Quality Control Analyst / Analyste du contrôle qualité

Position Summary

Le/la L’analyste du contrôle de la qualité prépare les échantillons avec précision, effectue les analyses, consigne et évalue les résultats, et veille au respect des bonnes pratiques de fabrication (BPF) ainsi que des normes de qualité, tout en travaillant sous la supervision du superviseur du laboratoire de contrôle de la qualité.

The Quality Control Laboratory Analyst accurately prepares samples, conducts analyses, records and evaluates results, and ensures compliance with GMP and quality standards while working under the guidance of the Quality Control Laboratory Supervisor.

Responsibilities

  • Effectuer des tests de contrôle de la qualité sur des produits neufs, retournés et en inventaire à l’aide de pharmacopées approuvées et de méthodes d’essai internes
  • Préparer les échantillons, les étalons et les réactifs; réaliser des analyses humides et sèches; et évaluer et interpréter les résultats d’essais
  • Utiliser et assurer l’entretien des instruments analytiques (p. ex. FT‑IR, UV‑Visible, GC‑FID, HPLC, pH, conductivité)
  • Documenter, transcrire et tenir à jour avec exactitude les dossiers de laboratoire et les résultats d’analyses conformément aux exigences des BPF
  • Veiller au respect des BPF, des BPL et des procédures du système qualité, y compris l’étalonnage des équipements et les essais sur les matériaux
  • Surveiller les fournitures du laboratoire et soutenir les activités d’entretien des équipements
  • Maintenir un environnement de travail propre et sécuritaire et respecter les politiques en matière de santé, de sécurité et d’environnement
  • Soutenir la gestion des stocks, participer aux formations et aux réunions, et aider aux projets spéciaux selon les besoins
  • Perform quality control testing on new, returned, and in‑stock products using approved pharmacopoeia and internal test methods
  • Prepare samples, standards, and reagents; conduct wet and dry analyses; and evaluate and interpret test results
  • Operate and maintain analytical instrumentation (e.g., FT‑IR, UV‑Vis, GC‑FID, HPLC, pH, conductivity)
  • Accurately document, transcribe, and maintain laboratory records and test results in compliance with GMP requirements
  • Ensure adherence to GMP, GLP, and quality system procedures, including equipment calibration and material testing
  • Monitor laboratory supplies and support equipment maintenance activities
  • Maintain a clean, safe working environment and follow health, safety, and environmental policies
  • Support inventory management, participate in training and meetings, and assist with special projects as assigned

Required Experience & Knowledge

  • Diplôme d’études postsecondaires (minimum: CÉGEP) ou certificat dans un domaine scientifique connexe (p.ex.: Techniques de laboratoire – chimie analytique, chimie, biochimie ou domaine connexe)
  • Être membre de l'Ordre des chimistes est préféré.
  • Solides compétences analytiques et capacité à effectuer des tests de contrôle de la qualité précis, rigoureux et axés sur les détails dans un environnement où les délais sont serrés
  • Souci du détail démontré et capacité à maintenir une documentation et des dossiers exacts et complets
  • Excellentes habiletés de communication, tant à l’écrit qu’à l’oral
  • Connaissance pratique des bonnes pratiques de fabrication (BPF) et des exigences des systèmes qualité dans un environnement de laboratoire ou réglementé
  • Post‑secondary diploma (minimum CEGEP) or certificate in a science‑related discipline (e.g., Laboratory Technology – Analytical Chemistry, Chemistry, Biochemistry or related field)
  • Being a member of the Order of Chemists is preferred.
  • Strong analytical skills with the ability to perform accurate, detail‑oriented quality control testing in a time‑sensitive environment
  • Demonstrated attention to detail and ability to maintain accurate documentation and records
  • Effective written and verbal communication skills
  • Working knowledge of Good Manufacturing Practices (GMP) and quality system requirements within a laboratory or regulated environment
Actylis is an Equal Opportunity Employer. Actylis US does not discriminate on the basis of race, religion, color, sex, gender identity or expression, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided based on qualifications, merit, and business need.
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