Technician Bulk Operations Osd-lslf
vor 2 Monaten
**Working with Us**
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Le Technician Bulk Operations aura pour mission d'assurer les activités de fabrication des produits essentiellement sous forme de comprimés, dans le respect de la réglementation BPF / GMPs, des règles d'hygiène, et de sécurité. Il devra se conformer aux procédures définies par le système qualité du site pharmaceutique.
**Duties/Responsibilities**
- Réaliser des opérations de production tel que la pesée des matières, la préparation des mélanges de poudre ainsi que la conduite de ligne automatisée dans les activités de fabrication de comprimés suivant son curriculum de formation et selon les procédures en vigueur du système qualité.
- Supporter techniquement les opérateurs dans les activités de production. Participer et supporter de manière active aux transferts de nouveaux produits, à la validation des procédés industriels, à la fabrication des lots de validation et à la qualification des équipements.
- Maitriser l'outil MES (Manufacturing Execution System) dans la gestion des dossiers de lot et des consommations associées.
- Maîtriser et effectuer le nettoyage des équipements du matériel et des salles liées aux différentes étapes de production.
- Effectuer les changements de format et le vide de ligne production.
- Mettre à jour et créer des documents techniques nécessaires au fonctionnement des équipements et de la ligne (instructions d'utilisation, de nettoyage).
- Se conformer aux directives et instructions définies dans le système qualité de notre site pharmaceutique.
- Assurer la réalisation des opérations de production des lots techniques, commerciaux et cliniques en environnement GMP et travailler de façon autonome et efficace selon les consignes de son responsable.
- Contrôler, enregistrer et compléter les documents de travail préétablis pour assurer un suivi des opérations réalisées (dossiers de lots remplis selon les BPF / GMP).
- Effectuer les contrôles physiques élémentaire des produits fabriqués.
- Se conformer aux objectifs de production notamment au respect du planning établi.
- Assurer le suivi jusqu'à la reprise de la production lors d'intervention de maintenance sur un équipement.
- Analyser les pannes d'équipements et être support à la maintenance en cas d'intervention.
- Réaliser les changements de formats et réglages de base définis dans les procédures.
- Être référent technique pour les opérateurs.
- Former les nouveaux collaborateurs et les opérateurs sur les différentes lignes de production et être le réfèrent de la formation (On the Job Qualified Trainer).
- Participer à l'amélioration continue en proposant des idées d'améliorations sur les lignes.
- Se conformer aux règles de sécurité et de sureté du site pharmaceutique.
- Annoncer les situations dangereuses, les presqu'accidents/incidents et les accidents qui pourraient survenir sur le site auprès de son responsable direct et auprès du département EHS (Environment, Health & Safety).
**Qualifications**
- Avoir une formation initiale de niveau CFC et une expérience de 5 ans dans la production pharmaceutique ou idéalement 3 ans comme technicien dans l'industrie Pharmaceutique.
- Connaître parfaitement l'environnement BPF / GMP, et avoir une bonne connaissance de l'industrie pharmaceutique, notamment dans les différents process de fabrication de forme solide tel que la compression de poudres, la granulation humide / sèche, le pelliculage.
- Avoir une parfaite maîtrise du français et des notions d'anglais (A2).
- Etre organisé et rigoureux, et avoir de grandes qualités relationnelles pour un travail d'équipe.
- Communiquer de façon claire avec les services support ainsi que les personnes responsables du développement des nouveaux produits.
- Avoir un esprit critique et est force de proposition dans un but d'amélioration continue (certification yellow belt).
- Savoir utiliser les outils informatiques (Word, Excel, Power point, Outlook) et de maitriser le fonctionnement d'un MES.
- Partager son savoir et former les nouveaux collaborateurs, opérateurs sur les différents équipements de la zone bulk.
**Uniquely Interesting Work, Life-changing Careers**
**On-site Protocol**
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design
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