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Join Orano’s IKE Project in Oak Ridge, Tennessee—one of the largest private investments in state history. This advanced uranium enrichment facility will strengthen the U.S. nuclear fuel supply chain by producing low enriched uranium (LEU) for domestic reactors. The project is creating hundreds of high‑quality jobs and positioning Oak Ridge as a center for nuclear innovation. Working on the IKE Project means contributing to a mission grounded in technical excellence, sustainability, and national impact. To support project execution, Orano is seeking multiple experienced Area Project Managers to work alongside the Engineering, Procurement, and Construction (EPC) Project Manager. As the project moves through detailed design, procurement, and construction, Area PMs will manage defined scopes of work within the EPC contract. Orano plans to hire at least two Area PMs initially, expanding to as many as five as the project progresses. Each Area Project Manager will oversee a specific scope—such as process systems or facility buildings—from detailed design through procurement and construction. Reporting to the EPC Project Manager, Area PMs will track physical progress, manage contractual obligations, and coordinate with a matrixed organization to deliver their scope safely, on schedule, and within budget. This role is essential to maintaining accountability and performance across diverse technical areas.   This position is based in Oak Ridge, TN, with regular travel to Lenexa, KS, and Bethesda, MD.   What You’ll Be Doing:  • Oversee a defined scope area within the EPC contract, coordinating with matrixed resources across engineering, procurement, construction, and commissioning. • Apply Orano project and contract management principles to meet scope goals on schedule, within budget, and in compliance with safety, licensing, permitting, and quality requirements. • Coordinate with key stakeholders including the EPC Project Manager, Orano leadership, IKE staff, regulators, and the EPC Contractor. • Support consistent design and construction management processes across multiple sites in a Progressive Design‑Build environment. • Develop solutions to technical and contractual challenges to maintain EPC progress. • Escalate issues and recommend solutions when impacts extend beyond assigned scope. • Track schedule, cost, scope, and performance metrics; monitor safety, quality, and risk indicators; and provide clear reporting. • Collaborate across internal divisions and provide leadership to maintain scope‑area budget performance. • Lead integrated risk analysis, develop mitigation strategies, and manage risks within Orano’s corporate framework. • Assess scope needs, identify required resources, and coordinate with resource managers to meet performance targets. Key Relationships Supervision Received – EPC Project Manager Supervision Given – None (Matrix Organization)

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.

Across the nuclear fuel cycle, Orano has extensive expertise in cutting-edge technologies, high value-added products and services, and a strong capacity for innovation. Join us in shaping the nuclear energy landscape of tomorrow. Your skills and passion can help drive the innovation needed for an abundantly powered future! Orano Enrichment USA is seeking a Communications Specialist I for our office in Oak Ridge, TN. The Communications Specialist will directly support Orano’s Project IKE development of a uranium enrichment facility in Oak Ridge and will also serve as the company’s community liaison. Responsibilities include supporting the development and implementation of communication strategies through writing, editing, community engagement, and media relations. Major Duties and Responsibilities Support Orano’s Project IKE development through communications and community engagement, in particular with local high schools, colleges, and universities and regional municipalities, Industrial Development Boards, and business organizations Attend public meetings relevant to Project IKE Write and edit external communication materials, including press releases, articles, social media posts, presentations, talking points, and website content Serve as a point of contact for community stakeholders Support and attend regional events involving Orano’s Project IKE or corporate teams Monitor and help manage the organization’s public image Assist with media relations, including outreach and responding to media inquiries Ensure adherence to Orano’s branding, messaging, image, and graphics requirements Create and update internal communications content Assess, compile and format actionable metrics Perform special projects as assigned

