Job Description

Depanner et resoudre les problemes techniques ou operationnels lies aux matieres premieres, aux equipements et aux procedes. Collaborer avec les equipes de validation, nettoyage, maintenance, assurance qualite et autres fonctions transversales. Proposer, mettre en oeuvre et assurer le suivi des CAPA et des modifications de procedes. Rediger et reviser les PON, deviations et dossiers maitres de lots. Reviser et approuver les protocoles et rapports de validation ainsi que la documentation de transfert technologique. Soutenir l'introduction de nouveaux produits, les transferts de procedes et les initiatives d'amelioration continue. Mener des analyses de causes fondamentales et mettre en place des mesures preventives pour reduire les deviations et non-conformites. Identifier des opportunites pour optimiser les flux de travail, reduire les pertes et ameliorer l'excellence operationnelle grace aux pratiques Lean et Six Sigma. Promouvoir les meilleures pratiques et assurer la standardisation des procedes de fabrication.

Qualifications

Baccalaureat en chimie, en genie chimique ou dans un domaine connexe. Minimum de 3 ans d'experience dans un role similaire;

experience en industrie pharmaceutique exigee

. Excellente connaissance des BPF, des procedes de fabrication et de la redaction technique. Bilingue (francais/anglais). Competences demontrees en resolution de problemes, travail d'equipe et forte orientation vers l'amelioration continue. Maitrise de MS Office; une certification ou experience Lean Six Sigma constitue un atout.

Continuous Improvement Specialist

Troubleshoot and resolve technical/operational issues related to raw materials, equipment, and processes. Collaborate with validation, cleaning, maintenance, QA, and other cross-functional teams. Propose, implement, and follow up on CAPAs and process modifications. Draft and review SOPs, deviations, and master batch records. Review and approve validation protocols, reports, and technology transfer documentation. Support new product introductions, process transfers, and continuous improvement initiatives. Lead root cause analyses and implement preventive measures to reduce deviations and non-conformities. Identify opportunities to streamline workflows, reduce waste, and enhance operational excellence through Lean and Six Sigma practices. Promote best practices and drive standardization across manufacturing processes.

Qualifications

Bachelor's degree in Chemistry, Chemical Engineering, or related field. 3+ years of experience in a similar role;

pharmaceutical experience is required

. Strong knowledge of GMP, manufacturing processes, and technical writing. Bilingual (English/French). Proven problem-solving skills, team-oriented, and strong commitment to continuous improvement. Proficiency in MS Office; Lean Six Sigma certification or experience is an asset.
Job Type: Full-time

Work Location: In person