Blank
Let's Get Started
Blank
Career Opportunities
Back to job search

Data Scientist / Engineer Process Development

Do you have a background in data science, bioinformatics and / or biotech? Would you like to be directly involved in the fight against the global
"Corona virus" (COVID-19) pandemic? Then keep reading!

Job description

The drug-substance development department at our client Janssen Vaccines & Prevention is responsible for the development of scalable, pharmaceutical-grade USP and DSP processes for viral vaccines using mammalian cell lines as a production platform. Novel technologies are used to make sure that the processes are safe, reliable, scalable and cost-effective, so that the vaccines can be produced in large quantities at low costs. The developed processes are transferred into GMP production facilities for the production of clinical batches and scaled-up for commercial production. All activities are performed in close collaboration with other departments.

We are looking for a motivated Associated Scientist within the field of Process development. With several of our projects moving into late stage, the need to support our studies by means of historical data analysis has increased. Furthermore, we need to increase data-integrity by performing additional reviews. You will be primary responsible for data verification and translating these data into reportable formats as well as historical data mining. You will also perform basic data analysis and statistics from which you will report the main conclusions. Finally, you will be involved in the development and improvement of data management systems. The results of your work will be directly used for regulatory submissions.

Responsibilities

  • You will be primary responsible for data verification and translating these data into reportable formats as well as historical data mining.
  • You will also perform basic data analysis and statistics from which you will report the main conclusions.
  • Finally, you will be involved in the development and improvement of data management systems.
  • The results of your work will be directly used for regulatory submissions.

Profile

  • MSc. in a relevant discipline in biopharmaceutical / biomedical sciences / engineering, biotechnology
  • Must have 1-3 years of experience in process development (lab/production/biotechnology)
  • Strong affinity with data management and data analysis.
  • Experience with production, technology transfer and knowledge of GMP is an advantage.
  • Programming skills and knowledge in Python, Visual Basic, R-shiny, or Spotfire are considered to be an important advantage

Benefits

  • Contract 1 year via Oxford Global Resources, realistic long term perspective
  • Salary indication: from €3100 to € 3800 gross a month based on education/experience
  • Holidays: 25 (+12)
  • Working hours: 40 hours per week
  • Location: Leiden

Reference nr: 15526