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Orano Med is seeking a Systems Administrator - Cloud to administer, monitor, and provide maintenance to the Firm's cloud based and internally hosted systems, to include O365/Azure. The employee will ensure that our systems are available, secure, and have documented and supported policies, procedures, and guidelines as directed. Tasks for the Systems Administrator may include but are not limited to: Maintain the highest level of operational standards for cloud technologies while executing best practices in operations and ongoing maintenance. Maintain plans and procedures for administration of the cloud based and on-prem systems. Maintain O365 environment to include Azure AD, Intune, Exchange Online, Teams, and OneDrive. Respond to tickets from the Service Desk that require Infrastructure support and follow appropriate ticketing procedures. Adhere to and follow Change Management Policy and procedures. Manage and complete onboarding process of new employees. Assist in management and deployment of end user and server patches and updates, including research of operational effects of the same prior to deployment Assist with data center operations, procedures and control mechanisms, documenting key controls such as physical and remote access. Receive and respond to system notifications such as Security, Compliance, or Performance notices, and take appropriate actions to remediate any problems that may occur. Test redundancy system and backup integrity as well as recovery procedures on a regular basis. Supporting remote workers / located at other sites Assist with the documentation of all system processes and procedures to ensure standardization, and best security practices. Assist with the build and maintenance of servers in the cloud environment. Automation of internal IT processes (Microsoft Power Automate, PowerShell)

Orano Med is seeking a Facilities Maintenance Engineer for radiopharmaceutical manufacturing at ATLab Indianapolis (“ATLab IND”), a new facility for commercial-scale manufacturing of sterile therapeutic radiopharmaceuticals. The Facilities Maintenance Engineer will oversee the maintenance, optimization, and compliance of our state-of-the-art manufacturing facility. The ideal candidate will ensure that all facility systems operate efficiently, safely, and in alignment with regulatory standards pertinent to the pharmaceutical industry. Facility Maintenance & Optimization: Manage and perform preventive, corrective, and predictive maintenance on facility equipment and systems to ensure optimal performance. Assess and optimize facility layout and operational systems to enhance efficiency and safety. Regulatory Compliance: Ensure all facility operations comply with FDA cGMP regulations and other relevant standards. Develop and maintain Standard Operating Procedures (SOPs) related to facility operations. Project Management: Support projects related to facility modifications, equipment installations, and system upgrades. Safety & Environmental Stewardship: Implement and uphold safety protocols to maintain a secure working environment. Manage waste disposal and recycling systems in compliance with environmental regulations. Documentation & Reporting: Maintain accurate records of maintenance activities, inspections, and compliance reports. Prepare technical reports evaluating trends and facility performance data. Other responsibilities as needed.

Join Orano – Shaping a Sustainable Future Together About the Role We are seeking a detail-oriented Assistant General Counsel with 12+ years of experience to join our legal team in Bethesda, Maryland. This role includes lead responsibility for providing legal advice and representation on a wide range of transactional matters, including supporting the negotiation and structuring of various commercial transactions, providing strategic legal guidance on commercial agreements, government contracts, and partnerships, drafting sales contracts and vendor agreements, ensuring compliance with contractual obligations, and resolving commercial disputes. Additional responsibilities may include managing litigation, and providing legal advice and representation on regulatory compliance, administrative law, mergers and acquisitions, corporate governance, international law, nuclear energy law and policy, employment law, ethics, and fiscal law. The role will report to the General Counsel and include extensive engagement with executives and managers across the company. Core Responsibilities Legal: Draft, review, and negotiate a wide variety of commercial agreements, including for example, sales contracts, vendor agreements, partnership agreements, joint ventures, license agreements, and non-disclosure agreements. Ensure that the company’s practices comply with legal and regulatory requirements. Provide strategic legal counsel on commercial agreements, government contracts, and regulatory matters Identify and assess potential legal risks associated with commercial activities and develop strategies to mitigate those risks. Resolve disputes with customers, vendors, partners and other third parties, and manage litigation when needed Manage outside counsel when specialized expertise is required Assist with legal department initiatives, including process improvements and knowledge management

