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Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

RayzeBio, a Bristol Myers Squibb company, is a dynamic biotechnology company headquartered in San Diego, CA. The company is focused on improving survival of people with cancer by harnessing the power of targeted radioisotopes. RayzeBio is developing innovative drugs against targets of solid tumors. Led by a successful and experienced entrepreneurial team, RayzeBio aims to be the global leader in radiopharmaceuticals.

RayzeBio is looking for a motivated and experienced Project Manager to oversee multiple projects at their Indianapolis manufacturing site. The role involves ensuring the completion of project timelines and key deliverables, particularly in the context of clinical programs. This position will require a blend of technical knowledge in logistical process planning, production efficiency, project coordination, and the ability to effectively communicate plans to ensure successful execution. The Project Manager will manage internal stakeholders to ensure production schedules meet customer demand. The Project Manager will report directly to the Sr. Manager of Program Management.

Key Responsibilities:

• Manage day-to-day project activities and escalate issues across multiple departments.

• Communicate project status effectively to senior management and stakeholders.

• Oversee logistics and planning to meet clinical and commercial production timelines.

• Serve as the primary contact for assigned programs, facilitating team discussions and decision-making.

• Manage multiple large projects with minimal supervision.

• Develop contingency and risk mitigation plans based on project requirements.

• Proficiency in project management tools and software applications (SmartSheet, Excel, ERP systems) for planning, analysis, and reporting.

• Effectively communicate and present project status to Sr. Manager of Program Management and key stakeholders.

Education & Experience:

• Bachelor’s degree with 3-5 years of experience in a relevant scientific field.
• Experience with Good Manufacturing Practices (GMP).
• Understanding of clinical trial design and FDA clinical trial processes.

Skills and Qualifications:

• Fluency in English.

• Proficient in MS Office Suite. Familiarity with ERP systems (e.g., SAP) is desirable.

• Understanding of radiopharmaceutical production processes is a plus.

• Strong long-term planning and cross-organizational management skills.

• Ability to protect and maintain confidential information.

• Excellent organizer, multi-tasker, and analytical person.

Physical Demands

While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision and distance vision.  Must be willing to wear personal protective equipment (PPE) for long periods.

This is a position that requires working in a laboratory environment, protective clothing, gloves, and safety glasses are required while working in a laboratory environment with radioactive materials.

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