Suraj Jumde

Suraj Jumde

Trainee production officer

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  • Timeline

  • About me

    Asst Manager at Intas Pharmaceutical, Ahmedabad

  • Education

    • Govt. Poly. Arvi

      2005 - 2007
      Diploma Chemical engg.
    • Savitribai Phule Pune University

      2009 - 2011
      CHEMICAL ENGINEERING Chemical Engineering
  • Experience

    • Sun Pharma Ind. Ltd.

      Sept 2011 - Aug 2012
      Trainee production officer
    • Inventys Research Company Pvt Ltd

      Nov 2012 - Jun 2015
      Jr. Production officer

      Responsible for daily production activities. To handle the Cynation, Esterification , Hydrolysis reaction. And also experience of DCS from where reaction parameters were handled.

    • Shilpa Medicare ltd

      Aug 2015 - Aug 2016
      Process Engineer

      Worked in API manufacturing Oncology products.

    • Wockhardt Pharma Limited.

      Aug 2016 - Jan 2020
      Jr. Executive
    • MJ Biopharma pvt. Ltd. Pune

      Jan 2020 - Jun 2021
      Executive production ( Bio similars)

      currently working in Biotech industry, handling the operation in Downstrem process. Experience in yeast and Ecoli insulin, glargine manufacturing using DEAE and Q chromatography column. (Cation & Anion Exchanger)

    • Intas Pharmaceuticals

      Jul 2021 - now
      Assistant Manager

      Handled green field project. Batch planning and execution. Experience in new project to set up plasma fractionation facility, area qualification and equipment qualification. Experience in FAT(virtual and offline), IQ, OQ, PQ execution and documentation. URS preparation and co ordination with vendor. Experience in computer system validation IQ, OQ for hardware and software of PLC/SCADA system. Verification and execution of FDS.Hand on experience in SAP. Knowledge of PO preparation, Batch confirmation in SAP.Experience in Ecoli insulin, glargine, manufacturing in downstream processing. Handling chromatography column of different size from 0.8 m to 2 m diameter.knowledge of automated buffer skid system. column packing unpacking. Different type of centrifuge like continuous and batch centrifuge. Knowledge of QMS activities like Deviation, change control, OOS,OOT. Process validation and cleaning validation protocol preparation. To carry out performance verification of equipment.SOP preparation and BPCR/BMR preparation. Show less

  • Licenses & Certifications