Radiopharma Project Engineer – GMP & Automation

Bristol Myers Squibb; Indianapolis (IN); On-site; USD 82,000 - 100,000; Full time

Benefits offered by this job

Health Coverage

401(k) Plan

Paid Time Off

Job summary

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, is recruiting a Project Engineer for Indianapolis operations. You will oversee capital projects, upgrades, automation, and GMP system integration, coordinating cross-functional teams throughout project lifecycles.

The role requires a BS in Engineering and at least 3 years of engineering experience, with on-site work in a radiation-controlled environment. Travel up to 15% and strong documentation skills are expected.

Qualifications

• BS degree in Engineering required.
• Minimum 3 years of engineering experience, preferably in the pharmaceutical industry.
• Ability to work on-site in a radiation-controlled environment.

Responsibilities

• Coordinate and execute capital and facility expansion projects related to radiopharmaceutical manufacturing.
• Monitor project schedules and budgets, supporting timely completion of key tasks.
• Apply mechanical, electrical, and industrial engineering principles to assigned projects.
• Support design and implementation of commercial production lines and associated systems.
• Contribute to process automation projects to improve operational efficiency.
• Coordinate with vendors, partners, and service providers to meet project objectives.
• Promote compliance with EHS and Radiation Safety programs.

Skills

Project management

Cross-functional teamwork

Presentation skills

Time management

Drawing interpretation

Education

BS Engineering

Job description

RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, is recruiting a Project Engineer for Indianapolis operations. You will oversee capital projects, upgrades, automation, and GMP system integration, coordinating cross-functional teams throughout project lifecycles.

The role requires a BS in Engineering and at least 3 years of engineering experience, with on-site work in a radiation-controlled environment. Travel up to 15% and strong documentation skills are expected.