Our client is committed to developing first-in-class or best-in-class vaccines for some of the world's most life-threatening infectious diseases. We have built a dedicated, world-class, multi-functional team across a variety of disciplines to develop a promising vaccines pipeline. In Leiden, we have a workforce of 700 scientists and support staff, 45% of our employees has a nationality other than Dutch with over 20 nationalities represented. We partner with many of the world's leading experts, academic and clinical institutions and other pharmaceutical companies for the development of vaccines against, for example, Ebola and HIV.
In our organization entrepreneurial people are working in a dynamic culture in which innovation and a 'can do' state of mind are the central points. In order to strengthen our team we are continuously looking for enthusiastic, talented people who have the ambition to develop themselves and can be of value to our client.
The drug-substance development (DSD) department 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.
- 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
What do we offer:
Contract via Kelly Services of period 40 hours per week, 3 months
Start date: ASAP
An international environment where you can learn a lot in challenging projects
When interested please react through the application process with your English resume.
About Kelly Services
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In keeping with the AWGB (Algemene Wet Gelijke Behandeling) Kelly Services welcomes applications from any and all eligible candidates regardless of ethnicity, gender, disability, religion, sexual orientation or age.