if you want to work:

in one of the most modern biotechnology
centres in Europe
in place where profesionals
from all over the world work
on the highest-quality equipoment
in the production
of biotechnological
drugs, which dive access
to effective therapy to
more patients
in a company that will dive you stable employment competetive remuneration attracive benefits and the opportunity to participate in training at home and abroad
Currently we’re looking for
Downstream Process Development Specialist

Join “start-up” Biologics division with strong international and local team at site!


We are waiting just for you!



  • Downstream process development, optimization, characterization, and technology transfer
  • Planning and execution of laboratory scale studies for development and optimization of protein purification steps, including chromatography, filtration and membrane separations
  • Document observations, analyzing data, reporting results and conclusions for each experimental study
  • Trouble shooting activities and deviation assessment
  • Assessing improvement in DSP setup
  • Optimization of the process with regards of technical as well economic aspects
  • Evaluation of external suppliers of resins, filter membranes, disposable materials etc.
  • Supporting GMP manufacturing through process investigations and during process transfer
  • Design and execution of experiments based on DoE approach
  • Collaboration with USP, Analytical and Pilot Plant departments in order to achieve optimal results


  • MS or PhD in Biotechnology or related disciplines
  • 2+ years of experience in purification process development (preferably antibodies) in industry is highly desirable, however the candidates with strong experience and demonstrated track record in development and optimization of protein purifications in academia will also be considered. Experience with TFF and normal-flow filtration is a plus
  • A strong understanding of protein chromatography
  • Proven ability to work independently in hands-on laboratory setting
  • Experience in handling of lab scale chromatography systems is required. Experience with filtration units is a plus
  • Analytical skills with knowledge of electrophoresis (1D/2D) and spectrophotometric methods is desired
  • Experience writing technical development or scientific reports/publications
  • Basic knowledge of GMP standards is a plus
  • Good knowledge of spoken and written English