Senior Specialist, Manufacturing Scheduling

At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. In this position the Sr Specialist, Manufacturing Scheduling will manage within a short and mid-term scope the logistical activity for the manufacturing sites he/she is responsible for. This mission will be led in close collaboration with the internal stakeholders. The Sr Specialist, Manufacturing Scheduling can act as a back-up of his/her peer. SKILLS/KNOWLEDGE REQUIRED Bachelor’s degree in Business or in Supply Chain with at least 3 years of experience in Supply chain (production or supply planning) Prior experience within an international industrial environment, with a preference for pharmaceutics or biotechnologies Strong levels of resilience, able to work under pressure in autonomy, drive for result and quality oriented, pro-active personality with an eye for anticipation and strive for continuous improvement Independent self-starter, able to work autonomously Quick process understanding, insight and visualizing, strong analytical and problem-solving skills Prior experience with LEAN management is an asset • Excellent IT proficiency: MS Office, Excel, ERP, Oracle experience is an asset Fluency both in French and English mandatory DUTIES AND RESPONSIBILITIES Translate Supply plans into detailed scheduled plan on a daily basis within the frozen period Manage the detail scheduling for assigned work-centers and follow-up on executions including non-routine requests Prepare and lead the weekly scheduling meeting Follow up the daily operations with all stakeholders (QA, QC, Validation, Production, Warehouse, Supply Chain, etc.). Track Work Orders from their creations to their releases Manage priorities based on business requirements and constraints with stakeholders Define and guarantee the execution of the mid-term plans including availability of materials and Master data set-ups Coordinate with stakeholders the stability plan execution Coordinate with stakeholders, not limited to, all variations and support the transition to success Act as key point of contact to coordinate make to order (MTO) repacking activity Manage the reprocess activity with stakeholders if required • Accountable for KPIs (On Time in Full (OTIF), Schedule Adherence, Right First Time (RFT), etc.) Challenge status quo. Actively participate in continuous improvement activities with other Departments Accountable for all assigned change control tasks and implementation due dates Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Bristol Myers Squibb 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.