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Orano Med is seeking a detail-oriented QC Analyst to join our Quality Control team. In this role, you will conduct cGMP testing of final products, in-process materials, raw materials, and stability samples. You will maintain laboratories, assist in writing and optimizing methods, perform method validation, and qualify lab equipment as needed. Responsibilities Perform comprehensive testing on final products, in-process materials, raw materials, and stability samples. Execute a variety of testing methods including chromatography, spectroscopy, wet chemistry, and radionuclide assays Complete and review test records with accuracy and attention to detail Report any quality anomalies according to established protocols Perform deviation and laboratory investigations as needed Draft data summaries including Certificates of Analysis (CofA) and stability summary tables Update methods, technical reports, and investigations documentation Prepare testing reagents and maintain laboratory supplies and chemicals Conduct environmental monitoring (EM) sampling, incubation, and testing Assist in validation and/or development of analytical methods and techniques Participate in the qualification of QC laboratory equipment Package and send samples to contract laboratories Additional responsibilities as assigned

Present in the United States for 60 years, Orano USA is a leading technology and services provider to the U.S. commercial and federal markets. Orano’s activities in the U.S. include developing a uranium enrichment facility in Oak Ridge, TN; packages and transportation of uranium & nuclear fuel assemblies; fabricating & installing used nuclear fuel dry storage canisters and casks, conducting pool-to-pad used nuclear fuel transfers; providing solutions to the National Labs and to the Dept of Energy; and supplying U.S. nuclear energy utilities with uranium, conversion, and enrichment services. In the nuclear medicine field, Orano Med is at the forefront of research in nuclear medicine and is developing a new generation of targeted therapies against cancer using the unique properties of lead-212. Part of Orano’s mission to address future global energy challenges is being successfully driven right here in the U.S. with Orano Enrichment USA (OEU).  The project to design, license, and build this facility is called Project IKE (the Project). Orano USA is seeking a highly qualified and experienced Chief Financial Officer (CFO) to join its executive team and to be based in Oak Ridge, Tennessee with regular business travel to Bethesda, Maryland, from 2026 to 2027. The CFO will: Lead & shape the financial management organization of Orano USA (OUS), OEU and Orano Federal Services (OFS); Propose & implement solutions for the financial structuring and financing of Project IKE; Monitor the financial performance of Project IKE; Lead the Finance Shared Service department in the United States, including the mentoring, supervision and development of its personnel. The CFO will have the following responsibilities for OUS and its U.S. affiliates: Oversees & manages all financial functions in the United States for OUS and its affiliates; support financial operations; Follows the multi-year financial trajectory of the U.S. region developed from the Orano group Strategic Action Plan; Coordinates and leads the budgetary process, including the quarterly updates, of Orano USA and its affiliates (OFS, OEU); Controls and provides guidance on the financial aspects of the requests for proposal and contracts with customers and suppliers; validates the accounting treatment of the contractual transactions; Analyses and controls financial results of the businesses; reviews and challenges economic performance of all operational entities; provides recommendations and alerts if needed to the financial departments of the concerned Business Units and the Orano group. Finally, the CFO will be also responsible for the following activities, under the supervision of the CFO of the Chemistry-Enrichment Business Unit, for Project IKE: In charge of the relations with financial and/or strategic partners involved in Project IKE; Proposes and implements financing solutions for the execution of the Project, including financial support from the Department of Energy.

Orano Med, a subsidiary of Orano USA, is at the forefront of research in nuclear medicine and is developing new therapies against cancer. Based on its unique expertise in the extraction and purification of lead-212 (Pb-212) and radiolabeling technologies, Orano Med is developing innovative Pb-212-based treatments which consist of selectively destroying cancer cells while limiting the impact on surrounding healthy cells. The top priority for the Senior Production Operator will be routine production. This position presents the opportunity to help establish a new facility that will meet high standards for quantity, speed, and reliability. A competitive candidate will be energetic and motivated. Key Responsibilities Work with Production Supervisor, Management and MS&T team to improve the process Collaborate with the shift supervisor to ensure the shift is running efficiently while leading by example Collaborate with the shift supervisor to train and mentor other members of the team Writing/Reviewing/Executing relevant SOPs, Qualifications, and internal studies Implement new equipment, materials, software, systems Environmental qualifications of new cleanrooms Complete: reading SOPs, gowning qualification, media fills, process training, bioburden runs, PV runs, tech transfer Top priority: Daily routine production  Follow EHS regulations/guidelines: NRC (ALARA), OSHA, EPA, chemical, waste disposal, state/local regulations, etc. Manufacturing activities following SOPs, using proper aseptic technique Setup production; line clearance; clean/VPHP Troubleshoot urgent problems Mentor and cross-train new employees Identify, document, communicate failures/near misses\ Quality/continuous improvement Adhere to SOPs, company policies, regulatory requirements, laws Work closely with QC/QA to deliver quality products Assist with deviations, OOT/OOS, CAPAs, change controls, audits, inspections Cleanrooms: cleaning, EM, restocking Packaging/labelling/driving/shipping of radioactive product Routine radiation surveys, wipe tests Maintain paper/electronic batch records, equipment logs, other records Equipment: maintain, qualify, calibrate, prepare, report problems, troubleshooting Maintain stock of materials/supplies; obtain documentation for raw material release

