Senior Quality Control Analyst

vor 1 Woche


Neuenburg, Schweiz CARESILIUM Vollzeit

CARESILIUM est une société de conseils en ingénierie 100% suisse romand. Notre flexibilité, ainsi que les valeurs que nous portons : l'honnêteté, la franchise et la simplicité, nous permettent de créer des accompagnements sur mesures qui tiennent comptes de tous les besoins, les enjeux et les contraintes de nos partenaires. Une collaboration de confiance, c'est avant tout un recrutement bienveillant et transparent.


Avec CARESILIUM, rejoignez une équipe où vos attentes professionnelles ET personnelles sont au centre des décisions. Chaque parcours est accompagné individuellement par un manager technique qui saura vous guider vers votre but.


Et rappelez-vous toujours : chez CARESILIUM, notre plus belle valeur, c'est vous.


Vous avez des questions ? Besoin de précision ? N'hésitez pas à prendre contact avec nous


Le Poste

Résumé du poste :

En tant que Consultant Senior QC Analyst, au sein d'une organisation CDMO, vous effectuerez une grande variété d'analyses chimiques ou biologiques sur des produits, des matériaux en cours de fabrication ou des échantillons en soutien au programme d'assurance et de contrôle de la qualité de l'entreprise. L'intégration se fera au cours des deux premières semaines. À partir du milieu de la deuxième semaine, et principalement à partir de la troisième semaine, vous devrez diriger seul votre propre plan d'essai.


Fonctions Essentielles

Dans ce rôle, une journée typique peut inclure, mais n'est pas limitée à, ce qui suit :

  • Effectuer des tests analytiques conformément aux spécifications relatives aux matières premières et à la mise sur le marché des produits (HPLC, GC, UV/VIS, IR, dissolution, pH, conductivité, TOC, titrage, pesage, expériences de chimie humide, etc.)
  • Examiner les données analytiques.
  • Assumer la responsabilité des activités de transfert et de validation des méthodes.

Exigences Du Poste

Ce poste pourrait vous convenir si :

  • Vous disposez d'une expérience actuelle d'au moins 5 ans en matière d'essais multifonctions dans les secteurs d'essais QC suivants : Chimie, AS&T, Microbiologie, Stabilité.
  • Vous avez une connaissance approfondie de l'HPLC/UPLC dans un environnement réglementé.
  • Vous avez démontré votre capacité à travailler de manière autonome.
  • Vous possédez de solides compétences en matière de dépannage et de résolution de problèmes.
  • Vous avez le souci du détail et d'excellentes compétences écrites et orales.
  • Vous possédez des valeurs éthiques et d'engagement profondes.
  • Vous parlez couramment l'anglais (C1) ; le français est un atout.
  • Vous avez une connaissance approfondie des procédures d'assurance et de contrôle de la qualité.

Profil

Expérience / Formation : Pour être considéré pour ce poste, vous devez être titulaire d'un BS/BA en sciences de la vie ou dans un domaine connexe. Vous avez au moins 5 ans d'expérience dans un laboratoire de contrôle qualité Pharma/Biotech/CDMO. HPLC/UPLC et Empower requis. Une expérience en SE-UPLC, en dosage de peptides et de glycanes est souhaitable.

Karrierestufe
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