The Senior Director oversees the oncology small molecule portfolio, guiding the design and optimization of assays and leading a multidisciplinary team in drug discovery efforts.

The Bioprocess Associate will work on manufacturing assignments, adhere to Good Manufacturing Practices, monitor processes, and train in operating production equipment and automation systems.

The Upstream Senior Bioprocess Associate operates bioreactors and chromatography skids, adheres to GMP regulations, monitors processes, and collaborates with teams to maintain production standards.

The role provides programming leadership for clinical projects, develops and maintains statistical programs, prepares submissions, and manages a small team, ensuring process improvements and team development.

The Director, PV Global Process Lead, will oversee pharmacovigilance processes, drive strategies, and enhance cross-functional collaboration within Patient Safety.

The Senior Software Engineer will analyze data, develop AI models, build APIs, and collaborate with teams to integrate generative AI into products.

Assist in developing and implementing team initiatives in Corporate Affairs, focusing on engagement strategies and project management tasks.

The intern supports assay design, development, and validation while collaborating with scientists, performing laboratory experiments, and analyzing data for a potency functional characterization assay.

Lead Safety Quality Management activities at BMS, ensuring compliance with GVP/GPSP requirements, managing audits, fostering a culture of quality, and driving strategic initiatives.

As a Senior Manager, Platform Developer, you will lead a team in managing AWS infrastructure, optimizing cloud resources, and developing performant Python and ReactJS applications, ensuring compliance with security practices and collaborating across teams.

The Procurement Analyst will manage sourcing and contracting processes across Commercial categories, ensuring effective purchasing and compliance while collaborating with stakeholders and driving continuous improvements.

Develops and implements provincial policy and access plans for funding BMS products in Ontario, partnering with health-system stakeholders to enhance patient access and outcomes.

The Senior Director, Program Management is responsible for leading high-priority drug development projects, executing integrated development strategies, managing teams, and ensuring alignment across sub-teams and governance levels.

The Senior Director, Policy Research will lead policy initiatives, manage the research budget, oversee vendor relationships, and translate research findings into actionable insights within Bristol Myers Squibb's advocacy framework.

Lead a team overseeing public and private payer reimbursement while developing national policies and engaging in federal government affairs. Ensure timely access to innovative therapies and maintain funding of BMS products across Canada.

The IP Paralegal / Global Filing role involves managing patent prosecution processes, ensuring compliance with filing requirements, and supervising the filing of patent applications worldwide.

The HR Advisor serves as the primary contact for HR queries in the EMEA region, providing policy advice and support for HR processes to employees and managers, while working with AI tools and ensuring data accuracy in systems.

The Senior Manager will lead international market analytics operations, oversee team management, enhance collaboration, and drive innovation while engaging with senior stakeholders to align with business priorities.

The Hospital Delegate is responsible for promoting medication to healthcare professionals, ensuring safety data compliance, and developing sector action plans.

The role involves overseeing clinical trials, project management, vendor coordination, and ensuring quality deliverables within established timelines and budgets.