. Assignment to QC unit of total responsibility for ensuring drug product concentrations fulfilling the label claims. Stability of products- protocols, schedules, and reports. Show less Quality Assurance Department Inspection of Production and warehouse area for GMP Compliance Sampling and testing of packaging materials Arrangement of packaging and F.G reference samples as per SOPs Inprocess Documentation  Approval of Line clearance for different processes. Reporting of different type of data like percent rejections, breakdowns, batch changing over, deviations etc.Quality Control Department Testing of inprocess control, finished goods and raw material  Sampling and testing of water samples from water treatment plant. Instruments uses- HPLC Based Amino Acid Analyzer Gradient System, HPLC ( isocratic) FT-IR (Fourier Transformation Infra Red Spectroscopy), AA (Atomic Absorption),, GC, Flame Photometer, UV-spectrophotometer, LPC (Liquid Particle Counter System), Polarimeter, .Oxygen Analyzer, TOC (Total Organic Carbon Analyzer) ), Karl Fischer Analyzer, Auto Titrator. Preparation of test solutions and standard solutions, and their standardization. Preparation of retrospective data of chemical analysis of different products. Show less

  • Executive Quality Assurance

    Jun 2014 - Oct 2016

  • Senior Quality Assurance Officer

    Apr 2010 - May 2014
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  Barrett Hodgson Private Limited

  Oct 2016 - now

  Executive Quality Contol and Assaurance

   Maintain record of routine and experimental drug products analysis. Stability testing record, schedules and protocols of commercial and experimental batches. Maintain the records of standardization for the reference standards of APIs. Necessary adjustments in the existing analytical methods. Literature survey for the development and implementation of new analytical methods. Drug products testing for APIs, preservatives and impurities, and interpretation of the results. Pharmaceutical quality control parameters testing of different dosage forms like classical and control release tablet, syrup, suspension, capsule, control release pellets, topical solution, topical ointment, topical jell, ophthalmic solutions, ophthalmic suspension, ophthalmic ointment, injection. infusion etc. Show less