Welcome to Orano Group! Join our Orano TN team to help meet current and future challenges to build the clean energy world of tomorrow. By joining the Orano Group, you will be a part of a leading international player in the nuclear industry. Orano TN is seeking a Proposal Manager for the Columbia, MD, office to support the Nuclear Material Back End solutions business line but may from time-to-time support proposals for Transportation, Logistics, and Packages Product Line focusing on the Front-End of the fuel cycle. Major Duties & Responsibilities: Identify and qualify opportunities, including development of teaming and capture strategy Produce proposal outlines, schedules, compliance matrix, and instructions for creating a proposal that meets the customer requirements and Leads proposal efforts from strategy to pricing to contract closure. Provide leadership and instructions to relevant SMEs in support of proposal writing Solicit all necessary costing information from the necessary stakeholders involved – i.e., Project Management, 3rd party companies, Engineering, QA, Legal, Finance, and other Orano divisions Develop and grow client relationships Build strategic relationships with industry teaming partners Lead proposal strategy and win theme development in coordination with the VP of Sales and Product line managers objectives Assess competition and potential markets consistent with company growth strategy, including research and analysis of business opportunities Develops or assists in developing the business strategies to enhance relationships and sales revenue in line with the VP of Sales and Product line managers strategic objectives Develop formal presentations for senior management review and approval in proposal process Interface with subject matter experts in coordinating proposal documents Consolidate responses from multiple authors/reviewers and ensure proposal message is clear throughout Perform desktop publishing in MS Word, and other tools (e.g., Adobe Acrobat, MS PowerPoint) to ensure proposal documents are properly formatted, compliant with solicitation requirements, easy to read, and visually appealing. Orano strives to provide a total compensation package that brings value to our employees. While the pay range lists the base salary, we also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off.  Please Note: The provided salary information is a guideline. Your offered salary is based upon experience, qualifications, geographic location, as well as market and business considerations. Salary range annually: $145,000-$175,000

TN Americas, a subsidiary of Orano USA, is a leader of the American nuclear dry storage market. The company offers a complete line of products and related services to the transportation, storage, and engineering sectors operating in the fuel cycle materials market. TN Americas is seeking a Project Manager for our Columbia, MD, location with at least 10 years of experience in the nuclear industry to lead the planning, execution, and oversight of complex transportation projects involving nuclear materials, used nuclear fuel, and radioactive waste. Under broad supervision, this position is responsible for securing and managing transportation services utilizing our product line of packages, containers, casks, and equipment. This role requires a deep understanding of regulatory, logistical, supply chain, and technical considerations related to the safe and compliant transport of nuclear materials. The ideal candidate will be results-driven, customer-focused, and capable of managing cross-functional teams to deliver successful outcomes from proposal development through contract closeout. This role also requires a deep understanding of the planning and execution of technical Feasibility Studies and consultancy reports, Demonstrated experience in multimodal transportation within the Canada market a strong plus. Major Duties and Responsibilities Provides project leadership for major commercial design, fabrication of packages, licensing and transportation projects, plus on-site operations. Develops proposals in response to customer request and secure contract awards in alignment with company goals. Coordinates closely with engineering, licensing, and operations teams to ensure timely and compliant project execution. Prepares project plans/schedules/materials to achieve project quality, reliability, cost and timing objectives. Maintains a high level of customer satisfaction, addressing concerns proactively and building long-term relationships to drive customer engagement and business growth. Serves as the primary point of contact for customers, internal stakeholders, and third-party service providers throughout the duration of the project. Utilizes approved project management methods and processes to execute medium risk projects of existing technology and methods to meet client needs and expectations. Develops assignments, timetables and responsibilities for team members for the duration of the project. Coordinates multiple project activities including organizing and directing personnel, materials and equipment; utilizes team building skills to ensure satisfactory project performance. Defines and forecasts needed skills to meet project objectives. Performs lead sales duties to expand business portfolio with assigned customers

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

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. Orano USA is seeking a dynamic and skilled Senior Recruiter with exceptional sourcing capabilities to join our HR team in Oak Ridge, TN. The ideal candidate will be a talent acquisition professional with proven expertise in identifying, attracting, and recruiting top-tier talent. Key Responsibilities • Recruit across technicals, professional, and administrative staff positions. • Leverage advanced sourcing techniques, with particular emphasis on LinkedIn and other professional networking platforms. • Develop and maintain robust relationships with educational institutions, professional networks (career fairs, jobs fairs, community events) and recruitment firms. • Collaborate closely with hiring managers to define precise candidate requirements.  • Conduct in-depth interviews and candidate assessments to identify the most qualified talent. • Extend job offers and coordinate candidate onboarding and relocation processes. • Manage and optimize the company's personnel advertising and recruitment marketing efforts. • Stay current with employment laws, staffing trends, and recruitment best practices.

