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Manager, Master Planning - Boudry, Schweiz - Bristol Myers Squibb
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.
In this position the Manager, Master Planning will manage within a mid and long- term scope the logistics activities for the manufacturing site of Boudry and be part of the projects core team (internal or global scope) until the shipping of the goods out of the site.
This position will be lead in close collaboration with key users working within supply management department and other internal stakeholders (Quality Control, Quality Assurance, Validation, Maintenance, Production, Global Supply Chain Planning, Global MDM...).
you will act as backup for his/her peer and can deputize his/her manager
• Define and guarantee the execution of the Manufacturing Resources Planning in the mid-term and long plans in a timely and smooth manner (inclusive availability of materials, resources, ERP set-ups)
• Be accountable for the timely release of SKUs, coordinate release prioritization if required
• Lead capacity in the 18/24 months windows in close coordination with the different stakeholders (Quality Assurance, Quality Control, Validation, Maintenance, Production, Warehouse, Supply Chain...)
• Key contact for the Global Planning Supply Team and market planners, coordinate customer services activities
• Be in charge of the Manufacturing KPI and supply metrics
• Act as Supply SME point of contact for New Molecules Introduction Project. Coordinate technical lot and validation lots execution within the Supply Team (MDM, components availability, scheduling)
• Accountable for global supply initiatives (act as change agent, contribute to project core-team decision)
• In charge of responsible for CCR tasks completion and/or verification within Supply Management Department. Perform CCR (Change Control Request) impact assessment when required.
• Act as ERP super-user for scheduling activities
• Follow-up and define solutions for issues or deviations related to his/her scope of activities
• Propose process improvements ideas and guide them to realization, actively participate in continuous improvement initiatives (LEAN)
• Responsible any creation/update of controlled documents related to his/her scope of activities (SOP, WP, LIST, etc.)
:
• + 5/10 years' experience in the field of production or supply chain planning
• Experience in an industrial international environment, in pharmaceutical area an asset
• Familiar with project management tools soft skills
• Capability to work in a changing environment and beyond pre-defined processes and to actively map workflow, define and implement new way of working
• Pro-active personality with an eye for anticipation and continuous improvement
• Conscientious, reliable in action follow-up
• Analytical skills, team-player and natural leadership
• Good negotiation, priority management communication (works in transparency), problem solving and decision-making skills
• Excellent IT proficiency: MS Office, Excel ++, ERP (SAP +++), Oracle experience is an asset
• Fluency both in French and English
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through scienceTM ", 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
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
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 . Visit 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.
