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 .
Position Summary
L'Operator Bulk Operations aura pour mission d'assurer les activites de fabrication des produits (capsules et (ou) comprimes), dans le respect de la reglementation BPF / GMPs (Bonnes Pratiques de Fabrication / Good manufacturing practice), des regles d'hygiene, et de securite. Il devra se conformer aux procedures definies par le systeme qualite du site pharmaceutique.
Realiser des operations de production tel que la pesee des matieres, la
preparation des melanges de poudre ainsi que la conduite de lignes
visuelle automatisee...) suivant son curriculum de formation et selon les procedures en vigueur du systeme qualite.
Duties/Responsibilities
Maitriser et effectuer le nettoyage des equipements lies a ces differentes
etapes.
Effectuer le vide de ligne, le nettoyage des pieces, des equipements et des salles apres production.
Effectuer les changements de format sur les equipements.
Effectuer les controles physiques elementaire des produits fabriques.
Se conformer aux objectifs de production et au respect du planning etabli.
Assurer la realisation des operations de fabrication des lots industriels en
environnement GMP et travailler de facon autonome et efficace selon les
consignes de son responsable.
Participer aux transferts de nouveaux produits, a la validation des procedes industriels, a la fabrication des lots de validation et a la qualification des
equipements.
Controler, enregistrer et completer les documents de travail preetablis pour assurer un suivi des operations realisees (dossiers de lots remplis selon les GMP).
Se conformer aux regles de securite et de surete du site pharmaceutique.
Annoncer les situations dangereuses, les presqu'accidents/incidents et les accidents qui pourraient survenir sur le site aupres de son responsable
direct et aupres du departement EHS (Environment, Health & Safety).
Qualifications
Avoir une formation initiale de niveau CFC et une experience de 5 ans dans le
domaine de l'industrie pharmaceutique ou equivalente.
Connaitre l'environnement BPF / GMP.
Avoir une parfaite maitrise du francais.
Etre organise et rigoureux, et avoir des qualites relationnelles pour un travail
d'equipe.
Avoir de bonnes connaissances de base de l'outil informatique. (Word, Excel,
Power point, Outlook)
Location Boudry
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(TM) , 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.
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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