Informations générales
Société / Etablissement
Seqens est un acteur mondial intégré de solutions pharmaceutiques et ingrédients de spécialité, disposant d'une large gamme de produits, de services et de technologies. Le Groupe propose à ses clients des services de fabrication à façon pour les marchés pharmaceutiques et de spécialités ainsi qu'un large portefeuille de principes actifs et d'intermédiaires pharmaceutiques.
Le groupe exploite 24 sites de production, 10 centres de R&D et emploie plus de 3 200 personnes principalement en Europe, Asie et Amérique du Nord. Plus de 300 scientifiques, ingénieurs et experts développent des solutions sur mesure pour nos clients et veillent à ce que les produits soient passés en production avec succès.
Référence
2025-1464
Description du poste
Famille / Sous-famille d'emploi
Quality & Regulatory - Quality Control
Type de contrat
Contrat à durée indéterminée
Intitulé du poste
Quality Control Sr Technician M/F
Contexte du poste :
We are seeking a dedicated Quality Control Sr Technician to join our team.
You will support the manufacture of API, functional polymers, and lipids by ensuring the on-time delivery of high-quality test results under cGMP guidelines.
Additionally, you will help improve operational efficiency by streamlining procedures and eliminating waste.
Principales missions :
• Plan, schedule, and execute QC activities, including testing raw materials, in-process samples, finished products, and stability samples under full cGMP guidelines.
• Conduct lab Out Of Specification (OOS), Out Of Tolerance (OOT), and material non-conformance investigations.
• Support the validation and transfer of analytical methods from the Analytical Development group to Quality Control operations.
• Troubleshoot, maintain, procure, and install various analytical instruments.
• Maintain the laboratory in compliance with the company’s cGMP and Environmental Health and Safety (EH&S) procedures.
Les atouts pour réussir :
• Minimum four years of analytical laboratory experience under GMP after obtaining a BSc/MSc in a chemistry-related major, preferably in analytical chemistry.
• Experience in current Good Manufacturing Practices (cGMP) in a Quality Control (QC) setting within the pharmaceutical industry, with working knowledge of analytical instruments such as GC, GC/MS, HPLC, LC/MS, Ion chromatography, and other wet chemistry skills.
• Proven ability to interact successfully with QA, and experience with writing/investigating LIR, QI, CAPA, and peer review.
• Strong communication skills and the ability to build strong interpersonal relationships with colleagues and customers.
Location : Devens Massachusetts, USA
Localisation du poste
Localisation du poste
Etats Unis, Massachusetts, Devens