Orano Med Theranostics Orano Med is seeking a detail-oriented CMC Scientist We are seeking a highly motivated CMC Scientist with expertise in radiopharmaceutical development to join our CMC team. The successful candidate will design, execute, and analyze studies and create reports for R&D CMC to support the development of novel radiopharmaceutical compounds. This role offers an opportunity to contribute to groundbreaking therapies and collaborate with cross-functional teams to advance our pipeline toward clinical trials. Key Responsibilities Design, conduct and optimize R&D studies to characterize radiopharmaceutical compounds. Analyze, interpret and troubleshoot complex datasets. Prepare summary reports to support tech transfer and regulatory filings. Review and further develop & refine existing processes. Collaborate with cross-functional teams review protocols, batch records, formulation records, and other related documents. Maintain accurate records of experiments and ensure data integrity in accordance with company policies. Stay current with advancements in radiopharmaceutical science and contribute to the development of innovative research strategies. Other duties, as needed. 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.

Orano Med Theranostics:   Are you passionate about ensuring the highest standards in pharmaceutical manufacturing? Do you thrive in a fast-paced, detail-oriented environment where your work directly impacts clinical trial success? Join our Quality Assurance team as a QA Specialist and play a vital role in safeguarding the integrity of raw materials and sterile drug products. Whether you're beginning your QA journey or seeking your next challenge, this is your chance to grow within a dynamic, mission-driven organization that’s transforming oncology from the inside out. The Quality Assurance Specialist will be responsible for supporting GMP manufacturing of raw materials and sterile drugs for clinical trials. The individual in this role will review documentation related to raw materials, components, and completed batch records followed by giving a disposition of each. Assist with quality systems improvements. Key Responsibilities Inspect, review documentation, and release incoming raw materials and packaging components. Update Quality SOP’S and perform secondary review of documentation. Perform area release for manufacturing, as needed. Oversee sterile manufacturing process, provide sterile gowning and practice instruction. Review production batch records, logbooks, and associated documentation to assess completeness, accuracy, and compliance with SOPs. Review of equipment and instrumentation documentation in support of GMP manufacturing and testing operations. Scanning manufacturing documentation such as batch records, raw materials, audits, investigations, CAPA, and change control. Release/disposition GMP products for Macrocyclics and OM. Follow up on investigations, CAPAs and change controls for time completion. Review of documentation related to technology transfer from R&D for manufacturing activities. Perform Internal audits of GMP labs and other non-GMP processes as directed. Additional responsibilities as assigned Schedule Work hours vary, start times possible as early as 12AM.

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. Orano USA is seeking a highly qualified and experienced Chief Operating Officer (CPO) to join its executive team and to be based in Oak Ridge, Tennessee with regular business travel to Bethesda, Maryland. The CPO is responsible for leading the successful execution of the IKE enrichment Project in the US.  The primary goal is to ensure the enrichment facility is licensed, built, and commissioned in line with the approved schedule, budget, and applicable regulations. The CPO will have the following responsibilities: Oversees the IKE Project execution and all related projects (enrichment facility, support facilities such as: laboratory, waste treatment facility…) on the Oak Ridge site; Oversees the Program definition and leads the corresponding approval process with the BU Coordinates all contractors and EPCs involved in the Project; Ensures compliance with the Project approved budget, costs and planning; Oversees all phases from licensing and design to construction and commissioning activities, as well as activities required to ensure protection of the operating plant; Ensures the compliance with the Project basic data requirements and configuration management; Manages the processes implemented to obtain the regulatory authorizations required in order to implement the project; maintains compliance with regulatory requirements; Monitors the Project risk management plan and associated action plan; Establishes performance metrics and milestones for the execution of the Project; Represents the Project and the Program: - at the Business Unit level within the required governance meetings and Project Steering Committee; - at the Orano group level committees when required (e.g. Executive Committee and the Major Project Committee); Leads, mentors, and supervises OFS personnel involved in the Project and OEU staff, directors, and executives; Fosters a high performing culture and oversees recruitment, training, and retention for OFS personnel involved in the Project and OEU; Oversees the cybersecurity and physical protection of OEU assets and intellectual property; Ensures safety, quality, & environmental procedures and requirements are maintained.

