Principal Scientist, Packaging - Boudry, Schweiz - Bristol Myers Squibb

Bristol Myers Squibb
Bristol Myers Squibb
Geprüftes Unternehmen
Boudry, Schweiz

vor 1 Woche

Lena Schneider

Geschrieben von:

Lena Schneider

beBee Recruiter


Beschreibung

Bei Bristol Myers Squibb lassen wir uns von einer einzigen Vision inspirieren - die Veränderung des Lebens von Patienten durch Wissenschaft.

In den Bereichen Onkologie, Hämatologie, Immunologie und Herz-Kreislauf-Erkrankungen - und eine der vielfältigsten und vielversprechendsten Pipelines der Branche - trägt jeder unserer leidenschaftlichen Kollegen zu Innovationen bei, die bedeutende Veränderungen vorantreiben.

Wir verleihen jeder Therapie, für die wir Pionierarbeit leisten, eine menschliche Note. Kommen Sie zu Bristol Myers Squibb und machen Sie einen Unterschied.


Position Summary

  • MS&T is a sciencedriven organization dedicated to building indepth and comprehensive knowledge of our products and their processes. We work across the entire lifecycle of our Pharmaceutical Products and across both internal and external manufacturing/packaging and API Manufacturing.
  • This position leads and/or manages global and strategic (or technically complex) projects for Bristol-Myers Squibb Global Commercial Supply and ensures projects are delivered within agreed timelines, cost, and quality targets.
  • Transfers product knowledge into the Global Commercial Supply organization.
  • Provides technical expertise and support to Packaging Operations to improve capacity, quality, cost or to establish root cause. The success of this function requires effective collaboration with Pharmaceutical Development, External
  • Manufacturing, Supply Chain, Manufacturing, Packaging Operations, Regulatory CMC, Quality Assurance and Analytical Science and Technology.

Duties/Responsibilities

  • Manage strategic packaging projects (such as the Technology Transfer of a product from Development) from project initiation to closure including after action reviews.
  • Advocate best practice project methodologies and tools. Develop, write, and review project documentation including project plans, test protocols, risk assessments and reports.
  • In collaboration with the Product Champion provide technical/scientific expertise and support to packaging sites.
  • In collaboration with the Technology Leader Packaging, support product, technology, or packaging improvements/changes.
  • Assist with writing and reviewing of CMC documentation associated with project or packaging changes.
  • Transfer reliable and well understood packaging processes into Global Supply or within the network. Transfer the knowledge from the sending unit to receiving unit and Product Steward. Ensure knowledge is captured and transferred.
  • Engage with Packaging sites/Development and CRO/CMO's and advocate the use of scientifically sound principles. Advise on the definition of CQA's and CPP's and an appropriate control strategy.
  • Participation in the design, execution and data analysis associated to technical trials/batches associated with the projects. Writing and reviewing project documentation including project plans, test protocols, risk assessments and reports.
  • Update a scientific knowledge base. Advises on Scientific and Business developments (including Technology, Processes, Regulations etc.).
  • Applies and advocates continuous improvement mindset.
  • Assist with the development of Standards, guidelines and SOPs to enhance the quality and robustness of our manufacturing operations, knowledge transfer and technical support processes.
  • Scouting for new technologies and new suppliers (technological survey).

Reporting Relationship - Director, Process and Technology (Boudry MS&T)

  • Minimum bachelor's degree in Packaging Engineering/Technology, Packaging Development, or similar education in this field.
  • 10 years of experience in the Pharmaceutical/Cosmetics/Food industry.
  • Knowledge and experience of primary, secondary, and tertiary packaging materials.
  • Good working knowledge of QA, cGMP, and the Pharmaceutical Regulatory framework
  • Good knowledge of various types pharmaceutical packaging processes/technologies.
  • Good knowledge of Technology Transfer and validation.
  • Demonstrated project leadership/management experience. Experience of multisite/crosssite project management.
  • Working knowledge Lean and 6 Sigma methodologies.
  • Good leadership skills and ability to influence and work across organizational boundaries.
  • Effective communication skills, good command of English and preferably another European language.
Wir setzen uns auf der ganzen Welt leidenschaftlich dafür ein, das Leben von Patienten mit schweren Krankheiten zu beeinflussen.

Unsere gemeinsamen Werte Leidenschaft, Innovation, Dringlichkeit, Verantwortlichkeit, Inklusion und Integrität befähigen uns, unsere individuellen Talente und unterschiedlichen Perspektiven in einer integrativen Kultur einzusetzen und bringen das höchste Potenzial jedes unserer Kollegen hervor.

Bristol Myers Squibb weiß um die Bedeutung von Balance und Flexibilität im Arbeitsumfeld. Wir bieten daher eine Vielzahl von attraktiven Benefits, Dienstleistungen und Programmen an, die unseren Mitarbeitern di

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