Monday, October 27, 2025
Bristol Myers Squibb

Operator Bulk Operations

Posted: 1 days ago

Job Description

Working with UsChallenging. 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. Take your career farther than you thought possible.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. Read more careers.bms.com/working-with-us .Position SummaryL'Operator Bulk Operations aura pour mission d'assurer les activités de fabrication des produits (capsules et (ou) comprimés), dans le respect de la réglementation BPF / GMPs (Bonnes Pratiques de Fabrication / Good manufacturing practice), des règles d'hygiène, et de sécurité. Il devra se conformer aux procédures définies par le système qualité du site pharmaceutique.Réaliser des opérations de production tel que la pesée des matières, lapréparation des mélanges de poudre ainsi que la conduite de lignesautomatisées (Encapsuleuse, Comprimeuse, Pelliculeuse, inspectionvisuelle automatisée...) suivant son curriculum de formation et selon les procédures en vigueur du système qualité.Duties/ResponsibilitiesMaîtriser et effectuer le nettoyage des équipements liés à ces différentesétapes.Effectuer le vide de ligne, le nettoyage des pièces, des équipements et des salles après production.Effectuer les changements de format sur les équipements.Effectuer les contrôles physiques élémentaire des produits fabriqués.Se conformer aux objectifs de production et au respect du planning établi.Assurer la réalisation des opérations de fabrication des lots industriels enenvironnement GMP et travailler de façon autonome et efficace selon lesconsignes de son responsable.Participer aux transferts de nouveaux produits, à la validation des procédés industriels, à la fabrication des lots de validation et à la qualification deséquipements.Contrôler, enregistrer et compléter les documents de travail préétablis pour assurer un suivi des opérations réalisées (dossiers de lots remplis selon les GMP).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 responsabledirect et auprès du département EHS (Environment, Health & Safety).QualificationsAvoir une formation initiale de niveau CFC et une expérience de 5 ans dans ledomaine de l'industrie pharmaceutique ou équivalente. Connaître l'environnement BPF / GMP. Avoir une parfaite maîtrise du français. Être organisé et rigoureux, et avoir des qualités relationnelles pour un travaild'équipe. Avoir de bonnes connaissances de base de l'outil informatique. (Word, Excel,Power point, Outlook)Location BoudryIf you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.Uniquely Interesting Work, Life-changing CareersWith a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.On-site ProtocolBMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your roleSite-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information https //careers.bms.com/california-residents/Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

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