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Bristol Myers SquibbPosted 2 weeks ago

Senior Manager, OSD Master Data Management

On-siteBoudry, Neuchâtel, Switzerland

Full TimeSenior LevelEnterprise

Job Summary

Drive end-to-end accountability for OSD Manufacturing Master Data accuracy, GMP compliance, and continuous improvement across the Boudry site. Lead the multi-year master data roadmap aligned with Global Supply Chain and IT priorities, while managing complex site programs including SAP S/4HANA readiness, ERP modernization, and Bill of Materials rationalization. Serve as the primary interface for Global Supply, IT/Digital partners, and cross-functional teams to resolve ambiguous issues and define global standards. Act as the deputy for the Director of Site Supply Management, overseeing team performance, talent development, and operational risk mitigation. Ensure full compliance with GxP regulations and regulatory inspection readiness through rigorous quality system record maintenance. This role operates within a site-essential 100% onsite environment at Bristol Myers Squibb's Boudry facility, supporting the broader objective of transforming patients' lives through science.

Required Qualifications

  • 12+ years of progressive experience in master data management, ERP, or supply chain operations, with a significant portion in a GMP/pharmaceutical manufacturing environment
  • 5+ years of people management experience, including management of senior specialists
  • Demonstrated experience leading complex ERP-related master data activities (SAP S/4HANA or equivalent), including data migration, governance design, and cross-functional coordination
  • Strong expertise in master data domains relevant to pharmaceutical manufacturing: Bills of Materials, Recipes, Routings, Production Versions, Batch Classification, Material Master, Plant Maintenance data
  • Proven ability to operate autonomously and strategically in a complex, international, multi-site manufacturing organization, managing ambiguity and competing priorities
  • Strong knowledge of GxP, GMP regulatory environment, and data integrity requirements applicable to pharmaceutical manufacturing
  • Demonstrated ability to develop and execute improvement roadmaps, drive change management, and deliver measurable results in a cross-functional environment
  • Strong leadership, coaching, and organizational development skills; proven ability to build and sustain high-performing teams
  • Strong analytical and problem-solving capabilities; proficient in leveraging data and metrics to support organizational decision-making
  • Experience deploying data quality frameworks, process excellence methodologies (Lean, Six Sigma), and digital analytics tools (Power BI, SAP Analytics Cloud, or equivalent)
  • Excellent interpersonal, communication, and influencing skills across organizational levels and cultural contexts
  • GxP mindset and quality culture deeply embedded in professional practice
  • Fluency in both French and English (written and spoken) is required
  • Advanced MS Office, Excel, SAP ERP/S4HANA, Oracle or equivalent ERP platforms; data analytics tools
  • 100% of shifts onsite at your assigned facility

Desired Qualifications

  • Project management experience (PMP, Prince2, or equivalent) and/or product lifecycle management expertise are an asset
  • Advanced data analytics tools are a strong asset

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