Orano Med Theranostics Orano Med is seeking a detail-oriented Logistics Specialist We are seeking a detail-oriented and proactive Logistics Specialist to join our fast-paced dynamic team. In this role, you will be responsible for management and oversight of all logistics and transportation operations for the Orano Med Theranostics facility in Plano, TX. Key Responsibilities Oversee all incoming/outgoing shipping activities for the Plano, TX site including providing applicable support to the Warehouse and Shipping Attendant Develop and implement logistics strategies and procedures to enhance operational efficiency Collaborate with internal teams to align logistics operations with overall business objectives. Ensure a timely and cost-efficient delivery of a variety of packages/shipments, to include: Clinical doses Raw materials Lab supplies R&D samples Empty Type A package returns Used generator returns for recycling Manage vendor relationships and contracts with selected couriers Facilitate site and process audits/inspections for all shipping activities Formulate audit and inspection responses Coordinate audit and inspection activities with vendors Manage FedEx platform and other relevant accounts for Plano, TX facility Coordinate deliveries with our carriers, recipients and Plano Team (Clinical Supply, GMP, Quality and R&D). Validate best delivery option for each shipment based on pre-determined criteria Confirm delivery option selection with appropriate teams Create bookings within courier platforms Reconcile invoices with booking estimates Act as primary shipper and consignee for hazardous materials and international shipments Prepare and manage logistics documents, correspond with carriers to ensure accuracy and compliance with all relevant regulations and industry standards Manage customs clearance process for international shipments Operate as primary contact for all shipping communications, including emergency response Communicate with carriers to resolve any issues or delays that arise during the logistics process Schedule work hours around clinical shipments to provide on-time support Generate and maintain site shipping records and logs to ensure traceability Manage inventory of Type A packages and shipping supplies. Maintain accurate records. Support Radiation Safety Officer for incoming/outgoing radioactive material shipments and maintaining inventory 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.

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

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  

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 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.

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.

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.

We are seeking a Configuration Management (CM) Engineer to join the Systems Engineering Group supporting one of the largest and most complex infrastructure projects in the United States. The CM Engineer will be responsible for establishing, implementing, and maintaining robust configuration management processes to ensure technical consistency, design traceability, and controlled evolution of system baselines across the project lifecycle. This role is critical to maintaining the integrity of engineering information and ensuring alignment between design, procurement, construction, and commissioning organizations. The successful candidate will collaborate across engineering disciplines, document control, quality assurance, and project management to ensure all technical changes are properly reviewed, approved, and recorded. Key Responsibilities Develop, implement, and maintain the project’s Configuration Management Plan and associated procedures. Establish and manage the Configuration Management database (CMDB) or equivalent tool for tracking baselines, revisions, and change status. Define and maintain system and subsystem baselines, including functional, allocated, and as-built configurations. Administer the Engineering Change Control process with the Engineering Prime Contractor (EPC), ensuring timely review, approval, and documentation of design and configuration changes, including alignment of configuration information between Owner and EPC. Work closely with Systems Engineering, Design Engineering, Procurement, Construction, and Operations to ensure technical alignment and configuration traceability. Support interface management and ensure consistent application of CM processes across all interfacing systems and organizations. Support the EPC with all configuration documentation (drawings, specifications, BOMs, design inputs/outputs) is properly controlled and versioned. Provide CM metrics, reports, and dashboards to project leadership. Participate in audits and verifications to confirm configuration status and compliance. Support readiness for system verification, validation, and commissioning by ensuring complete and accurate configuration records.