Bristol Myers Squibb logo
Bristol Myers Squibb · Life sciences

Senior Manager, Program Management

Bristol Myers Squibb Indianapolis, IN Posted Oct 29, 2026
Location
Indianapolis, IN
Workplace
On-site / per employer
Posted
Oct 29, 2026

About this role

Life at BMS

At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly-owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer.

Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. From day one, expect to make an immediate impact—on our science, on our teams, and most importantly, on patients. Learn more about RayzeBio: https://careers.bms.com/rayzebio/

Essential duties and responsibilities include the following. Other duties may be assigned.

Structure and Governance

  • ✓Establish the program management structure, processes, systems, and tools for the site.
  • ✓Define and implement governance, including steering committees, stage gates, and change

control.

  • ✓Partner with the SLT to define site KPIs, and present program status and KPIs to the VP and GM,

the SLT, and key stakeholders.

  • ✓Establish sustained communication and alignment with the RayzeBio Global Project

Management organization and other functional PMOs, ensuring consistent information flow and

timely escalation to the proper leaders.

Planning and Oversight

  • ✓Partner with functions to develop and maintain project plans and schedules with clear timelines

and priorities, and define and manage the critical path across all key activities and projects.

  • ✓Monitor progress at an executive level across site expansion (new suites and technology

installations), continuous improvement, and compliance activities, to ensure the site can

support all planned clinical programs and their commercialization.

  • ✓Oversee multiple concurrent projects, making sound prioritization recommendations when

timelines compete.

  • ✓Maintain visibility of facilities expansion, regulatory submission, new product introduction (NPI),

BMS Internaland product transfer timelines across internal teams and external partners, as applicable.

  • ✓Standardize NPI timelines and milestones across process development, supply chain,

engineering, quality, regulatory, and production.

Risk Management and Collaboration

  • ✓Foster communication and collaboration among Manufacturing, Quality, Regulatory,

Engineering, Supply Chain, Process Development, and Finance.

  • ✓Maintain risk registers, escalate risks early, and track mitigation and contingency actions to

closure.

  • ✓Monitor manufacturing and release-related issues and escalate to the appropriate functions for

decisions.

  • ✓Coordinate technical, compliance, and business input to ensure programs are robust.

Data-Driven Insight

  • ✓Provide data-driven feedback to the Site LT on bottlenecks and opportunities, and collaborate

with the Site LT on action plans.

  • ✓Support scenario planning to optimize plant capacity for financial planning, demand changes, or

process upsets.

Budget and Financial Support

  • ✓Partner with site Finance and function owners to monitor project timelines, expenses, and

spend against plan.

  • ✓Support monthly actuals, the latest best estimate (LBE), upside and downside scenarios, and

long-range plan (LRP) schedules.

Applies AI to improve team execution and decision‑making

We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview

Indianapolis - RayzeBio - IN: $143,622 - $174,036

Originally posted by Bristol Myers Squibb. View original posting