Jobs at Bristol Myers Squibb

Leads enterprise-wide aseptic process, sterility assurance, microbial risk, and contamination control strategies across pharmaceutical manufacturing sites. Governs media fills, smoke studies, sterilization, environmental monitoring, hygienic design, site assessments, quality decisions, CAPA, regulatory inspection support, and capital project oversight. Establishes standards for facilities, equipment, utilities, technology transfers, and sterile manufacturing while driving continuous improvement and innovation across global, matrixed teams.

Leads complex, cross-functional global supply chain transformation projects and programs. Responsibilities include portfolio planning, business cases, governance, risk mitigation, stakeholder communications, change management, digital technology evaluation, scenario analysis, budget and timeline management, and team leadership. The role supports strategic initiatives, drives operational excellence, and facilitates executive decision-making across global teams, with up to 20% travel for project-based workshops.

Support the design, development, testing, deployment, and operation of AI and generative AI solutions using AWS and enterprise platforms. Contribute to application integration, API development, data connectivity, DevOps, CI/CD, infrastructure automation, model monitoring, security, and compliance. Collaborate with cross-functional stakeholders, create technical documentation, support training and AI adoption, participate in agile delivery, and explore emerging technologies through innovation and proof-of-concept initiatives.

Leads regulatory intelligence, compliance assessments, governance standards, inspection readiness, and sterility assurance activities across BMS commercial manufacturing. The role interprets global regulations for aseptic processing, contamination control, and microbial quality; develops enterprise procedures and inspection materials; supports Health Authority engagements; oversees CMO/CDMO standards; and drives training, cross-site learning, and implementation of contamination control and sterility assurance frameworks.

Leads enterprise-wide aseptic processing, contamination control, sterility assurance, microbial quality, regulatory intelligence, inspection readiness, and compliance strategy across internal and external pharmaceutical manufacturing networks. Owns governance frameworks, regulatory alignment, CMO/CDMO oversight, training and qualification programs, risk methodologies, performance roadmaps, and industry engagement. Serves as a senior technical escalation point and represents the company with health authorities, industry bodies, and external partners.

Leads microbiological and sterility assurance investigations across internal manufacturing sites and external manufacturing partners. Provides expert impact assessments, reviews root cause analyses and CAPAs, supports contamination control strategies, aseptic process simulations, validation, inspections, and regulatory submissions. Develops oversight tools, mentors microbiology and quality teams, and drives global standards for aseptic processing, environmental monitoring, and contamination control. The role requires up to 25% travel.

Leads aseptic process and facility design, sterile manufacturing process development, scale-up, qualification, validation, media fill programs, contamination control, and lifecycle improvement. Provides enterprise APS and smoke study oversight, ensures cGMP and global regulatory compliance, supports inspections and submissions, and partners with Quality, Manufacturing, Engineering, MS&T, and Validation teams. Serves as a technical subject matter expert for troubleshooting, deviations, capital projects, technology transfers, and cross-site standardization.

Supports contamination event investigations, sterility assurance, microbiological impact assessments, deviation and CAPA documentation, and quality risk assessments across internal and external pharmaceutical manufacturing sites. Reviews environmental monitoring, sterility testing, aseptic processing, and contamination control data; contributes to regulatory inspection readiness, SOPs, change controls, and GMP improvements. Collaborates with microbiology, quality, manufacturing, validation, and external partners while supporting compliance with FDA, EU GMP, USP, and ICH requirements. Requires up to 25% travel.

Provides enterprise leadership for aseptic operations, sterility assurance, contamination control, environmental monitoring, and microbial risk management across global pharmaceutical manufacturing. Owns governance, standards, KPIs, cross-site harmonization, contamination investigations, CAPAs, regulatory inspection support, CMO oversight, and facility design guidance. Serves as the senior technical authority for sterile and non-sterile manufacturing practices and leads long-term capability and compliance strategies.

Provides senior-level oversight and execution of global clinical trial supply strategies for investigational products. Responsibilities include forecasting inventory, coordinating packaging and labeling, managing distribution strategies, supporting regulatory and inspection-readiness activities, collaborating with vendors and cross-functional teams, addressing risks and changes, and ensuring timely delivery of compliant clinical supplies.

Executes global clinical trial supply strategies for investigational products. Coordinates clinical supply planning, packaging and labeling, inventory forecasting, distribution, procurement, regulatory requirements, use-date extensions, IRT specifications, inspection readiness, and issue resolution across internal teams, vendors, and study stakeholders.

Leads BMS's global microbiology quality and sterility assurance function across pharmaceutical, biopharmaceutical, cell therapy, radiopharmaceutical, and external manufacturing sites. Owns the enterprise Contamination Control Strategy, microbiological controls, regulatory compliance, inspection readiness, remediation, KPI governance, CMO oversight, and technical standards. Builds a global center of excellence, develops talent, supports capital planning, engages health authorities and industry bodies, and drives contamination prevention and aseptic assurance across the organization.

Leads the global S&OP capability across people, process, technology, and data. Drives cross-functional alignment among commercial, finance, manufacturing, and supply chain teams; standardizes and transforms end-to-end planning processes; manages capability roadmaps, KPIs, governance, training, and change adoption. Oversees digital process redesign using advanced planning and analytics platforms, promotes AI and machine learning adoption, ensures regulatory compliance and data integrity, and leads complex transformation programs in a highly matrixed pharmaceutical supply chain.

Lead GxP inspection readiness and run the Third Party Risk Management program for Global Procurement. Enhance TPRM platform adoption, deliver monitoring and leadership reporting, support vendor due diligence and mitigation, design training and change management, and drive continuous improvement across global, cross-functional teams.

Manages supply plans for pharmaceutical materials across internal and external manufacturing sites. Coordinates demand and supply alignment, inventory, purchase orders, production schedules, and supply risk mitigation. Uses SAP, planning systems, Excel, BI platforms, and analytics tools to monitor KPIs, support root cause analysis, maintain master data, and improve planning workflows. Collaborates with global supply chain teams and stakeholders on product launches, clinical supplies, regulatory changes, and continuous improvement initiatives.

Lead global serialization data operations: manage data exceptions, regulatory reporting, and technical solutions across sites, CMOs, 3PLs and customers. Drive analysis, mitigation, change management, dashboards, CAPA assessments, and continuous improvement to ensure compliant, robust serialization data processes supporting product launches and business transactions.