Sr Manager, Cell Therapy Launches & Lifecycle, Europe > Boudry > Joboolo FR :
Société : Bristol Myers Squibb Lieu : Boudry Canton of Neuchâtel
Working with Us Challenging.
Meaningful.
Life-changing.
Those aren’t words that are usually associated with a job.
But working at BristolMyersSquibb is anything but usual.
Here, uniquely interesting work happens every day, in every department.
From optimizing a production line to the latest breakthroughs in celltherapy, 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.
BristolMyersSquibb 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.
This role is part of the Global CellTherapy Operations organization.
We aim to create a trusted celltherapy 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, CT launches & lifecycle EU 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 launches , support or drive improvement projects as well as manage product lifecycle events 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 launches and product lifecycle 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 pre-reads and preparation/communication of follow-up actions.
Be responsible for opening and managing project change controls in BMS quality system Monitor and measure deliverables, team progress, ensure all actions are well identified, executed, follow-up with regional project lead and provide recommendations for improvement Coordinate the Drumbeat in partnership with the Regional Project Launch Lead as well as cross-functionally, in order to drive launch readiness and execution.
Support other launch leads and project teams with operational tasks where needed 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 post-launch by establishing and tracking dashboards Skill and Knowledge Requirements:
Ability to rapidly solve problems and deal with organizational complexity and the unknown At least 5 years’ experience in planning and coordination of cross-functional projects 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 using MS project &/or Smartsheet tools 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 multi-task 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 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 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.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. BristolMyersSquibb BoudryCanton of Neuchâtel
