Join Orano USA, where we're powering the future with innovation collaboration, and purpose. The Intern – Radiopharmaceutical Manufacturing will participate in the establishment of ATLab Indianapolis as a new commercial-scale manufacturing facility for therapeutic radiopharmaceuticals. The facility will be geared towards ramp up of activities to support Phase 3 clinical trials and commercial manufacturing. During Summer 2026, the facility will be concluding construction and qualification, so the Intern should focus efforts on: safety and occupational training, completing an assigned project, helping with basic tasks, growing in technical understanding, developing workplace skills, and building a professional network.

Key Responsibilities:

Safety and Compliance

• Read and follow all assigned relevant SOPs
• Safety: Reading/on-the-job training in radiation safety, hazardous materials, occupational safety.
• Assist with submissions and compliance for RAM license and environmental compliance.

Production, QC, Shipping

• Observe/assist with qualification of spaces: IQ/OQ/PQ of cleanrooms and aseptic spaces
• Assist with qualification (IQ/OQ/PQ) of new equipment and instrumentation.
• Observe and understand function of all instrumentation; chemistry behind production of Pb-212 and radiolabeled final drug product; science behind all QC methods.
• Assist with implementation of new software: inventory management, chemical inventory, eBR, LIMS, dose ordering, shipping software, etc.
• Consumable supplies: assist with inventory management, including planning, purchasing, inspecting, and accepting incoming supplies.
• Assist with design and implementation of shipping equipment and procedures.

Quality Assurance

• Embody and promote a culture of quality and continuous improvement.
• Adhere to all applicable procedures, cGMP, company policies, and any other quality or regulatory requirements.
• Learn about and gain comfort with cGMP and QMS.
• Assist with preparing and reviewing documents: SOPs, vendor qualification forms, material acceptance forms, instrument qualification forms, etc. 

Project

• In consultation with the supervisor, the Intern is expected to identify and complete a project with reasonable scope during the period of the internship.

Travel

• Amount: 1-3 optional travel opportunities
• The intern may receive other tasks and responsibilities as assigned.

Qualifications:

• Currently enrolled in a bachelor's program in pharmaceutical science, Pharm.D., Chemistry, Engineering, or a related field.
• GPA of 3.0 or higher
• Full-time student, completed 2+ semesters
• Strong attention to detail and interest in environmental compliance and safety.
• Good communication and organizational skills.
• Ability to work independently and as part of a team.
• Proficiency with Microsoft Office applications (Word, Excel, Outlook).

Why Join Orano?

At Orano, you’ll be more than “just an intern.” You’ll be part of a mission-driven team shaping the future of sustainable energy while gaining real-world HR experience. You’ll have the opportunity to innovate, contribute, and grow—personally and professionally—in an environment that values your voice.