Sr Manager, Project Manager Supply Chain Cell - 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.

This role is part of the Global Cell Therapy Operations organization.

We aim to create a trusted cell therapy experience and excellence in commercialization with a world class CAR-T supply chain.

Our foundation is a culture where people can thrive.

The Sr Manager, Project Manager Cell therapy Supply Chain is accountable to drive and coordinate cross-functional deliverables as part of for European CAR-T product launches, and life cycle management events and projects.

In this the role holder must ensure the timely tracking and delivery of launch readiness tasks and support or drive improvement projects in the growing European Supply Chain Network.

Interact and communicate effectively with the global project teams and key stakeholders (manufacturing sites, quality, commercial, external supply, logistics) to keep the projects at track.

Effective issue identification, escalation and management.

The position is working cross-functionally with the global technical commercialization team, commercial operations.
QA/QP's, patient operations, IT and other internal stakeholders.

This role is based in Boudry, Switzerland and may require up to 20% of travel within Europe.

Responsibilities will include, but are not limited to the following:

Implement and coordinate technical launch processes as well as specific workstreams for CAR-T launch projects Europe.
Create detailed project plans and keep track of all activities related to launching and commercialization in order to meet key deliverables
Plan, schedule and manage effectively meetings with clear agendas and subsequent meeting minutes.
Support with presentations. Establish agenda, content, collation of materials, coordination of prereads and preparation/communication of followup actions.
Monitor and measure deliverables, team progress, ensure all actions are well identified, executed, followup with regional project lead and provide recommendations for improvement
Coordinate the Drumbeat in partnership with the Regional Project Launch Lead as well as crossfunctionally, in order to drive launch readiness and execution.
Effectively communicate with the technical commercialization teams and commercial operations as well as other internal stakeholders, escalate in time gaps and risks and manage effective resolution
Provide clear road map for timing of key activities and meetings
Ensure sustainability in growth postlaunch by establishing and tracking dashboards

Skill and Knowledge Requirements:

Ability to rapidly solve problems and deal with organizational complexity
At least 5 years' experience in planning and coordination of crossfunctional tasks in a pharmaceutical environment, experience in supply chain, expertise in other areas (e.g. commercial, marketing, finance) is a strong plus
Degree in Project management, Supply Chain, Business Management, Engineering
Medical, scientific and clinical knowledge
Excellent project management skills, structured work approach and strong analytical skills, ability to summarize and communicate at all levels of the organization
Experience with project work as a project manager
Experience with complex decision and planning processes
Change management experience.
Required written and verbal fluency in English language, other languages are a plus
Ability to prioritize and complete work with sense of urgency based on criticality
Knowledge of applicable regulations and standards
High attention to detail skills
High organization skills with ability to multitask several tasks in parallel

Preferred but not required:

Experience working in Apheresis, Cellular Therapy or Stem Cell Transplant programs
Experience in Life Cycle Management, Operational Excellence Qualification

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 will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.