Patrick van den Heuvel

Pharmaceutical Development Analyst at Regivet BV
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Contact Information
us****@****om
(386) 825-5501
Location
Zwijndrecht, South Holland, Netherlands, NL
Languages
  • Engels Full professional proficiency
  • Duits Limited working proficiency
  • Spaans Elementary proficiency
  • Nederlands Native or bilingual proficiency
  • Russisch Elementary proficiency
Skills

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Bio

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Credentials

  • Farmaceutisch Technicus - Verpakken
    Edufarma
    Nov, 2020
    - Nov, 2024
  • Farmaceutisch Technicus - Steriele Toedieningsvormen
    Edufarma
    Nov, 2019
    - Nov, 2024
  • Scientific Report Writing
    NIOW Taal- en tekstexperts
    Jun, 2019
    - Nov, 2024
  • Farmaceutisch Technicus - Vloeibare en halfvaste toedieningsvormen
    EduFarma
    Apr, 2019
    - Nov, 2024
  • Farmaceutisch Technicus - Vaste toedieningsvormen
    EduFarma
    Nov, 2018
    - Nov, 2024
  • Farmaceutisch Technicus - Algemeen
    EduFarma
    Apr, 2018
    - Nov, 2024
  • Astronomy: Exploring Time and Space
    Coursera
    Mar, 2015
    - Nov, 2024
  • Circadian clocks: how rhythms structure life
    Coursera
    Mar, 2015
    - Nov, 2024
  • Terrorism and Counterterrorism: Comparing Theory and Practice
    Leiden University
  • The Addicted Brain
    Emory University

Experience

  • Regivet BV
    • Netherlands
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Pharmaceutical Development Analyst
      • Mar 2022 - Present

  • Solipharma
    • Oudenbosch, Noord-Brabant, Nederland
    • QC Specialist / QC Coördinator Projects
      • Dec 2020 - Feb 2022

      Coördination of projects for the introduction of pharmaceutical products into the portfolio of the company. The writing of validation and calibration protocols and reports, writing of SOP's. Analysis method development and optimization in a GMP environment. Analytical support for troubleshooting and development of products. Coördination of projects for the introduction of pharmaceutical products into the portfolio of the company. The writing of validation and calibration protocols and reports, writing of SOP's. Analysis method development and optimization in a GMP environment. Analytical support for troubleshooting and development of products.

  • Tiofarma
    • Oud-Beijerland
    • Development analyst
      • Aug 2017 - Dec 2020

      Analytical method development and validation for chemical and physical tests on tablets, capsules, granulates, creams, ointments, solutions, and suspensions in a GMP environment. Analytical support for drug product development. Writing validation, verification and transfer protocols and reports, SOPs and work instructions. Instrument specialist for HPLC and GC devices, consisting of trouble-shooting, maintenance and validation of the hardware. Analytical method development and validation for chemical and physical tests on tablets, capsules, granulates, creams, ointments, solutions, and suspensions in a GMP environment. Analytical support for drug product development. Writing validation, verification and transfer protocols and reports, SOPs and work instructions. Instrument specialist for HPLC and GC devices, consisting of trouble-shooting, maintenance and validation of the hardware.

  • Meeùs
    • Netherlands
    • Insurance
    • 100 - 200 Employee
    • Administratief medewerker
      • Jul 2016 - Jul 2017

  • Erasmus MC
    • Netherlands
    • Hospitals and Health Care
    • 700 & Above Employee
    • Intern
      • Nov 2014 - Aug 2015

  • GE Jenbacher Gas Engines
    • Alblasserdam, Netherlands
    • Helpdesk Employee
      • Feb 2009 - Feb 2015

  • HORNBACH Baumarkt AG
    • Germany
    • Retail
    • 700 & Above Employee
    • Sales Employee
      • Feb 2007 - Jul 2008

Education

  • Avans University of Applied Science
    Biomedical Laboratory Research
    2012 - 2015
  • Johan de Witt- gymnasium
    2002 - 2008

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