Cigdem Sahin

Analytical Chemist at Cambrex Karlskoga AB
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Contact Information
us****@****om
(386) 825-5501
Location
Tallinn Metropolitan Area, EE
Languages
  • Türkçe Native or bilingual proficiency
  • ingilizce Native or bilingual proficiency
  • Fransızca Limited working proficiency

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Credentials

  • EURACHEM2019
    Eurachem 2019
    May, 2019
    - Oct, 2024
  • Environmental Management Systems( Çevre Yönetim Sistemleri)
    Türk Akreditasyon Kurumu (TÜRKAK) Turkish Accreditation Agency (TURKAK)
    Jun, 2013
    - Oct, 2024
  • ISO 9001 kalite yönetim sistemleri
    Türk Akreditasyon Kurumu (TÜRKAK) Turkish Accreditation Agency (TURKAK)
    Jun, 2013
    - Oct, 2024
  • Occupational Health and Safety Managemet Systems(OHSAS 18001:2007)
    Türk Akreditasyon Kurumu (TÜRKAK) Turkish Accreditation Agency (TURKAK)
    Jun, 2013
    - Oct, 2024
  • ISO 17025:2005 Laboratuvar yönetim sistemleri
    Esenek Consulting and Training Ltd.
    May, 2013
    - Oct, 2024
  • Ielts
    IDP Education Ltd
    Jan, 2019
    - Oct, 2024

Experience

  • Cambrex Karlskoga AB
    • Sweden
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Analytical Chemist
      • May 2023 - Present

  • The J. Molner Company
    • Estonia
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Senior Research Scientist
      • Sep 2021 - May 2023

  • Institut des Sciences Analytiques (ISA) - UMR 5280
    • France
    • Chemical Manufacturing
    • 1 - 100 Employee
    • Research Intern
      • Sep 2020 - Apr 2021

      • Separation of cross-linked GAGs using Liquid Chromatography-Mass Spectrometry technniques (Collaborated project with Allergan Inc.) • Separation of cross-linked GAGs using Liquid Chromatography-Mass Spectrometry technniques (Collaborated project with Allergan Inc.)

  • Kajaani University of Applied Sciences (KAMK)
    • Finland
    • Education Administration Programs
    • 100 - 200 Employee
    • Project Intern
      • Jun 2019 - Aug 2019

      • Method development for nutrient adsorption from wastewater by modified and foamed metakaolin geopolymer. • Designing of a 3-D printed column with modified metakaolin • Method development for nutrient adsorption from wastewater by modified and foamed metakaolin geopolymer. • Designing of a 3-D printed column with modified metakaolin

  • WORLD MEDICINE TÜRKİYE
    • Türkiye
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Research And Development Analyst
      • May 2017 - Aug 2018

      • Liquid chromatography-UV/RI/FL detection, method development for new formulated drugs • LC-UV, GC-FID method validation • Assay and impurity analysis for short and long term stability products • In-vitro characterization by dissolution testing for bioavailability information of orally taken drugs • Liquid chromatography-UV/RI/FL detection, method development for new formulated drugs • LC-UV, GC-FID method validation • Assay and impurity analysis for short and long term stability products • In-vitro characterization by dissolution testing for bioavailability information of orally taken drugs

  • DEVA Holding A.Ş.
    • Türkiye
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Stability Control Analyst
      • Sep 2013 - May 2017

      Cephalosphorine and penicillin quality control department • Assay and impurity analysis of end –product medicine for market release by using High Performance Liquid Chromatography • Residue aanalysis of ethanol in pharmaceutical end-products by using Gas Chromatography • Drug bioavailability testing by dissolution technique coupled with UV-Vis.- Spectrometer and HPLC-UV techniques Non-Steril Quality Control Department •Stability analysis of end-products according to SOP (in-house) based on ICH, FDA and EU guidelines Oncology Quality Control Department • Analysing stability products according to stability SOP, GMP and FDA guidelines. • In addition to these procedures, daily work includes: pH and conductivity analyses, assay analysis by UV-Vis spectorscopy, HPLC, GC, FTIR techniqued, measuring solid- liquid particle size, and humidity. Dissolution and gastro-resistance analyses, impurity analysis by HPLC, UPLC,,Thin layer chromatography techniques, potentiometrical titration. Show less

  • Recordati
    • Italy
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Summer Intern
      • Jul 2012 - Aug 2012

      Operating fundamental analytical techniques for end-product pharmaceuticals in terms of cGMP and GLP Operating fundamental analytical techniques for end-product pharmaceuticals in terms of cGMP and GLP

Education

  • Université Claude Bernard Lyon 1
    Master of Science, Analytical Chemistry
    2019 - 2021
  • University of Tartu
    Master of Science, Analytical Chemistry
    2018 - 2021
  • Anadolu University
    Bachelor of Applied Science (B.Sc.), Chemistry
    2008 - 2013
  • Wroclaw University of Technology
    Bachelor of Applied Science (B.A.Sc.), Medicinal and Pharmaceutical Chemistry
    2011 - 2012

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