Sohail Anwer Email and Phone Number

 As per Academia Teaching:Taught of various disciplines of pharmaceutics and quality management at under graduate and post graduate level including:• Quality Management • Six sigma• Forensic Pharmacy• Physical Pharmacy• Bio pharmaceutics & Pharmacokinetics• Bio statistics• Pharmaceutical Management and Marketing Curriculum development:• Reshaped a pharmaceutical quality management course of pharm. D by innovatingteaching to adjoin concept of basic quality tools, root cause analysis and process improvement as prerequisite of pharmaceutical industry • Designed a teaching course for the M.Phil program titled as Quality Operation in order to strengthen the needs of pharmaceutical industry , which is self exercise of quality by design process analytical technique process capability , lean management and six sigma Administrative activities: In addition to teaching and research, involved in various administrative activities: • Acting HOD , Pharmaceutics • Admission process • Conduct and monitor over all examination process as Central superintendent• Proceedings of board of studies and board of faculty • Preparation of CIEC/ HEC/ PCP visits• QEC activities at faculty level • Technical Adviser to Director, for the budget/ purchase and procurement • Faculty Focal Person for Plagiarism test and similarity index Technical Support:• Establish Quality management lab. as per Pharma curriculum • Plan and organize Industrial visits for under graduate students• Team member for bio medical accreditation program at FEST • I.Q,O.Q and P.Q of Hitachi based HPLC system with Chromeleon software Event Management:• Organize and facilitate workshop on Basics of HPLC for Pharm.D students• Organize and facilitate workshop on Introduction of LAL test • Organize and facilitate sports week from 2006 to 2012

Major Job activities according to Industrial Experience: • Preparation of Job description of Assistant Managers , Seniors and Juniors analysts • Management and Monitoring of overall Analytical activities of Raw materials, Finished goods and Microbiological testing and their trouble shootings • Establishment of Lab. SOP’s. with reference to G.Q.S• Preparation of documentation for calibration , specifications and analytical methods • Preparation of documentation for I.Q , O.Q and P. Q of instruments and manufacturing equipments.• Periodic internal and G.Q.S audits of Q.C and Micro lab. • Stability studies of existing products • Management of reference standards and reference samples Quality Assurance Supervision:• Quality Assurance liaisons for planning, checks, control and implementations• Monitoring of overall in- process control at semi finished and finished stages• Monitoring of overall sampling activities of Raw materials, Finishing goods • SOP’s establishment of the systems, checks and control with reference to G.Q.S• Review of Batch deviation’s , Reconciliation, Reprocessing and Reworks • Deployment of strategies & execution to prevent Failure investigation • Approval of Change control proposal as initiate by production and engineering.• Preparation of Process Validation protocols Manufacturing and Packaging records.• Handling of Market complaints. • Provide assistance to supply chain in order to maintain GMP within the factory and ware houses/ distribution Locations.• Explore ways and means for cost effective process and production management by evaluation of key performance indicator’s of overall technical operations.• Monitoring of EHS issues in order to ensure safeguards of all company’s assets.• Periodic cGMP audits of overall plant operations. • Periodic Suppliers audits in order to maintain inventory

• Management and Monitoring of overall Analytical activities of Raw materials, Finished goods and Microbiological testing and their trouble shootings• Performance and Documentation of system suitability and analytical validation. • Establishment of Lab. SOP’s. with reference to G.Q.S• Stability studies of existing products • Management of reference standards and reference samples• Preparation of documentation for calibration , specifications and analytical methods • Also have experience in product transfer technology and analytical product transfer

Manufacturing supervision of tableting and coating Area

Literature survey through chemical abstracting and research journals , Method validation , Clinical trials on pharmacokinetics

In-depth training in syrup manufacturing and packing area as well as inspection, testing of semi finished and finished products