Orano Med, a subsidiary of Orano USA, is at the forefront of research in nuclear medicine and is developing new therapies against cancer. Based on its unique expertise in the extraction and purification of lead-212 (Pb-212) and radiolabeling technologies, Orano Med is developing innovative Pb-212-based treatments which consist of selectively destroying cancer cells while limiting the impact on surrounding healthy cells. The top priority for the Production Operator II will be routine production. This position presents the opportunity to help establish a new facility that will meet high standards for quantity, speed, and reliability. A competitive candidate will be energetic and motivated. Key Responsibilities Work with Production Supervisor and Management team to improve the process Collaborate with the shift supervisor to ensure the shift is running efficiently while leading by example Collaborate with the shift supervisor to train other members of the team Writing and reviewing relevant SOPs Help ensure the site is in an audit ready state Perform routine cleaning/disinfection of the cleanroom suites Complete: reading SOPs, gowning qualification, media fills, process training, bioburden runs, PV runs, tech transfer Top priority: Daily routine productionFollow EHS regulations/guidelines: NRC (ALARA), OSHA, EPA, chemical, waste disposal, state/local regulations, etc. Manufacturing activities following SOPs, using proper aseptic technique Setup production; line clearance; clean/VPHP Troubleshoot urgent problems Identify, document, communicate failures/near misses Quality/continuous improvementAdhere to SOPs, company policies, regulatory requirements, laws Work closely with QC/QA to deliver quality products Assist with deviations, OOT/OOS, CAPAs, change controls, audits, inspections Collaborate with MS&T and process engineers to identify process improvements and help execute development work needed to implement change Cross-train and performCleanrooms: cleaning, EM, restocking Routine radiation surveys, wipe tests OtherMaintain paper/electronic batch records, equipment logs, other records Equipment: maintain, qualify, calibrate, prepare, report problems, troubleshooting Maintain stock of materials/supplies; obtain documentation for raw material release

Orano Med, a subsidiary of Orano USA, is at the forefront of research in nuclear medicine and is developing new therapies against cancer. Based on its unique expertise in the extraction and purification of lead-212 (Pb-212) and radiolabeling technologies, Orano Med is developing innovative Pb-212-based treatments which consist of selectively destroying cancer cells while limiting the impact on surrounding healthy cells. The top priority for the Senior Manager, Production is to provide strategic and operational leadership for all GMP radiopharmaceutical manufacturing activities at ATLab Indianapolis. This role is accountable for ensuring the reliable, compliant, and efficient execution of clinical and commercial production, while developing the long-term capabilities, systems, and culture needed to support site growth. Key Responsibilities Leadership & Oversight Provide strategic direction, coaching, and performance management for Supervisors, Operators, and technical production staff. Drive operational excellence and accountability by setting clear departmental strategies, goals, and KPIs aligned with site and corporate objectives. Build and develop organizational capability through succession planning, training programs, and leadership development. Serve as a key member of the Site Leadership Team, providing input into site-wide strategy, planning, and resourcing decisions. Production Operations Oversee end-to-end production operations to ensure reliable supply to clinical and commercial customers. Direct planning, scheduling, and resource allocation to meet short- and long-term production needs. Ensure production readiness, including equipment qualification, material availability, facility readiness, and operator certification. Provide oversight and technical leadership during complex operations, atypical events, and high-risk activities. Quality, Compliance & Safety Ensure all operations adhere to cGMP, NRC, ALARA, OSHA, EPA, and state regulations. Elevate quality culture by driving excellence in documentation, investigations, change management, and audit readiness. Serve as a senior point of escalation for deviations, CAPAs, and risk assessments; ensure timely and effective closure. Partner with QA, QC, EHS/ RSO, and Regulatory Affairs to support inspections, license management, and site certifications. Continuous Improvement Lead cross-functional initiatives to improve yield, reduce cycle time, strengthen process capability, and optimize resource utilization. Apply Lean, Six Sigma, and Operational Excellence methodologies to eliminate waste and reduce variability. Drive introduction and governance of new technologies, systems, and digital tools to enhance operational efficiency. Other Responsibilities Provide leadership and input into site-level strategy, expansion projects, and long-range planning Oversee departmental budget planning and financial stewardship. Support hiring, onboarding, and organizational plan

