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Open nowPosted 31 days ago

Qualified Person (QP

EURES job mobility portal63,496 open roles

Where
Arnhem/Nijmegen, Netherlands
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Your applicationOpen nowQualified Person (QPEURES job mobility portal · Arnhem/Nijmegen, Netherlands
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  4. 14.0%14 days
  5. 33.7%30 days
This job: posted 31 days ago

The posting

FAL Duiven B.V. Qualified Person (QP) 32-40 uur per week | Duiven | Intentie tot vast dienstverband Jouw handtekening maakt het verschil. Als Qualified Person bij Farmaceutisch Analytisch Laboratorium Duiven BV zorg jij ervoor dat kwaliteit niet alleen een belofte is, maar een aantoonbaar en betrouwbaar resultaat. Bij FAL Duiven BV produceren we generieke geneesmiddelen in tabletvorm. Ongeveer 45 collega's werken dagelijks vanuit verschillende afdelingen samen aan geneesmiddelen die voldoen aan hoge kwaliteitsstandaarden. FAL Duiven BV is onderdeel van Medochemie, een internationaal farmaceutisch concern met productielocaties in Cyprus, Nederland en Vietnam. Als jonge, dynamische en informele organisatie staan kwaliteit en slagvaardigheid bij ons centraal. Ben jij een ervaren GMP-professional die inhoudelijk scherp is, besluitvaardig is en graag samenwerkt? Dan biedt FAL Duiven BV jou de ruimte om zichtbaar bij te dragen aan de kwaliteit en veiligheid van geneesmiddelen. Jouw impact FAL Duiven BV maakt deel uit van Medochemie. Wij werken volgens hoge GMP-standaarden en beschikken over een MIA/fabricagevergunning en GMP-certificaat. Als QP ben jij de onafhankelijke kwaliteitsautoriteit binnen onze organisatie. Je beoordeelt en geeft grondstoffen, bulk tabletten en verpakte producten vrij. Daarmee heb je direct invloed op de kwaliteit, veiligheid en beschikbaarheid van geneesmiddelen voor patiënten. Je werkt dicht op de praktijk en bent een inhoudelijke sparringpartner en verbindende kracht tussen Quality, Regulatory Affairs, Quality Control en Operations (productie en logistiek). Dit ga jij doen - Certificeren en vrijgeven van grondstoffen, bulk tabletten en verpakte producten. - Beoordelen van batchdocumentatie en analyseresultaten. - Beoordelen van afwijkingen, OOS-resultaten, CAPA's, Changes en kwaliteitsrisico's. - Bewaken dat activiteiten plaatsvinden binnen GMP, de MIA/fabricagevergunning en het kwaliteitssysteem. -...

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