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Validation Internship
Validation Internship-May 2024
Boudry
May 7, 2025
ABOUT BRISTOL MYERS SQUIBB
Bristol Myers Squibb is dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases.
10,000+ employees
Biotechnology, Healthcare
VIEW COMPANY PROFILE >>
About Validation Internship

  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.

  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 .

  Validation Internship 2024 – 6 mois

  Sujet de stage:

  Analyse de risques - Définition de la stratégie d’évaluation de la criticité des équipements GMP du site.

  Description : Dans leur environnement d'utilisation ou de fonctionnement en routine les équipements /systèmes sont exposés à des risques de défaillance même après qualification/validation. La défaillance peut avoir des impacts sur la qualité, le respect de la réglementation, la production, le personnel et l'environnement.

  L’objectif est de garantir le maintien du statut qualifié/validé des équipements/systèmes tout au long de leur cycle de vie. L'idée est de mettre en place un outil permettant de maitriser les risques de défaillance avec une stratégie solide qui définirait les vérifications et contrôles efficaces et applicables aux différents équipements GMP du site.

  Le résultat de cet exercice devrait établir un rationnel qui permettrait de:

  statuer sur la nécessité de requalification ou pas,

  définir la fréquence de requalification des équipements concernés .

  Activités annexes:

  Rédaction de templates de protocole/rapport de qualification pour différents types d'équipement,

  Qualification/Requalification: Support lors des exécutions et revue des documents de qualifications.

  Profil recherché:

  Formation : Ingénieur en Biologie, Biochimie, Qualité ou équivalent

  Outils : Microsoft

  Forte qualité relationnelle, aisance rédactionnelle, organisé, esprit d'analyse, autonome, dynamique, rigueur et force de proposition

  Langues : Français, Anglais (bon niveau)

  Connaissances : BPF/GMP, méthodes d’analyse de risques

  Date de démarrage prévisionnelle: 4 Mars 2024

  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 an inclusive culture, promoting diversity 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

  Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

  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 [email protected] . Visit careers.bms.com/ (https://careers.bms.com/eeo-accessibility) 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.

  Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

  Company: Bristol Myers Squibb

  Req Number: R1577753

  Updated: 2024-01-18 16:03:50.227 UTC

  Location: Boudry,Switzerland

  Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law.

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