Orano Med is seeking a detail-oriented EHS Specialist for radiopharmaceutical manufacturing at ATLab Indianapolis (“ATLab IND”), a new facility for commercial-scale manufacturing of sterile therapeutic radiopharmaceuticals. The EHS Specialist will be responsible for supporting safe, compliant, and efficient radiopharmaceutical manufacturing operations by implementing, monitoring, and improving Environmental Health & Safety programs. This role ensures compliance with NRC, FDA, DOT, OSHA, EPA, and state regulations, while fostering a strong safety culture in a highly regulated GMP environment. Key Responsibilities Develop, implement, and maintain EHS policies, procedures, and training tailored to radiopharmaceutical production. Monitor radiation safety programs, including dosimetry, contamination surveys, exposure tracking, and waste management. Support Radiation Safety Officer (RSO) activities and assist with maintaining compliance with RAM license conditions. Conduct safety inspections, risk assessments, and job hazard analyses; recommend corrective and preventive actions. Oversee proper handling, storage, transport, and disposal of radioactive and hazardous materials in accordance with NRC, DOT, and EPA requirements. Investigate EHS incidents, near misses, and deviations, document findings and lead root cause analysis. Partner with Quality, Operations, and Engineering to ensure compliance with FDA cGMP and ALARA principles. Maintain records and prepare reports for regulatory agencies (NRC, OSHA, EPA, state regulators). Provide EHS training and mentorship to manufacturing staff to promote a culture of continuous safety improvement. Schedule Monday through Thursday: 10:00AM-8:30PM

Join Orano’s IKE Project in Oak Ridge, Tennessee, a major investment strengthening the U.S. nuclear fuel supply chain through development of a state‑of‑the‑art enrichment facility delivering LEU to U.S. reactors. As EPC Project Manager, you will support the project through detailed design, procurement, construction, and commissioning, providing leadership to coordinate disciplines, vendors, and contractors while ensuring alignment with technical, financial, and regulatory requirements. This role ensures structured governance, communication, and proactive risk management to meet Orano’s standards for safety, quality, schedule, and performance.   The EPC Project Manager will be based in Lenexa, KS and Oak Ridge, TN, with regular travel required between the two locations.  What You'll Be Doing:  Lead the Orano EPC Project Management team overseeing Major Contractors through Engineering, Procurement, Construction, and Commissioning.  Apply Orano Project and Contract Management principles to ensure safe, on‑schedule, on‑budget execution aligned with licensing, permitting, and quality obligations.   Coordinate Procurement Requisitions, Change Orders, Engineering Change Requests, claims, and invoice approvals with the Project Management Organization and Supply Chain.   Work closely with Orano senior management, IKE project staff, regulators, and Major Contractors to maintain alignment across all project phases.   Support development and consistent application of Design and Construction Management processes across multiple geographically dispersed sites.   Develop and implement solutions to technical and contractual challenges to maintain design and construction progress.   Escalate issues and recommend solutions to the Project Director and senior management.  Manage and track safety, quality, schedule, scope, cost, and risk KPIs and provide clear, accurate upward reporting.   Interface with internal divisions and assist HR/Talent Acquisition with recruiting and onboarding project personnel.   Manage assigned projects to budget and lead Integrated Risk Analysis with Major Contractors, developing mitigation strategies and maintaining the project risk profile.   Assess project needs, resources, and challenges; address potential cost overruns, delays, or scope changes.   Monitor progress, milestones, and conditions affecting project cost or schedule and provide oversight to ensure Major Contractors meet financial, schedule, deliverable, and safety targets.    Key Relationships  Supervision Received – Project Director  Supervision Given – Project Managers  

