Associate Scientist Upstream processing

Challenging position for experienced candidates with experience in mammalian cell culture

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What will your job be

We are looking for a motivated Associated Scientist within the field of upstream process development.

  • Under limited supervision, but as part of a team you will plan, prepare and execute scientific studies.
  • This will be part of a project plan, and you will be responsible for analyzing the results and reporting main conclusions.
  • Experiments may be performed in bioreactors or in a reduced-scale model.

What are we looking for

For the position of Associate Scientist Upstream processing we are looking for Master of PDEng candidate in a relevant discipline in biopharmaceutical sciences/engineering, biotechnology or virology

  • You have a M.Sc./PDeng in a relevant discipline, or a B.Sc with 3 years of experience in biotechnology or pharmacy.
  • You have a strong affinity with upstream process development, as demonstrated by experience with mammalian cell culture, hands-on experience with bioreactors, preferably at different scales / sizes.
  • Experience with production, technology transfer and knowledge of GMP is an advantage.
  • You are a motivated team player who is flexible and has a can-do attitude, and a pro-active mindset.
  • You are a team player with excellent communication skills.

What do we offer

  • Secondment via CheckMark Labrecruitment
  • Fulltime position, 40 hours/week
  • After your training period, your will occasionally be expected to work during weekend hours.

Where will you work

A global biotech company that focuses on the development, pro­duction and marketing of vaccines, recombinant proteins and antibodies to prevent and combat infectious and other diseases.
The USP department is responsible for the development of scalable, pharmaceutical-grade production 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 production 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. Within the department, a lab team is responsible for performing all hands-on experimental activities, data processing and documentation, whereas a team of scientists is responsible for the overall scientific approach and progress within our projects.

More information

Esther Moerdijk
0182 590 215
Na Rae de Jong
0182 590 216 6066

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