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Open nowPosted 58 days ago

Schaal

EURES job mobility portal314,718 open roles

Where
Arnhem/Nijmegen, Netherlands
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Your applicationOpen nowSchaalEURES job mobility portal · Arnhem/Nijmegen, Netherlands
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  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on EURES job mobility portal's own form.

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The clock on this job

Early applications get read.

7.8% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 1.7%1 day
  2. 3.5%3 days
  3. 7.8%7 days
  4. 14.6%14 days
  5. 34.1%30 days
This job: posted 58 days ago

The posting

- - Werken bij Radboudumc Productielaborant Radboud Translational Medicine B.V. - Schaal 6/7 - Bepaalde tijd - €2.771 - €4.182 - Sluit op 16-10-2026 - 1 jaar met uitzicht op verlenging - Laboratorium - 36 uur Productielaborant Radboud Translational Medicine B.V. - Schaal 6/7 - 1 jaar met uitzicht op verlenging - Bepaalde tijd - Laboratorium - €2.771 - €4.182 - 36 uur - Sluit op 16-10-2026 Jouw functie Als productielaborant bij Radboud Translational Medicine B.V. ben je een belangrijke schakel in de productie van radiofarmaca die ziekenhuizen en onderzoeksinstituten in zowel Nederland als het buitenland van levensbelang kunnen zijn. Jij weet als geen ander hoe belangrijk jouw werk is en je draagt jouw ervaring en kennis over aan jouw collega's. Jij zorgt voor structuur, enthousiasme en een extra dosis energie binnen ons team, vooral in de nachtdiensten. Je hebt niet alleen oog voor de details, maar weet ook het grote geheel in de gaten te houden. Je bent verantwoordelijk voor de productie van radiofarmaca en het onderhouden van de productielijnen. Daarnaast werk je mee aan het opstellen van nieuwe productiedocumenten, kwaliteitsverbetering en procesoptimalisatie. Werkzaamheden: - Produceren van radiofarmaca in een cleanroom volgens strikte protocollen. - Uitvoeren van de eerste batch review ten behoeve van de Qualified Person (QP). - Werken volgens de 'Good Manufacturing Practices' (GMP) en de stralingsveiligheidsvoorschriften. - Signaleren van afwijkingen en out-of-trends. - Bedienen van het cyclotron en uitvoeren van routinematige verrichtingen. - Mede voorbereiden en begeleiden van periodiek onderhoud. - Meewerken aan de ontwikkeling van nieuwe radiofarmaca. - Voorstellen doen voor procesverbetering en productoptimalisatie. - Bijdragen aan de ontwikkeling van interne kwaliteitssystemen. - Ondersteunen bij de afhandeling van deviaties en CAPA's. - Aanleveren van data voor management r...

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