The Associate Director, Quality will be responsible for driving technical excellence and regulatory compliance at ATLab Indianapolis, a next-generation commercial-scale facility for sterile radiopharmaceutical manufacturing. This position plays a critical cross-functional role in ensuring the facility operates with maximum reliability, safety, and regulatory readiness, contributing directly to the timely and compliant delivery of life-saving therapies. The Associate Director, Quality supports the company’s short- and long- term goals for maintaining Quality Systems and Compliance. This position provides direct oversight for the evaluation, implementation, execution and follow-up on quality systems in support of GMP compliance and release of finished product. This role oversees quality assurance of the manufacturing and packaging processes and procedures, the final review of investigations, and appropriate implementation of corrective actions to prevent recurrence. This role also provides input into the overall decision-making process pertaining to quality problems, internal and external, that can have far reaching results in terms of rejected batches, stock withdrawals, quarantined goods, revised production and marketing schedules and added manufacturing costs. Job Duties: Provides daily oversight of the QA teams responsible for supporting all production/processing areas. Develops and monitors appropriate KPI's for batch documentation review, Right First Time (RFT) and support of timely batch release. Responsible for department resource planning, talent development, and budget administration with regards to QA personnel. Directs investigations of product complaints and manufacturing discrepancies for manufactured products and ensures completion of appropriate documentation. Performs review of root-cause analysis and other problem-solving activities to identify effective corrective and preventative actions and appropriate effectiveness measures. Provides QA review and approval of Investigations, CAPAs, SOPs, Change Controls, and protocols/reports. Ensures completeness, accuracy and compliance of all documentation. Coordinates the preparation, review, and approval of the Annual Product Quality Reports and any established metrics / KPIs. Participates in Regulatory/FDA inspections and audits by providing information or expediting/obtaining information required by the inspectors/auditors. Schedules and conducts pre-inspection review of operations and follow-ups where corrective action is required.

Position Summary The Contract & Procurement Coordinator supports the Supply Chain Director and Work Package Managers in the administration, monitoring, and coordination of all procurement and contract-related activities associated with the EPC Contractor and project design development and work packages. This role ensures that contractual obligations, purchase orders, change events, and documentation flows are accurately tracked, controlled, and aligned with project milestones. Key Responsibilities 1. Contract Administration & Tracking (Primary Duty) Act as the supply chain liaison to EPC/Work Package Managers for all contract-related matters. Maintain the master contract register and track EPC contract commitments, deliverables, milestones, and changes. Monitor contract performance indicators (schedule adherence, deliverable receipt, commercial exposure, change trends). Prepare summary reports highlighting risks, required actions, and upcoming decision points. Support development of contract modifications, claims, amendments, and notices (NTPs, COs, NCR letters, clarifications, etc.) under direction of the Supply Chain Director. 2. Purchase Order (PO) Management Draft, issue, and update purchase orders in accordance with contract requirements and internal governance. Ensure PO amendments, change orders, and commercial adjustments are properly documented, approved, and logged. Coordinate with Finance and Accounting for invoice validation, accruals, and payment tracking. 3. Support to Work Package Managers Attend WP meetings as the Procurement/Contract representative. Track EPC vendor submittals, deliverable logs, and contractually required documents, ensuring timely receipt and compliance. Help manage the interface between technical work packages and commercial contract requirements. Maintain alignment between scope, schedule, and commercial commitments. 4. Documentation, Governance & Reporting Maintain organized and audit-ready contract files, correspondence, approvals, and purchase order records. Support the rollout of supply chain processes, templates, and standard operating procedures. Prepare weekly and monthly progress reports, KPIs, dashboards, and exception lists for leadership. Ensure compliance with internal procurement governance, delegation of authority, and contractual workflows. 5. RFP / Procurement Support (as needed) Assist with preparing RFIs, RFP packages, bid tabulations, and supplier communications. Help ensure alignment between EPC contract requirements and downstream procurement scopes. Track supplier pre-qualification and onboarding. 6. Cross-Functional Coordination Coordinate with Engineering, Project Controls, Finance, Legal, and Quality for contract deliverables, approvals, and risk items. Facilitate information flow between the EPC Contractor and internal stakeholders.

