Kotchawan Lertchairitthikun

Analytical Chemist at Cambrex Karlskoga AB
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Contact Information
us****@****om
(386) 825-5501
Location
Greater Stockholm Metropolitan Area, SE
Languages
  • ภาษาไทย -
  • English -

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Phumwit Phuimart

Kotchawan has many skills in the field of analytical chemistry, pharmaceutical chemistry and also knows about the pharmaceutical industry regulation, especially in common technical dossiers (CTD). She is very detail-oriented and honest person. Doing well in teamwork, and be the kindly colleague to me and the others.

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Credentials

  • Statistics Foundations: The Basics
    LinkedIn
    Apr, 2021
    - Oct, 2024
  • Certification of biological product registration Module 2 : Quality control and quality assurance
    National Vaccine Institute (Po)
  • Certification of biological product registration Module 3 : Non-clinical trial
    National Vaccine Institute (Po)
  • edX Verified Certificate for Making Biologic Medicines for Patients: The Principles of Biopharmaceutical Manufacturing
    edX
  • edX Verified Certificate for Medicinal Chemistry: The Molecular Basis of Drug Discovery
    edX

Experience

  • Cambrex Karlskoga AB
    • Sweden
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Analytical Chemist
      • Jan 2022 - Present

      An Analytical chemist in a new product stability and release testing group. - Test Identify, Assay, Related substances of intermediate and APIs using HPLC, UPLC, IR, GC - Review test results and report deviation - Control function control of the instruments - Train GMP work to other teams - Perform Inter laboratory precision An Analytical chemist in a new product stability and release testing group. - Test Identify, Assay, Related substances of intermediate and APIs using HPLC, UPLC, IR, GC - Review test results and report deviation - Control function control of the instruments - Train GMP work to other teams - Perform Inter laboratory precision

  • Uppsala University
    • Sweden
    • Higher Education
    • 700 & Above Employee
    • Research Assistant
      • Jul 2021 - Sep 2021

      Quantitative metabolomics study in biological samples using LC-MS/MS.

    • Masters Student
      • Aug 2020 - Jul 2021

      Excellence in Analytical Chemistry- Quantitative metabolomics using LC-MS/MS “Validation and Application of Targeted Metabolomic Profiling by using a Biocrates MxP® Quant 500 Kit”

  • University of Tartu
    • Estonia
    • Higher Education
    • 700 & Above Employee
    • Graduate Student
      • Sep 2019 - Aug 2021

      Excellence in Analytical Chemistry - Metrology - Method validation - Analytical method development Excellence in Analytical Chemistry - Metrology - Method validation - Analytical method development

  • The University of Tartu Art Museum
    • Tartu, Tartumaa, Estonia
    • Research Assistant
      • Jul 2020 - Aug 2020

      - Do IR database. - Do IR database.

  • Medica Innova Co. Ltd.
    • 1 - 100 Employee
    • Pharmacist
      • Apr 2017 - Aug 2019

      - Review and evaluate Common Technical Dossier (CTD document) for drug registration - Set up validation method for pharmaceutical products (compendial and non-compendial method) - Write stability protocol, review the result and report the final information - Improve a method for dissolution profile to test pharmaceutical equivalence before bioequivalence study - Develop protocol and prepare documents for the bioequivalence study’s report (Quality part) - Create and revise Standard Operating Procedure (SOP) and Working Instruction (WI) to comply with ISO17025 Show less

  • The Government Pharmaceutical Organization
    • Bangkok, Bangkok City, Thailand
    • Pharmacist
      • Nov 2015 - Apr 2017

      - Coordinate with Research and development, Production, Quality control, Quality assurance and Engineer department for all activities involving in the influenza vaccine project - Support technical data and prepare vaccine policy documents which are done by the National Vaccine Institute - Collaborate with a production team to contribute vaccines for clinical trial study (phase III) - Respond to project leader meetings - Set up an academic seminar - Coordinate with Research and development, Production, Quality control, Quality assurance and Engineer department for all activities involving in the influenza vaccine project - Support technical data and prepare vaccine policy documents which are done by the National Vaccine Institute - Collaborate with a production team to contribute vaccines for clinical trial study (phase III) - Respond to project leader meetings - Set up an academic seminar

  • Siam Bioscience Co., Ltd.
    • Nakhon Pathom, Thailand
    • Research Assistant
      • Mar 2014 - Dec 2014

      Monoclonal antibody (mammalian-derived biosimilar) research group - Develop serum-free medium plate form for selecting high producer mammalian cells instead of the serum-containing medium in order to decrease time-consuming for host cell line development which is one of the upstream process development. Monoclonal antibody (mammalian-derived biosimilar) research group - Develop serum-free medium plate form for selecting high producer mammalian cells instead of the serum-containing medium in order to decrease time-consuming for host cell line development which is one of the upstream process development.

Education

  • Uppsala University
    Master of Science - MS, Analytical Chemistry
    2020 - 2021
  • University of Tartu
    Master of Science - MS, Excellence in Analytical Chemistry
    2019 - 2021
  • Mahidol University
    Doctor of Pharmacy (Pharm.D.), Industrial Pharmacy
    2009 - 2015

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