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

Bristol Myers Squibb

Geprüftes Unternehmen

Boudry, Schweiz

vor 1 Woche

Geschrieben von:

Lena Schneider

beBee Recruiter

Beschreibung

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.

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.

Uniquely Interesting Work, Life-changing Careers

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 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