Orano, we’re not just powering the future—we’re engineering its foundation. As part of our groundbreaking uranium enrichment IKE Program, we’re redefining what sustainable nuclear fuel production looks like for the next generation. We’re seeking a Business Support Assistant:  Key Responsibilities Provide comprehensive administrative support to the management team Coordinate office logistics, including equipment management and workspace arrangements Serve as the primary point of contact for welcoming and onboarding new team members. Manage facility operations, including maintenance scheduling, vendor coordination, and workspace organization Maintain and update administrative systems and databases Arranges for entertainment of visitors and plan programs for executive meetings. Prepare correspondence, reports, and presentation materials using Microsoft Office suite  

Orano TN, a subsidiary of Orano USA, is a leader in the U.S. market for uranium transportation logistics and used nuclear fuel pool offload, dry fuel storage, and decommissioning waste transport. Along with offices in Columbia, Maryland, Orano TN has two manufacturing facilities in North Carolina for dry storage canisters and modules. Job Description: Orano TN is seeking a Plant Manager to manage operations in its nuclear fabrication group in Kernersville, NC. The Plant Manager will plan and direct plant policies, objectives, and initiatives, with profit and loss responsibility for the site; define and execute business plans; manage the operations to ensure production compliance, efficiency, quality, delivery, safety and cost-effective management of resources. Major Duties and Responsibilities: Leads the plant to achieve a safe, compliant, and productive operation that is rooted in the traits of healthy nuclear safety culture. Creates and implements staffing plans, promotes and mentors talents, and participates in internship program. Leads lean manufacturing initiatives and capital expenditure plan to improve productivity. Responsible for all production and facility-related expenses, and implements plan to control and reduce spending. Manages and evaluates the performance of management team members for compliance with established policies and objectives. Provides input for the strategic vision of the nuclear fabrication group, in particular staffing and investment plans to address new markets. Leads introduction of new products in the fabrication project management department and production line. Continuously assesses plant capacity and capability; plans, develops, and implements strategies for meeting production and financial goals. Develops and reviews operating dashboards, activity reports, and financial statements to determine progress and status in attaining objectives. Implements Orano group compliant policies, Orano TN policies, and required fabrication procedures; ensuring training is conducted for personnel.

Join Orano USA, where we’re powering the future with innovation, collaboration, and purpose. As a Human Resources Intern, you’ll gain hands-on experience in a dynamic corporate environment, working on meaningful projects that make a real impact. This is your opportunity to learn from seasoned professionals, sharpen your skills, and explore a career in HR. What You’ll Do Provide support for HR recruiting, including assisting with: Maintaining recruiting system records and candidate files Sourcing and outreach Scheduling interviews Reviewing and dispositioning applicants Initiating the onboarding process Provide support to employees by answering incoming questions on various HR –related topics. Support the One Orano initiative by developing innovative communications and activities to Bring awareness to highlighted celebrations. Work on special projects as directed Assisting with the review and update of internal job description Assisting with benchmarking roles for job posting and job offers Assist compensation team with project impacting all of US

Orano Med Theranostics Orano Med is seeking a detail-oriented GMP Manufacturing Technician We are seeking a highly motivated GMP Manufacturing Technician who will be responsible for non-clinical GMP manufacturing, maintaining the GMP suite and GMP equipment, as well as ensuring that all necessary documentation is maintained accurately in accordance with all applicable regulations. The GMP Manufacturing Technician assists with clinical material manufacturing as well as preparation for clinical product manufacturing. This position conducts routine maintenance of areas and equipment and maintains accurate records of operations within GMP suite. Key Responsibilities Follow written procedures for non-clinical manufacturing Complete batch records, forms, equipment logs, and other production records as directed per company procedures and GMP guidelines Work concurrently with Quality Assurance (QA) and Quality Control (QC) personnel to deliver a high-quality product Follow and adhere to production schedules and timelines Execute room and equipment preparation for manufacturing operations Perform room sanitization activities as needed to maintain controlled environment conditions Participate in isolator and room monitoring Participate in room and isolator preparation for manufacturing Stocking materials in the GMP labs Identify and communicate process and equipment failures during manufacturing to supervisor and equipment team Identify process errors and report to supervisor Participate in deviation investigations and follow management guidance for corrective and preventive actions Clean, sanitize and sterilize equipment and components to support production operations Initiate cleaning procedures for the labs, perform routine maintenance on equipment, restock labs. Demonstrate ability to perform tasks with minimal guidance once trained Complete training on Master Batch Records, Formulation Records, and Protocols related to non-clinical manufacturing Complete on the job training for cleaning, gowning, GMP suite access, and equipment Orano strives to provide a total compensation package that brings value to our employees. We also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off.

