Candidature facile
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Fonctions
Secteur
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Ville
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Le triPertinence
Jobs populaires
- IT
- Science
- Validation
- Production
- Protocole
- Biochimie
- Agent/e d'entretien
- Analyste business
- Analyste de développement
- Business Project Manager
- Chef/fe d'installation informatique
- Chef/fe de réalisation
- Ingénieur/e
- Ingénieur/euse en qualification
- Ingénieur/euse en validation en production
Temps de trajet
Méthode de candidature
Langue du job
Compétences
Fonctions
Secteur
Région
Ville
Expérience
Type de contrat
Régime de travail
Jobs populaires
- IT
- Science
- Validation
- Production
- Protocole
- Biochimie
- Agent/e d'entretien
- Analyste business
- Analyste de développement
- Business Project Manager
- Chef/fe d'installation informatique
- Chef/fe de réalisation
- Ingénieur/e
- Ingénieur/euse en qualification
- Ingénieur/euse en validation en production
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Knowledge of regulatory matters and Good Manufacturing Practices (GMP).
Knowledge of regulatory matters and Good Manufacturing Practices (GMP).
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Candidature facile
Proven experience as an independent validation project leader in the pharmaceutical industry, preferably GMP GLP.
Proven experience as an independent validation project leader in the pharmaceutical industry, preferably GMP GLP.
Candidature facile
Good understanding of the regulatory QC requirements (GMP, FDA)
Good understanding of the regulatory QC requirements (GMP, FDA)
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Vacature GMP-productie verantwoordelijke ATMP's (head of production) UZ LEUVEN in Leuven
Vacature GMP-productie verantwoordelijke ATMP's (head of production) UZ LEUVEN in Leuven
UZ Leuven
Leuven, België
Verleg grenzen als GMP-productie verantwoordelijke ATMP's n. Het produceren van geneesmiddelen zoals ATMPs gebeurt onder de Good Manufacturing Procedures (GMP). Omdat ATMPs anders zijn dan reguliere geneesmiddelen is er een GMP speciaal voor ATMPs. * Je staat mee in voor het plannen en organiseren van de GMP-producties, inclusief voorraadbeheer. * Je levert een actieve participatie bij (inter)nationale werkgroepen op het gebied van ATMP's; GMP en GMP-productontwikkeling en productie in het algemeen. * Je bent verantwoordelijk voor het uitbouwen, implementeren en onderhouden van het farmaceutisch kwaliteitssysteem voor de ATMP faciliteit (ATMP-QMS) en GMP in het algemeen binnen UZ Leuven (GMP-QMS) met betrekking tot ATMP productie vera
Verleg grenzen als GMP-productie verantwoordelijke ATMP's n. Het produceren van geneesmiddelen zoals ATMPs gebeurt onder de Good Manufacturing Procedures (GMP). Omdat ATMPs anders zijn dan reguliere geneesmiddelen is er een GMP speciaal voor ATMPs. * Je staat mee in voor het plannen en organiseren van de GMP-producties, inclusief voorraadbeheer. * Je levert een actieve participatie bij (inter)nationale werkgroepen op het gebied van ATMP's; GMP en GMP-productontwikkeling en productie in het algemeen. * Je bent verantwoordelijk voor het uitbouwen, implementeren en onderhouden van het farmaceutisch kwaliteitssysteem voor de ATMP faciliteit (ATMP-QMS) en GMP in het algemeen binnen UZ Leuven (GMP-QMS) met betrekking tot ATMP productie vera
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Bonne des exigences réglementaires associées (GMP
Bonne des exigences réglementaires associées (GMP
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Vacature Cleaning Validatie Engineer Heist op den berg; Select Projects
Vacature Cleaning Validatie Engineer Heist op den berg; Select Projects
Select Projects BVBA
Heist-op-den-Berg, België
Hierbij speel je een sleutelrol inewaken en verbeteren van cleaningprocessenhet b, zodat de productielijnen te allen tijde voldoenstrengste kwaliteitsnormen (GMP)aan de . * technical writing en GMP-regelgeving.
Hierbij speel je een sleutelrol inewaken en verbeteren van cleaningprocessenhet b, zodat de productielijnen te allen tijde voldoenstrengste kwaliteitsnormen (GMP)aan de . * technical writing en GMP-regelgeving.
Nous avons étendu votre recherche avec 2 offres d'emploi dans d'autres régions
A good knowledge of GLP/GMP rules is a plus.
A good knowledge of GLP/GMP rules is a plus.
Identify and list in a DVA (Data Vulnerability Assessment) the GMP/GDP data (raw data and metadata) involved in the
Identify and list in a DVA (Data Vulnerability Assessment) the GMP/GDP data (raw data and metadata) involved in the
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