Project Manager, Project Management

Bristol Myers Squibb - Indianapolis, IN

Hybrid - Indianapolis, IN

Chemical Manufacturing

About the position

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.

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.

Requirements

• 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.

Nice-to-haves

• 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.