Jobs at Bristol Myers Squibb

Oversee month-end, quarter-end, and year-end financial close processes across UK and Nordic markets. Manage internal, external, and tax audits; coordinate tax and transfer-pricing activities; support legal-entity budgeting and profitability adjustments; drive finance process improvements and ad hoc projects; collaborate with global finance teams; and maintain technical accounting expertise across US GAAP, local GAAP, and regulatory requirements.

Manufactures blood-derived cell therapy components in a cGMP cleanroom using cell culture, harvesting, and cryopreservation processes. Operates production equipment, performs aseptic connections and transfers, weighs materials, records batch data, and follows GMP, safety, and quality requirements. Supports deviation investigations, CAPA completion, inspection readiness, continuous improvement, and production logistics. Maintains training qualifications and may become a subject matter expert and trainer within manufacturing.

Develop and maintain AI, machine learning, statistical, and forecasting models for commercial demand planning. Analyze large datasets, monitor model performance, improve forecast accuracy, document workflows, and communicate insights to technical and business stakeholders. Collaborate with Finance, Commercial, Market Access, and Analytics teams to translate business needs into analytical solutions and support standardized forecasting tools and processes.

Perform routine aseptic cell therapy manufacturing operations for liso-cel CAR-T in a controlled cleanroom environment. Execute SOPs, batch records, electronic transactions, and GMP documentation; maintain environmental conditions; handle materials and equipment; follow safety and quality requirements; complete training; support process improvements; and author compliant manufacturing procedures. The role requires shift flexibility, gowning and PPE, handling human blood components in BSL-2/ML-1 conditions, and lifting or moving production materials.

Leads worldwide pricing analytics, budgeting, reporting, and market analysis across the pharmaceutical portfolio. Partners with global pricing, market access, finance, commercial, and regional stakeholders to support pricing strategy, launches, forecasting, governance, and portfolio decisions. Translates complex datasets into recommendations for senior leadership, develops dashboards and analytical capabilities, monitors market trends, and drives automation and continuous improvement across international markets.

Design and optimize bioconjugation strategies, linker chemistries, targeting ligands, and nanoparticle architectures for selective delivery systems. Characterize bioconjugates using analytical and purification workflows, evaluate how ligand presentation affects delivery performance, and collaborate with protein engineering, formulation, analytical, immunology, and pharmacology teams. Communicate scientific findings to leadership, influence program decisions, and mentor junior scientists in a multidisciplinary research environment.

Supports clinical development of oncology radiopharmaceuticals by contributing to trial design, protocol development, study execution, data review, regulatory submissions, and scientific reporting. Collaborates with Clinical Operations, Medical Writing, Data Management, investigators, and cross-functional teams. Helps organize data review meetings, prepare clinical documents, address study questions, and resolve moderately complex clinical trial issues. Requires up to 20% travel.

Leads BMS Mexico’s value, access, and pricing strategy for product launches and the marketed portfolio. Oversees HEOR studies, economic models, pricing proposals, reimbursement pathways, and submissions to Mexican health institutions. Manages a multidisciplinary team, develops launch access plans, anticipates regulatory and market risks, engages senior internal and external stakeholders, and ensures compliance with pharmaceutical regulations and company policies.

Supports CAR T production planning and scheduling by verifying inventory, maintaining material transaction records, preparing regulatory compliance reports, and coordinating supplier delivery schedules and forecasts. Tracks supplier performance, evaluates metrics, and helps implement corrective actions. Ensures material management activities comply with applicable laws, regulations, company policies, and traceability requirements.

Leads the Southeast region’s pharmaceutical sales organization, translating business and brand strategy into regional plans, goals, budgets, and execution priorities. Develops and manages District and Territory Business Managers, drives sales performance and productivity, builds relationships with healthcare stakeholders, allocates resources, manages change, and ensures compliance with company, industry, and regulatory standards. Oversees recruiting, talent development, accountability, and achievement of regional business results.

Executes integrated corporate affairs and communications programs for Switzerland and Austria, covering external and internal communications, media relations, corporate and brand reputation, disease awareness, employee engagement, digital content, patient advocacy, and stakeholder engagement. Develops messaging and narratives, manages agencies and budgets, supports issues and crisis communications, tracks KPIs, and collaborates with medical, commercial, regulatory, legal, market access, and global corporate affairs teams.

Leads corporate affairs and integrated communications strategy across Switzerland, Austria, Poland, Romania, Hungary, and the Czech Republic. Oversees external and internal communications, media relations, reputation and crisis management, scientific and brand communications, patient advocacy, policy communications, digital channels, and employee engagement. Provides strategic counsel to senior leaders, manages budgets and vendors, develops communications teams, and aligns country initiatives with regional and global priorities across pharmaceutical business functions.

Leads enterprise Management Review and Quality Council strategy, governance, meeting execution, action tracking, predictive quality analytics, risk mitigation, and process improvement. Partners across global Quality, Manufacturing, Regulatory, and Technical functions to identify emerging risks, improve KPIs, verify issue resolution, and develop data-driven tools. Supports executive and Board quality reporting, builds council leadership capabilities, benchmarks industry practices, and advances quality systems toward a proactive, predictive operating model.

Provide legal and compliance support for AI across its lifecycle: risk assessments, governance framework implementation, contract review, regulatory tracking, training, and audit readiness to enable responsible AI adoption in a regulated life sciences environment.

Lead the coordination and authoring of regulatory documents for submissions and approvals, ensuring integration of scientific and regulatory input from cross-functional teams.

Manages supply planning and execution for pharmaceutical products across internal and external manufacturing sites. Develops supply plans, maintains inventory and purchase orders, aligns demand with production, manages supply risks, and reports key performance metrics. Collaborates with global supply chain stakeholders, supports new product introductions and clinical supplies, maintains master data, and drives process improvement through digital planning tools, analytics, automation, and AI-enabled capabilities.

Performs pharmaceutical microbiological testing, including environmental monitoring, water sampling, bacterial endotoxin, total organic carbon, and conductivity analyses. Conducts aseptic laboratory work, investigates product and environmental excursions, maintains and calibrates laboratory equipment, documents results under GMP requirements, troubleshoots methods, supports inspections and method development, and trains other employees on laboratory procedures, safety, and compliance.

Lead direct tax for a portfolio of European markets, manage external advisers, prepare corporate tax returns and US GAAP tax provisions using TaxStream, advise finance stakeholders, support UK tax governance, monitor legislative change, and drive tax process standardisation and automation.

Lead operations for a GMP laboratory facility, coordinating analytical testing, stability teams, systems, equipment readiness, safety, training, continuous improvement, and regulatory inspection preparation. The role uses matrix leadership to align priorities, develop scientists, strengthen safety culture, and maintain an audit-ready, high-performing laboratory environment.

Manages supply chain operations between customers, intercompany and third-party sites, including order processing, invoicing, shipping documentation, logistics coordination, redeployments, data integrity, SAP transactions, and financial reporting. The role supports external manufacturing activities, resolves order and invoice discrepancies, coordinates product release requirements with Quality Control, and ensures compliance with distribution, regulatory, finance, EHS, and security procedures.