Jobs at Bristol Myers Squibb

Leads cyber resiliency for a pharmaceutical manufacturing site, protecting IT, OT, automation, MES, and laboratory systems. Develops cyber risk strategies, recovery objectives, incident response processes, disaster recovery testing, ransomware exercises, and regulatory readiness. Partners with engineering, automation, quality, EHS, vendors, and cybersecurity teams to secure ICS environments and maintain GxP-compliant controls. Delivers awareness training and reports resiliency risks, KPIs, and recovery capabilities to site and enterprise leadership.

Leads the Quality Control Microbiology department supporting CAR T-cell therapy manufacturing. Oversees stability, raw material, in-process, final product, environmental monitoring, method validation, investigations, metrics, and data analysis. Manages personnel, training, scheduling, performance, development, budgets, and headcount. Ensures compliance with cGMP and global regulations, represents the department during inspections, supports laboratory design and lean initiatives, and provides on-call support for testing issues.

Leads cross-functional planning and execution for clinical-stage drug development programs. Builds integrated plans, manages timelines, resources, risks, dependencies, and regulatory milestones. Challenges assumptions, develops mitigation strategies, facilitates team meetings, aligns stakeholders, and escalates issues. Improves project management practices and applies AI to enhance execution and decision-making. Requires biotech or pharmaceutical experience and expertise advancing candidates through regulatory submissions.

Manage regulatory submission operations and PDF publishing to deliver high-quality, compliant eCTD submissions. Format and generate submission-ready PDFs, perform technical QC, track deliverables and timelines, coordinate vendors and cross-functional teams, support Veeva Vault RIM and reference management, and maintain regulatory submission standards and SOPs.

Ten-week paid finance internship supporting operating budgets, R&D portfolio allocations, financial forecasting, operating performance analysis, internal audit risk assessments, controls, and capital expenditure returns. Interns receive mentorship, professional development, and networking opportunities, with potential consideration for a full-time MBA Finance Associates Program role after graduation.

Field-based clinical expert who educates hematology and oncology healthcare professionals on BMS medicines, supports patient management and CAR T infusion sites, delivers approved clinical programs, develops HCP relationships, monitors account activity, and contributes to commercial planning. Requires frequent territory travel, clinical expertise in hematology/oncology and cell therapy, active nursing licensure, and OCN certification.

Provides scientific and technical expertise for commercial and late-stage drug product and packaging processes. Supports investigations, root cause analysis, validation studies, technology transfers, lifecycle improvements, GMP documentation, CMC submissions, and defined technical workstreams. The role contributes to standards, control strategies, continuous improvement, and reliable compliant product supply while collaborating across sites and functions.

Design, build, enhance, and support enterprise Identity Governance solutions using SailPoint IdentityIQ. Responsibilities include application onboarding, connector and rule development, workflows, access certification campaigns, entitlement management, provisioning, platform troubleshooting, upgrades, compliance controls, and stakeholder collaboration. The role also evaluates AI-driven governance, access recommendations, risk scoring, anomaly detection, and analytics to modernize identity governance.

Leads global congress strategy and execution for the Neuroscience therapy area at Bristol Myers Squibb. Oversees congress planning, budgets, vendors, sponsorships, stakeholder alignment, compliance, innovation, and post-congress closeout. Manages a high-performing team and collaborates across Medical, Commercial, and global partners to deliver consistent congress experiences. Requires extensive pharmaceutical industry and congress operations experience, strategic leadership, financial management, cross-functional collaboration, and approximately 15–20% travel.

Provides on-site, shift-based quality assurance oversight for manufacturing, QC laboratory, warehouse, and packout operations. Reviews records, assesses discrepancies, approves deviations, performs verification, supports inspections, and ensures compliance with cGMP, approved procedures, aseptic techniques, and quality systems. The role also identifies operational issues, supports remediation, authors documents, assists with maintenance oversight, and helps integrate new team members.

Owns delivery and operationalization of pharmaceutical commercial data products. Translates roadmaps into backlogs and releases, coordinates technical and business stakeholders, supports data governance, modeling, catalog management, quality controls, documentation, and adoption. The role also monitors operational KPIs, manages data issues, supports vendors and SLAs, and contributes to budget and tooling decisions across commercial data domains such as Sales, Marketing, Market Access, Medical, Payer 360, and Customer 360.

Lead site master production scheduling and order release for cell therapy manufacturing; manage capacity planning (RCCP), scenario modeling, KPI/reporting, stakeholder coordination, continuous improvement, and on-call support to ensure patient material availability end-to-end.

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.

Lead the design and implementation of Generative AI applications and collaborate with teams to deliver AI solutions while ensuring security, performance, and scalability of cloud applications.

Senior Utilities Electrical Engineer responsible for supporting operation, reliability and maintenance strategy of site utility and electrical distribution systems in a regulated biopharmaceutical facility. Duties include technical troubleshooting, developing PMs and reliability metrics, vendor engagement and SLAs, performance monitoring, training operations, commissioning, and supporting shutdowns while ensuring safety, quality and regulatory compliance.

Owns and optimizes CyberArk privileged access infrastructure, SaaS operations, integrations, migrations, secrets management, and BeyondTrust endpoint privilege controls. The role develops automation, manages upgrades and policy models, troubleshoots complex issues, supports audits, approves privileged access decisions, and mentors engineers. It requires strong CyberArk engineering experience, SaaS migration expertise, scripting, API integration, and security operations knowledge.

Performs SOX testing of financial, operational, and compliance controls; evaluates control design and operating effectiveness; documents testing evidence and results; reports testing status to leadership; identifies risks, control deficiencies, and process improvements; and supports internal control enhancements and contingency planning while collaborating with cross-functional Finance teams.

The Senior Analyst in Trial Analytics focuses on trial-level analytics, data modeling, and forecasting to enhance clinical trial efficiency and support drug development. Responsibilities include managing analytics workstreams, collaborating across teams, and contributing insights for trial planning.

Owns the vision, roadmap, backlog, and ongoing development of BMS’s workforce planning product using Workday Adaptive Planning and Workday HCM. Builds and maintains integrations, models, security configurations, reports, and dashboards. Partners with People Organization, Finance, and technical teams to mature workforce planning toward scenario modeling, organizational design, and skills-based forecasting. Leads governance, testing, deployment, stakeholder enablement, platform innovation, and data quality improvements.

Lead day-to-day media operations for HCP and DTC campaigns: manage media taxonomy and governance, oversee tracking/pixel implementations, ensure data/reporting integrity (APIs, loopback files, channel-level data), enforce channel standards, coordinate agency integrations, maintain compliance with Privacy/Medical/Legal, manage SharePoint and access, and serve as operational project manager for major media initiatives.