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Open nowPosted 4 days ago

Analytical Scientist qPCR & ELISA | Pharma | Geel

EURES job mobility portal270,805 open roles

Where
Turnhout, Belgium
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Your applicationOpen nowAnalytical Scientist qPCR & ELISA | Pharma | GeelEURES job mobility portal · Turnhout, Belgium

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  4. 14.3%14 days
  5. 33.7%30 days
This job: posted 4 days ago

The posting

Jouw baan als Analytical Scientist qPCR & ELISA

Wil jij mee bouwen aan innovatieve biologische geneesmiddelen die wereldwijd patiënten helpen? Als Analytical Scientist qPCR & ELISA kom je terecht binnen het Analytical Science and Technology team van een toonaangevende farmaspeler in Geel. Je ondersteunt de ontwikkeling, validatie en transfer van analytische methodes die een cruciale rol spelen binnen productieprocessen van biologische geneesmiddelen. Daarbij werk je nauw samen met R&D, MSAT en Quality Control. Je combineert labo-expertise met data-analyse en wetenschappelijke rapportering binnen een sterk gereguleerde omgeving.

Gelukkig kunnen we op jou rekenen bij het:

  • Optreden als expert voor qPCR- en ELISA-methoden binnen MSAT.
  • Begeleiden van methodetransfers van R&D naar productie-ondersteunende teams.
  • Ondersteunen van transfers naar QC inclusief troubleshooting en documentatie.
  • Ontwikkelen, optimaliseren en valideren van analytische testmethoden.
  • Opzetten en uitvoeren van analytische studies en DOE-experimenten.
  • Uitvoeren van data trending en root cause analyses.
  • Opstellen van protocollen, rapporten en technische presentaties.

Je werkt graag zelfstandig en behoudt overzicht wanneer meerdere projecten tegelijk lopen. Dankzij je analytisch inzicht leg je snel verbanden tussen resultaten en mogelijke oorzaken. Je communiceert helder met verschillende stakeholders en vertaalt complexe gegevens naar duidelijke conclusies.

Hard skills

  • PhD in Biotechnologie, Biochemie of Life Sciences.
  • Minimaal 2 tot 5 jaar relevante ervaring binnen pharma of biotech.
  • Sterke expertise in qPCR en ELISA voor analytische toepassingen.
  • Ervaring met method development, qualification en validation onder cGMP.
  • Vlotte kennis van Nederlands en Engels, schriftelijk en mondeling.
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