Operator 1, Packaging Operations
Vor 2 Tagen
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.
L’Operator I Packaging Operations aura pour mission d’assurer les activités de conditionnement des produits (blister, bouteille, étui, wallet, inspection visuelle), dans le respect de la réglementation BPF / cGMPs, des règles d’hygiène, et de sécurité. Il devra se conformer aux procédures définies par le système qualité du site pharmaceutique.
**Qualifications/connaissances exigées**
- Avoir une formation initiale de niveau CFC et une expérience de 5 ans dans le domaine de l’industrie pharmaceutique ou équivalente.
- Connaître l’environnement BPF/GMP et/ou l’environnement de travail en salle blanche.
- Avoir une parfaite maîtrise du français.
- Etre organisé et rigoureux, avec d’excellentes capacités pour un travail d’équipe.
- Avoir de bonnes connaissances de base de l’outils informatiques.
**Fonctions et responsabilités**
- Réaliser des opérations de conditionnement de base liées à la mise en bouteille, mise en blister, mise en étui, mise en wallet et / ou l’inspection visuelle suivant son curriculum de formation et selon les procédures en vigueur du système qualité.
- Maîtriser et effectuer le nettoyage des équipements liés à ces différentes étapes.
- Effectuer le vide de ligne, le nettoyage des pièces, des équipements et des salles après production.
- Etre capable de travailler sur une ligne de conditionnement automatisée
- Etre capable de travailler sur plus d’une ligne de conditionnement
- Se conformer aux objectifs de production et au respect du planning établi.
- Assurer la réalisation des opérations de conditionnement des lots industriels en environnement GMP et travailler de façon autonome et efficace selon les consignes de son responsable.
- Réaliser les changements de format et réglages de base définis dans les procédures.
- Contrôler, enregistrer et compléter les documents de travail pré-établis pour assurer un suivi des opérations réalisées (dossiers de lots remplis selon les GMP).
- Se conformer aux règles de sécurité et de sûreté 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 HSE / EHS.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
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