Intern – Radiopharmaceutical Manufacturing

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.

Our Full-Time Benefits

• Competitive compensation
• Health, Dental, and Vision insurance – with generous employer contributions
• 401(k) with employer matching and contribution amounts

• Life insurance and Short- and Long-Term Disability insurance provided by the company
• Generous Paid Time Off and holiday schedules
• Numerous Training and Development opportunities

• and more…

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.

Orano is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, citizenship, veteran status, marital status, sexual orientation, gender identity, genetic predisposition or carrier status or any other characteristic protected by law.