Jobs at Bristol Myers Squibb

Serve as Scrum Master for a Cloud Engineering team within the AI Hub, driving Agile adoption, facilitating cross-functional delivery of cloud/AI initiatives, removing impediments, tracking Agile KPIs, onboarding teams/vendors, and training stakeholders on Agile, JIRA, and intelligent workflows while ensuring compliance with governance standards.

Manage QC sample lifecycle including receipt, labeling, tracking, shipment, and inventory. Perform sampling and visual inspection of incoming goods, GMP documentation review, data verification, and support CAPAs, deviations, and continuous improvement. Use electronic systems (CELabs, SAP, SmartQC, LIMS/ELN) to document activities, maintain safe organized lab practices, and train others on duties.

Lead design and hands-on delivery of cloud-native, AI-enabled platforms on AWS. Build reusable IaC, serverless, multi-account solutions; mentor Cloud/DevOps teams; implement CI/CD, observability, networking, security, and disaster recovery. Drive API, frontend (React/GraphQL), scripting, and genAI integration while ensuring scalable, testable, and user-friendly systems.

Administer and maintain the CMMS (inputting PMs, asset tagging, reporting), schedule and coordinate preventive/reactive maintenance, oversee contractors, ensure GMP/EHS/NRC compliance, maintain records and spare parts inventory, support equipment commissioning/validation, and contribute to SOPs, deviation investigations, and CAPA activities.

Lead identification, shaping, and incubation of innovative market access and pricing models (PBM disruption focus). Manage innovation pipeline, develop pilot-ready concepts, engage external partners, connect intelligence to innovation, enable governance, and collaborate across access, pricing, legal, digital, and leadership to drive scalable solutions.

Prepare, negotiate, and finalize site contracts and investigator budgets per SOPs and templates; maintain contract records in CLM/e-signature systems; collaborate with Legal, Finance, CROs and study teams; meet KPIs for cycle time, quality and data accuracy; escalate complex or out-of-threshold items; support process improvements.

Lead planning, execution, and closeout of Phase I-III clinical trials. Manage CROs and vendors, oversee timelines, enrollment, site performance, data quality, budgets, and risk mitigation. Drive site feasibility/activation and cross-functional study teams, escalate issues, and support operational strategy. Travel up to 20%.

Develop and execute market access strategies for Emisar, OptumRx, and UHC. Build executive-level relationships with PBMs, GPOs, and payers; lead contract negotiations; communicate clinical and economic value propositions; monitor market intelligence and contracted product performance; and collaborate cross-functionally on access and pull-through strategies. Frequent travel of up to 50–65% is required, along with incorporating AI into role activities.

Performs cryopreservation, storage, movement, inventory control, chain-of-custody tracking, and disposal of patient materials for CAR T manufacturing. Executes batch records and maintains compliant documentation under cGMP, GDP, SOPs, and work instructions. Supports liquid nitrogen storage operations, investigations, deviations, CAPA activities, reporting, personnel readiness, and process improvements. Requires on-site work, staggered overnight shifts, overtime as needed, and cross-functional collaboration.

Manage R&D asset program finance, including governance support, budgeting, forecasting, study costing, actuals reporting, variance analysis, and month- and quarter-end close activities. Use Anaplan to update forecasts, evaluate assumptions, analyze financial performance, support study valuations, and maintain effective financial controls. Partner with development teams, R&D Finance leadership, and global stakeholders to ensure accurate reporting and timely delivery of financial objectives.

Implements and administers manufacturing training programs for cell therapy operations. Conducts instructor-led and on-the-job training, evaluates operator competency, maintains training records, develops SOPs and course content, and ensures compliance with GMP and regulatory requirements. Supports onboarding, scheduling, supplies, laboratory maintenance, and equipment checks. As needed, performs aseptic processing and manufactures clinical-grade cellular therapy products in ISO 7 and ISO 8 cleanrooms while supporting quality investigations and process improvements.

Leads strategic procurement and category management for Clinical Development specialized services, including Regulatory and Patient Safety. Responsibilities include sourcing, supplier evaluation and negotiation, category strategy, supplier relationship and risk management, cost reduction, budget oversight, governance, compliance, reporting, digital procurement improvements, and stakeholder alignment across R&D, Finance, Legal, and Clinical Development.

Cryopreservation operations specialist responsible for processing, storing, transferring, tracking, and disposing of patient materials used in CAR T manufacturing. Maintains chain of custody, inventory records, batch documentation, and GMP/GDP compliance. Supports liquid nitrogen storage operations, investigations, deviations, CAPA activities, reporting, personnel readiness, and process improvements. The role requires onsite shift work, flexible scheduling, and effective collaboration across manufacturing functions.

Leads full-cycle talent acquisition for corporate functions, partnering with hiring managers and HR leaders to align recruiting with workforce plans. Builds talent pipelines, influences hiring decisions, develops competitive offers, and enhances employer branding. Uses AI tools, ATS data, Tableau, and predictive hiring technologies to improve workforce planning and hiring outcomes while delivering inclusive, high-touch candidate experiences. Provides agile recruiting support in a fast-paced, cross-functional environment.

Designs and executes cell and molecular biology experiments to support oncology discovery. Leads large-scale and single-cell CRISPR screens, optimizes NGS library workflows, performs cloning, cell engineering, lentiviral transduction, flow cytometry and downstream assays, analyzes data, presents results, and coordinates with cross-functional teams.

Lead development and execution of QA and User Acceptance Testing (UAT) for IRT systems supporting clinical trials. Create test strategies/plans, define acceptance criteria, manage test assets, review requirements, report quality metrics, mentor staff, coordinate vendors, ensure regulatory compliance (cGMP, 21 CFR Part 11, ICH E6 R2), and drive multiple validations to timely delivery.

Lead and grow the separations group within Analytical Method Sciences to deliver and sustain chromatographic and electrophoretic methods for commercial biologics testing. Provide technical and strategic oversight for method development, validation, transfer, lifecycle management, regulatory submissions, and cross-functional alignment while building talent, driving operational excellence, and ensuring compliance with quality and GMP requirements.

Lead end-to-end development and productionalization of AI capabilities for HCP engagement: build predictive/optimization models, oversee HCP 360 data foundation and feature engineering, establish MLOps/CI-CD and governance for responsible AI, partner with stakeholders for delivery, and coach engineering and data science teams for operational excellence.

Designs and develops enterprise Microsoft Power Platform solutions using Power Apps, Power Automate, Dataverse, Power BI, AI Builder, and Copilot. Responsibilities include data modeling, security, integrations with Azure, Fabric, and Databricks, ALM and CI/CD, governance, gateway management, stakeholder collaboration, training, documentation, and end-user support.

Provides strategic and technical leadership for commercial radiopharmaceutical manufacturing science and technology. Leads technology transfers, process characterization, scale-up, process validation across Stages 1–3, CPV, SUPAC, APQRs, deviations, CAPAs, CMC regulatory support, and inspection readiness. Manages CDMO relationships, radiopharmaceutical manufacturing requirements, and the Indianapolis MS&T team while driving process robustness, yield, safety, and lifecycle improvements.