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Sunil Kamboj, Ph.D

Sunil Kamboj, Ph.D

SRF

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location of Sunil Kamboj, Ph.DWhitby, Ontario, Canada

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  • Timeline

  • About me

    Formulation Development Scientist |Ex. Dr. Reddys|Ex. Fresenius kabi

  • Education

    • Punjabi University

      2010 - 2012
      Master’s Degree Pharmaceutics

      Development of Solid SMEDDS formulation of poorly water soluble drugs

    • Punjabi University

      2012 - 2017
      Doctor of Philosophy (Ph.D.) Pharmaceutical Sciences

      Formulation Research and Development

    • Punjabi University

      2006 - 2010
      Bachelor’s Degree Pharmacy

      Activities and Societies: Art of living, Swiming

  • Experience

    • Department of Pharmaceutical Sciences and Drug Research

      Nov 2012 - Jul 2015
      SRF

      • To conduct Literature review, prior art experiment design of the product identified for development• Involved in patent circumvention, search of prior art, state of art and use of it in experimentation work• Conducting and performing, Pre-formulation profiling and formulation development• Use of Design of experimentation (DoE) and able to work on DoE software Design Expert® by Stat-Ease• Conducting and performing HPLC, FTIR, Rheology, Spray drying

    • Punjabi University

      Jan 2016 - Nov 2016
      Junior Research Fellow

      • To conduct Literature review• Conducting and performing, Pre-formulation profiling and formulation development• Use of Design of experimentation (DoE) and able to work on DoE software Design Expert® by Stat-Ease• Conducting and performing HPLC, FTIR, Rheology, Spray drying• Animal Handling, In Vivo experiments - drug distribution, Pharmacokinetic analysis

    • Fresenius Kabi Oncology Limited. - India

      Nov 2016 - Nov 2017
      Senior Research Scientist

      • Implementation of “QbD” approaches like identification of Quality Target Product Profile (QTPP), Critical Process Parameters (CPP), Critical Quality Attributes (CQA) and Technical Risk Assessment (TRA) using Failure Mode and Effects Analysis (FMEA), etc. • Implementation of DoE for screening and optimization of CPP and define control strategy for confirmatory and commercial production batches.• Planning and execution of lab trials• Pre-formulation studies of APIs which includes physico-chemical characterization, drug-excipient compatibility studies etc.• Reverse engineering of RLDs• Prototype formulation development• Preparation and review of stability protocols.• Experience in RMG granulation, Roller compaction, Compression and film coating of tablets• Understanding of regulatory requirements.• Scale Up and Technology Transfer• Actively participated in troubleshooting for all issues affecting formulation development and analytical procedures within the team for faster movement of projects• Para IV fillings • NCE-1 product development Show less

    • Dr. Reddy's Laboratories

      Dec 2017 - Jun 2022

      • Specialist FRD

        Dec 2019 - Jun 2022

      • Scientist

        Dec 2017 - Dec 2019

    • Biolab Sanus Farmacêutica

      Jun 2022 - Jan 2023
      Formulation Scientist

    • Pharmascience

      Jan 2023 - Jan 2025
      Senior Research Scientist

    • Thermo Fisher Scientific

      Jan 2025 - now
      Technical Project Leader

  • Licenses & Certifications