At Orano USA we are looking for a Security Program Manager that is responsible for developing, implementing, and overseeing the site’s physical protection, cyber security, and safeguards programs to ensure compliance with NRC regulations and to protect special nuclear material against theft, sabotage, or diversion. Core Responsibilities: Program Development & Oversight Establish and maintain the facility’s Physical Protection Plan in compliance with NRC regulations (10 CFR Part 73). Develop site-specific security procedures, training programs, and contingency plans. Ensure integration of physical, cyber, and personnel security measures. Regulatory Compliance Maintain compliance with NRC requirements for fuel cycle facilities, including safeguards and material control provisions. Prepare for and support NRC inspections and audits under the Fuel Cycle Facility Oversight Program. Implement corrective actions for any identified deficiencies. Security Operations Direct daily security operations, including access control, intrusion detection, and response force coordination. Oversee contractor security personnel and ensure they meet training and qualification standards. Coordinate with local law enforcement and federal agencies for incident response. Cybersecurity Implement NRC-mandated cybersecurity protections for digital assets at fuel cycle facilities. Monitor for vulnerabilities and ensure compliance with evolving NRC cyber rules. Safeguards & Incident Response Ensure protection of special nuclear material (SNM) against theft or diversion. Develop and test emergency preparedness and incident response plans. Act as the primary liaison with NRC’s Office of Nuclear Security and Incident Response (NSIR). Reporting & Documentation Maintain accurate records of security incidents, drills, and exercises. Submit required reports to NRC, DOE, and other agencies. Document compliance with NRC inspection manual requirements (IMC 2600).

Nuclear Facility Material Control and Accountability (MC&A) Specialist Responsible for ensuring that all nuclear materials are securely managed, accurately tracked, and fully compliant with national and international safeguards regulations. Core Responsibilities Inventory Management Develop and maintain systems to track all nuclear materials on-site.  Conduct regular inventories and reconcile discrepancies to ensure accurate records.  Regulatory Compliance Implement procedures in line with **10 CFR Part 74** (Material Control and Accounting of Special Nuclear Material).  Ensure compliance with NRC, DOE, and international safeguards requirements.  Data Analysis & Reporting Analyze material flow and measurement data to detect potential losses or anomalies.  Prepare mandatory reports on nuclear material status and submit them to regulatory bodies.  Security & Safeguards Prevent unauthorized access, diversion, or misuse of nuclear materials.  Support inspections and audits by NRC, DOE, or the International Atomic Energy Agency (IAEA).  Program Development Assist in the design and implementation of the facility’s MC&A program.  Establish protocols for measurement, control, and detection of special nuclear material.  Operational Support Work closely with operations teams to ensure nuclear material handling aligns with safeguards.  Provide technical expertise during facility modifications or new processes involving nuclear material. 

Orano, we’re not just powering the future—we’re engineering its foundation. As part of our groundbreaking uranium enrichment IKE Program, we’re redefining what sustainable nuclear fuel production looks like for the next generation. We’re seeking a Lead Mechanical Engineer to drive complex facility and process system projects from concept to reality. You’ll lead the mechanical engineering scope on a major nuclear project, serving as both a technical expert and a team leader. From design to execution, your work will ensure that our mechanical systems are safe, efficient, and built to perform — while coordinating closely with a range of disciplines to deliver fully integrated solutions. You’ll work shoulder-to-shoulder with elite engineers and regulatory experts, moving fast, solving hard problems, and making decisions that have real-world consequences. If you're ready to lead at the edge of what's possible in nuclear technology, we want to talk. Key Responsibilities Lead design, analysis, and specification of mechanical systems including piping, large mechanical equipment, and process machinery. Serve as the authority on mechanical systems, mentoring junior engineers and reviewing deliverables. Oversee and coordinate the work of the Engineering, Procurement, and Construction (EPC) contractor, ensuring compliance with design intent, safety, schedule, and quality expectations. Ensure all work aligns with key industry codes and standards (ASME, ANSI). Collaborate with cross-functional teams — including civil, electrical, I&C, and process engineers — to deliver cohesive, high-performance designs. Review and approve detailed calculations, equipment specifications, construction drawings, and technical reports. Perform site visits, field assessments, and mechanical inspections throughout design and construction phases. Anticipate, assess, and resolve technical challenges in mechanical systems and equipment integration.

