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Sujata Garud

Sujata Garud

Q C Chemist

Followers of Sujata Garud205 followers
location of Sujata GarudPune, Maharashtra, India

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  • Timeline

  • About me

    Sr. Executive at Sydler remedies pvt ltd at Bhosari

  • Education

    • Shivaji University, Kolhapur

      2000 - 2004
      Bachelor of Pharmacy - from satara college of pharmacy satara First Class

  • Experience

    • OKASA PHARMA PRIVATE LIMITED

      Sept 2004 - Feb 2009
      Q C Chemist

      Analyzed raw materials, inprocess and finished products. sampling of RM, IP and FP samples.Handled QC instruments like HPLC,GC, AAS, Dissolution test apparatus etc. Review of analytical data. Review of RM, FP specifications as per IP, BP, USP and Inhouse.

    • Murli Krishna Pharma Pvt. Ltd.

      Feb 2009 - Jul 2010
      Senior Officer

      Review the RM/FP specifications. Review all analytical data in QC lab as reviewer. Involved in QC analysis planning. Calibration of QC instructions like HPLC, GC, Autotitrator, Dissolution and UV spectrophotometer. Handling Gas chromatography instrument.

    • Emcure Pharma Limited Hinjwadi Pune

      Feb 2012 - Jun 2017
      Senior Research Fellow

      Preparation and revision of RM, FP specifications. Preparation and review of Analytical method validation/verification protocol and reports.Preparation and review of Analytical method transfer protocol and reports. Review of analytical data.

    • Sai Life Sciences Ltd

      Jun 2017 - Feb 2019
      Research Scientist

      Preparation and review of Raw materials and finished product specifications. Preparation and review of AMT protocol and AMT reports. Preparation and review of analytical method validation/verification protocol/reports. Preparation and revision of SOPs. Update the calibration schedule.

    • Agio Pharmaceuticals Ltd.

      Mar 2019 - Nov 2019
      Assistant Manager

      Worked as team leader in Quality Assurance for analytical documentation. Review the regulatory affairs documents and support to regulatory compliance. Responsible for handling of change control, out of specifications (OOS) , deviation, out of trend (OOT) results. Handling of market compliant. Responsible for release the batches.Responsible to review all analytical data. Review all QC instruments calibration record. Review all SOPs.

    • SYDLER REMEDIES PRIVATE LIMITED

      Mar 2024 - now
      Sr. Executive

      Analytical QA reviewer, Responsible for QMS functions like, change control, Deviation, CAPA, incidence. investigation of OOS results. Review of analytical data. Responsible for inline GDP, GLP in QC laboratory. Responsible for review of analytical documents which are submitted to RA dept.

  • Licenses & Certifications

    • FDA approval in chemical and instrumental analysis

      FDA Maharashtra
      May 2005