Jobs at Bristol Myers Squibb

As a Senior Manager at BMS, lead the deployment and management of analytics assets, collaborate with cross-functional teams, and implement CI/CD practices while ensuring robust data security and governance policies.

Lead the authoring of clinical and regulatory documents in Japan, managing timelines, compliance, and cross-divisional collaboration. Oversee the quality of deliverables and provide guidance to scientific writers.

The Sr. Director, HRBP leads strategic HR initiatives for the Neurology and Strategy & Innovation areas, driving talent management, workforce planning, and organizational design while collaborating with senior leaders and ensuring alignment with corporate HR strategies.

The Senior Manager, Government Affairs & External Liaison shapes BMS Korea's policy environment, develops engagement strategies, and builds stakeholder relationships to support business and patient access goals.

The OT Systems & Automation Engineer supports Process Automation systems governance and delivery solutions while ensuring compliance and operational efficiency. Responsibilities include collaborating on automation solutions, troubleshooting DeltaV systems, and providing support for digital plant systems.

Lead design, standardization, and optimization of global end-to-end payroll processes. Drive automation, ensure tax and regulatory compliance, embed controls, partner with stakeholders and vendors, deliver change management, KPIs and continuous improvement to enable touchless payroll and better employee experience.

Manufacture CAR-T cellular therapy products in a cGMP cleanroom following SOPs. Perform aseptic processing, cell culture maintenance and expansion, harvest, isolation, cryopreservation, tube welding, sampling, counts, and material transfers. Support batch records, deviations, CAPAs, quality investigations, inventory control, and on-time production on a shift schedule (onsite night shift).

Lead a team delivering HR workforce administration and data management across global shared services. Manage complex employee lifecycle events (LOA, time tracking, severance), maintain Workday data governance, perform audits and mass uploads, coach staff, drive root-cause analysis and process improvements, support organizational change projects, and ensure compliance with local regulations.

Provide regulatory advice and risk assessment for US commercial promotional materials and campaigns for assigned products. Ensure compliance with FDA, OPDP, PhRMA, and FTC guidance; lead Subpart E/2253 submissions and training; partner with Commercial, Medical, Legal, and Compliance; support labeling strategy; manage and develop team members and drive process improvements.

Design and deploy AI-powered, full-stack web applications and LLM-driven tools to streamline pharmacometric and clinical data workflows. Build interactive visualizations, automate data ingestion/cleaning/document handling, and support preparation of analysis-ready datasets and regulatory submission materials. Collaborate with cross-functional teams, evaluate emerging AI technologies, and ensure software quality, reproducibility, and scientific rigor.

Design, build, and maintain ETL and real-time data pipelines and data products (cloud-first). Ensure data quality, security, performance and scalability. Collaborate with architects, analysts, and data scientists, own end-to-end delivery, mentor teammates, and drive platform and product-based data engineering initiatives.

Lead design and execution of early-phase clinical pharmacology trials: draft protocols/ICFs, collaborate on CRFs and data review, author CSRs and regulatory submissions, develop site training and present at investigator meetings, monitor safety and clinical data trends, and partner with KOLs and cross-functional teams.

Lead U.S. and global lifecycle strategy and commercial execution for Reblozyl. Drive brand performance, cross-functional alignment, launch and indication planning, omnichannel customer engagement, and team development while partnering with Sales, Medical, Market Access, Analytics, and Finance to deliver business and patient outcomes.

Create and maintain finite schedules for CAR-T manufacturing operations, coordinate cross-functional partners to ensure on-time product fulfillment, perform ERP lot and batch record tasks, support system implementations and continuous improvement, and provide on-call support for emergent issues.

Perform set-up and operation of equipment to produce cell therapy blood components in a cGMP cleanroom. Conduct aseptic processing, weighing/measuring, data recording, deviation/CAPA support, and safety-compliant manufacturing tasks. Maintain training, become SME/trainer in assigned functions, and support continuous improvement and inspection readiness.

Design and synthesize novel small molecules for oncology targeting protein homeostasis and induced proximity. Apply advanced organic and medicinal chemistry methods, and integrate computational, machine learning, and automated/parallel synthesis approaches to drive compound discovery and optimization.

Lead site capital project processes for a new cell therapy facility, managing project selection, budgeting, cost control, execution, and compliance. Oversee capital and expense portfolios, ensure regulatory compliance with F&E SMEs, implement novel solutions, track KPIs, and staff project teams including contingent workforce and some direct senior project management.

Oversee technology strategy for molecular design and optimization, ensuring integration of AI/ML in R&D workflows. Lead cross-functional teams to enhance drug discovery processes.

Lead data engineering for clinical operations: design, build, and optimize Databricks-based cloud data platforms and ETL/ELT pipelines; enforce governance and lineage; develop semantic models and GenAI/LLM applications (RAG, embeddings) to accelerate trials; collaborate with clinical and BI teams and mentor engineers.

Design, develop, and deploy AI/Copilot solutions using various Microsoft and AWS technologies, integrating AI search capabilities and ensuring solutions meet security and compliance standards.