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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,
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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. 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.
Le Coordinator Packaging aura pour mission d’assurer le flux des matières nécessaires pour le packaging ainsi que les activités de base de conditionnement des produits du site de Boudry (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.
Duties/Responsibilities
* 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.
* Être capable de travailler sur une ligne de conditionnement automatisée
* Être 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.
* Revue des dossiers de production.
* Être le point de contact principal pour le suivi des urgences
* Commandes de lots pour le packaging.
* Être le point de contact principal avec le service logistique pour l’approvisionnement des lots.
* Réception et contrôle des matières pour le packaging.
* Maintien et gestion des kanbans pour le packaging.
* Transactions informatiques ainsi que consommations lors de lots technique.
* Support pour les différentes lignes de packaging.
* Remplacement des opérateurs en cas d’absences sur les lignes packaging.
Qualifications
* Avoir une formation initiale de niveau CFC et une expérience de 3 ans dans le domaine de l’industrie pharmaceutique ou équivalente.
* Connaître l’environnement BPF/GMP
* Avoir une parfaite maîtrise du français.
* Être organisé et rigoureux, avec de bonnes capacités pour un travail d’équipe. Être proactif et polyvalent
If 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 Careers
With 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 Protocol
BMS 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 role:
Site-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.
Supporting People with Disabilities
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.
Candidate Rights
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/
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1603033 : Coordinator Packaging Operations
Location & Eligibility
Where is the job
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Location terms not specified
Listing Details
- Posted
- June 5, 2026
- First seen
- June 5, 2026
- Last seen
- June 5, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 51%
- Scored at
- June 5, 2026
Signal breakdown
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External application · ~5 min on bms's site
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