Join Orano USA, where we’re powering the future with innovation, collaboration, and purpose. As a Human Resources Intern, you’ll gain hands-on experience in a dynamic corporate environment, working on meaningful projects that make a real impact. This is your opportunity to learn from seasoned professionals, sharpen your skills, and explore a career in HR. What You’ll Do Provide support for HR recruiting and Compensation, including assisting with: Maintaining recruiting system records and candidate files Sourcing and outreach Scheduling interviews Reviewing and dispositioning applicants Initiating the onboarding process Provide support to employees by answering incoming questions on various HR –related topics. Support the One Orano initiative by developing innovative communications and activities to bring awareness to highlighted celebrations. Work on special projects as directed Assisting with the review and update of internal job descriptions Assisting with benchmarking roles for job posting and job offers Assist compensation team with project impacting all of US

Orano Med is seeking a detail-oriented Technology Transfer Lead for radiopharmaceutical manufacturing at ATLab Indianapolis (“ATLab IND”), a new facility for commercial-scale manufacturing of sterile therapeutic radiopharmaceuticals. The Technology Transfer Lead will define the strategy and implement the framework for technology transfers of radiopharmaceutical products developed within Orano Med. Lead technology transfer projects between Orano Med sites, overseeing activities for both sending and receiving sites, in collaboration with all involved departments (Chemistry, Manufacturing, and Controls, Quality, Regulatory, MS&T and Operations) including: Responsibilities Project scoping: formation of the project team, timeline definition, specific cost assessment, and establishment of prerequisites and deliverables. Drafting and approval of technology transfer protocols (including analytical method transfer) as well as defining the validation strategy for implementing new processes. Conducting risk analyses and developing mitigation strategies, including cleaning validation and cross-contamination risk management. Monitoring project timelines and deliverables, reviewing generated documentation to ensure completeness and compliance with project needs. Assessing facility readiness and operational preparedness. Providing technical support and troubleshooting during site transfers, including root cause analysis of process deviations or anomalies. Ensuring full documentation traceability and robustness to guarantee regulatory compliance and industrial reproducibility. Addressing radiological safety risks in coordination with local Health, Safety, and Environment representatives. Manage outsourcing projects to Contract Manufacturing Organization/Contract Development and Manufacturing Organization partners for Active Pharmaceutical Ingredient (peptide or other) manufacturing, defining, and overseeing Chemistry, Manufacturing, and Controls requirements with external suppliers or partners. Prepare for and support audits and inspections (including health authorities’ inspections) related to technology transfers. Implement and promote best practices in technology transfer, capturing, and sharing lessons learned across the organization.  

Orano USA is offering a unique internship opportunity to contribute to strategic analysis in support of evolving U.S. nuclear policy. The Department of Energy is expected to release a comprehensive back-end strategy, and this internship will position you at the forefront of evaluating the technical, regulatory, and economic pathways for implementing such a strategy. Key Responsibilities: Using public documents and Orano’s internal expertise, the intern will: Spent Fuel Recycling Strategy Assess availability and distribution of spent fuel resources in the U.S. Evaluate the technological readiness of domestic industry players Identify areas where licensing French technologies could support U.S. implementation Review applicable laws and regulations that may require modification Analyze market barriers to recycled fuel adoption and propose solutions Examine final waste management strategies for recycled fuel byproducts Plutonium Inventory Valuation Strategy Assess the scale and characteristics of excess plutonium inventory Identify legal and regulatory changes needed to enable reuse Explore potential materials and technologies for blending plutonium into usable fuel Evaluate readiness of existing and emerging reactor technologies for plutonium-based fuel Analyze market barriers and propose strategies to stimulate demand Review final waste strategies for used plutonium-based fuel

Position Overview We're seeking an organized and detail-oriented project management intern to support our project management team. This internship provides exposure to the full project lifecycle, from initiation through closeout, and offers opportunities to develop essential project management skills. Key Responsibilities Assist project managers in planning, executing, and monitoring projects Track project timelines, budgets, milestones, and deliverables Coordinate meetings, prepare agendas, and document action items Update project schedules and maintain project documentation Support risk identification and issue tracking processes Prepare status reports and presentations for stakeholders Facilitate communication between project team members Help manage project resources and vendor relationships Assist with project closeout activities and lessons learned sessions