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Specialist Stability Studies (farma)

  • Location:

    Leiden, Netherlands

  • Contact:

    Nicol Heijtbrink

  • Job type:


  • Contact phone:

    +31 (0)20 406 9750

  • Industry:

    Biotechnology, Pharmaceutical

  • Contact email:

Are you an experienced professional with a strong background in the coordination of Stability Studies, this may be the position for you!

Job description

Our client is a leading, specialized pharmaceutical company. They are currently looking for a specialist to coordinate stability studies for their portfolio of 50-100 specialized products (diagnostics, subdermal and sublingual pharmaceuticals). In this position you play a leading and crucial role in the setup and execution of stability studies. You have a high level of responsibility and work an interdisciplinary team (QA, QC, RA & Development).  


  • Coordination GMP stability studies of the product portfolio;
  • Leading interdisciplinary stability meetings;
  • Responsible for compliance & quality of procedures;
  • Implementation of new assays;
  • Trend overview & analysis;
  • responsible for writing deviations, change control , CAPAs, continuous improvement.


  • BSc, MSc or Phd in analytical chemistry, biochemistry, biotechnology, pharmacy or similar;
  • >5 years of experience in a pharmaceutical environment (GMP);
  • Preferably exposure to stability studies;
  • Fluency in English (written and Orally is a must (Dutch is an advantage);
  • Highly organized and have demonstrable experience in coordinating tasks;
  • Able to prioritize, with an analytical and flexible mindset;
  • You are a driving force and work well within a team and together with other departments.


  • Contract: Permanent position, start with a 1 years contract;
  • Salary: €3000 -€4800 gross monthly;
  • Hours: Full-time, 32h discussable;
  • Region: Leiden.