Shriraj Kamat

Shriraj kamat

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location of Shriraj KamatHyderabad, Télangana, Inde
Followers of Shriraj Kamat1000 followers
  • Timeline

  • About me

    MS&T Specialist Novartis | Ex Teva | Ex Sanofi

  • Education

    • Bhatikar model hs, goa board

      -
      Ssc 85%
    • Kle university, karnataka-india

      2015 - 2017
      Master's degree pharmaceutics 70%
    • Kle university karnataka india

      2011 - 2015
      Bachelor of pharmacy 68%
    • Shree damodar hsss, goa board

      2009 - 2011
      Hssc 59%
  • Experience

    • Sanofi

      May 2017 - Aug 2020

      • Planning, Execution, Monitoring of Daily Activities, Documentation Filling and Reviewing, In-process Quality Checks of Tablets and Granules.• Ensuring Optimum Utilization of Capacity and Implement Process Excellence and Projects.• Train Operators / Subordinates to Ensure Quality, Safety Compliances and LEAN Work Procedures in the Department.• Assisting Validation activities, New product transfers, Equipment Qualifications, Preparation and Review of Validation Protocols and Reports.• Change control and Deviation Management.• Preparation and Review of SOP's, Equipment Risk Assessments and Process Risk Assessment Documents.• Daily monitoring of the Shift Output, Operational Equipment Efficiency(OEE) and Product Cycle Time.• Shop Floor Safety Officer. Show less

      • Production Executive

        Feb 2018 - Aug 2020
      • Quality Assurance Intern

        May 2017 - Feb 2018
    • Teva pharmaceuticals

      Aug 2020 - Aug 2023
      Technology transfer associate

      Responsible for Technology Transfer of Site Products and Developmental projects.Monitoring of Pre-Exhibit batches, Exhibit, Placebo, Validation Batches.Review of Technical Documents from Donor Site, Preparation of Protocols, Reports, GAP Analysis, APR's.Co-ordination with Formulation Team and Production for Execution of Batches.

    • Novartis

      Aug 2023 - now
      Ms&t specialist

      • Support validation program for Novartis Radio Ligand Therapy sites and Small Molecules sites including process validation, Ongoing Process Verification (OPV) and Risk assessment.• Create validation documentation including Annual/Quarterly OPV reports, Risk assessment, monitoring (OPV) plans based on alignment with Site Validation Leads.• Using monitoring tools such as CUSUM, OPV MONITOR, Minitab & Discoverant, perform OPV evaluations, control plots, assess process performance and provide insight, recommendation, and conclusion to the site MS&T Lead/Product Steward.• Create and review GxP documents including SOPs, working procedures, trend reports and technical investigations, as and when needed.• Provide active support during internal and external audits by collecting and presenting the requested process/ data and reports.• Coordinate & manage project for a smooth knowledge transfer activity from site/ function to corporate Center.• Act as single point of contact for the services delivered to sites/ functions by the respective team, including the review of feedback and timely completion of identified actions.• Coordinates with Global MS&T team, IT, QC/QA and regulatory CMC team for the ongoing data management, evaluation and reporting in the Monitoring tool. Show less

  • Licenses & Certifications

    • Fda approved expert staff in tablet manufacturing section

      Food & drugs administration goa
    • Investigator certification

      Novartis rlt indianapolis
      Jan 2025
    • Registered pharmacist

      Goa state pharmacy council
      Jan 2015
    • Statistical process control certification

      Indian statistical institute, pune chapter
      Jan 2025
    • Ielts academic grade: 7.5

      Cambridge assessment english exams cadiz
      Jan 2022