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.
This position manages manufacturing supply process of Boudry site, from the procurement of the raw materials to the shipment of finished goods (purchasing/replenishment and detailed scheduling ).
As a key player for the organization, this position will interact cross functionally either with the departments based in Boudry site like Project Management Office (PMO), Operations (Bulk, Packaging, Warehouse), Quality Control (QC), Technical Services, Quality Assurance (QA), Procurement, Launch Excellence, Manufacturing Sciences & Technology, and Finance or within the Pharma Supply Planning (GSP) organization.
The Senior Manager, Site Supply Management works in close collaboration and alignment with his/her peers based in Boudry and among the Pharma Supply Organization. He can act as the deputy of the Head of the Site Supply Chain.
Duties
Team management
- Manage and develop the Purchasing and Panning team for all activities in scope (short, mid-term horizon)
- Define the mid-term strategy with regards to activities/projects and resource planning (gap-assessment, succession plans),
- Define and set the strategic objectives and provide periodic reporting on overall activities as requested,
- Ensure pro-active priority and activity management for his/her team/activities,
- Communicate pro-actively, consistently and coordinate with the different stakeholders,
- Lead corrective actions and improvement initiatives,
- Ensure the Key Performance Indicators (KPI) of her/his activities are defined and met as per targets, including: write-off control, leadtime, timely delivery, RFT.
Operations:
- Accountable for timely supply of products and materials as per business requirements (Demand plan, Launches, Labelling changes, Projects, Safety stock, Shipment…) and for sufficient inventory for all raw materials,
- Manage change management and act as supply change owner
- Responsible for lead time optimization and monitoring,
- Supervise and lead the demand plan management from supply plan cycle to reaching OTIF target,
- Act as single point of contact for all operational interactions with GSP,
- Capacity review with the impacted plant departments (QA, QC, Bulk Operations, Packaging Operations and the Warehouse),
- Act as single point of contact for QA release priorities when applicable,
- Act as information coordination point for launches and labelling changes,
- Responsible for the write offs and to maintain the costs in line with the cost target defined.
Participates as a key-SME to projects in relation with supply activities:
- New product introduction projects
- Lean initiatives
- Launch and molecule transfer
- Product security
Compliance
Ensures all activities in scope or conducted in compliance with GMP.
This implies but is not limited to:
- Process definition, Standard Operating Procedures (SOP) and Work Practice (WP)management
- Curriculum definition and team training program
- Oversees relevance and timeliness on GMP-records in the quality management system, especially Corrective Action Preventive Action (CAPA), Deviation, Change Control (CC) management.
- Represents the purchasing and planning activities during site audits
Experience and Skills Required
- 10+ years’ experience in manufacturing logistics / supply chain
- 5+ years of leadership experience,
- University degree in Engineering / Supply Chain or MBA
- Experience in a GMP environment, understanding of GMP and FDA/EMA/Swissmedic regulatory requirements, capability to work with short deadlines
- Understanding of solid oral dosage forms manufacturing and packaging processes,
- Natural leader, at ease to take autonomously important decisions under pressure and to drive successful execution,
- Excellent change management and organizational skills,
- Strong analytical, problem solving, influential and deductive skills,
- Excellent IT proficiency: MS Office, Excel, ERP for manufacturing, procurement and planning,
- Strong verbal and written communication skills,
- Fluent in French and English
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 die Ressourcen bieten, ihre Ziele sowohl bei der Arbeit als auch in ihrem Privatleben zu verfolgen.