Join Orano's Nuclear Energy Team   About Orano Join our 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. Our strengths? Across the entire fuel cycle, we have extensive expertise in cutting-edge technologies, safe, high value-added products and services, and a strong capacity for innovation. Overview The Engineering Manager will lead and coordinate all engineering activities for the owner/operator organization of a nuclear uranium enrichment facility. This role requires broad, multidisciplinary engineering expertise and strong leadership skills to ensure that all engineering work is technically sound, regulatory-compliant, and aligned with the project’s safety, schedule, and budget requirements. The successful candidate will serve as the primary technical interface for internal stakeholders and project partners. The role spans conceptual design, detailed design oversight, construction support, commissioning, and facility operations planning   Key Responsibilities   • Lead and coordinate all engineering disciplines (Mechanical, Instrumentation & Controls, Electrical, Civil/Structural, HVAC) throughout the project lifecycle. • Serve as the Engineering Point of Contact for the owner organization; approve technical decisions, oversee design development, and ensure integration across systems. • Ensure engineering deliverables comply with NRC regulations, DOE expectations, and ASME/ANSI standards applicable to enrichment and nuclear facility design. • Manage interfaces with the Systems Engineering teams, licensing teams, EPC contractor(s) and equipment vendors. • Support technical reviews, risk assessments, and design verifications. • Support Integrated Safety Analysis (ISA) development and licensing documentation. • Provide input to procurement specifications and ensure equipment and systems meet design and safety requirements. • Develop and manage the engineering schedule and support budgeting for engineering resources. • Facilitate technical resolution of field issues during construction and commissioning. • Champion Configuration Management and Design Control processes.

Job Description: The Associate Director, Quality Assurance supports the Company's short- and long-term goals for maintaining Quality Systems and Compliance. 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.

Orano Med: Orano Med has developed new processes for producing high-purity lead-212, a rare radioactive isotope. Lead-212 is currently at the heart of promising research projects in nuclear medicine to develop new treatments against cancer. The innovative approach, known as targeted alpha therapy (TAT), recognizes and destroys cancer cells while limiting the impact on nearby healthy cells. Job Summary: Orano Med is seeking an Instrumentation Specialist, CQV or Sr. Instrumentation Specialist, CVQ for ATLab Indianapolis, a new, state-of-the-art facility for commercial-scale, sterile manufacturing of therapeutic radiopharmaceuticals. This position offers the opportunity to help establish a new facility with high standards for quality, volume, speed, and reliability. Job Responsibilities: Oversee IQ/OQ/PQ for new instruments Draft/review/approve documents related to CQV (SOPs, calibration certificates, IQ/OQ/PQ protocols, completed IQ/OQ/PQ reports) Equipment/service logs: establish, review, maintain URS for equipment: Assist with drafting/review/approval Responsible for a variety of cGMP and non-cGMP instruments including:Production: preparatory LC, fluid transfer, dispensing, weighing, EM QC: LC, HPGe, gamma counter, sterility, analytical balances, pipettes Hot cells: VPHP, EM, fill/finish, other sensors/controls Safety: radiation detectors for personnel, surfaces, air General: refrigerators/freezers, incubators Assist with cGMP aspects of facilities equipment/sensors/controls: hot cells/cleanrooms/HVAC, temperature/RH, particle counters, fume hoods, access control, etc. Work with instrument operators to develop robust protocols for system suitability checks for equipment Assist with vendor qualifications Top Priority: On-Time Production/Release of Product Batch Release All tasks from the Setup Phase that continue into Production Phase. Carrying out/supervising calibration procedures and equipment maintenance to ensure that instruments maintain their qualified status. Preparation of calibration certificates and data reports using appropriate Quality documentation. Ensuring that the equipment is calibrated as per specifications and industry standards. Oversee warranties, PMs, scheduled recalibration/requalification Scheduling appointments for equipment maintenance and servicing. Troubleshooting and repairing equipment and/or supervise outside contractors performing these tasks Testing repaired equipment to verify qualified status Ensuring a complete stock of backup instruments, spare parts, calibration equipment, other supplies. Expert on instrumentation: liaison to management/inspectors Write protocols for in-house calibrations/qualifications Analyze/suggest equipment upgrades and software Study industry guidelines and perform Change Controls to bring Orano Med SOPs into alignment (FDA, USP/EP, ICH, PDA, etc.) Oversee investigations to resolve deviations/OOS/recalls/complaints/FMEAs related to equipment.

About Orano Med Orano Med is at the forefront of targeted alpha therapy, developing innovative radiopharmaceuticals to address critical unmet medical needs. Our mission is to harness the power of radioactive isotopes to create breakthrough treatments that transform patient care. Position Overview We are seeking a dedicated Research Associate to join our dynamic team in our radioisotope laboratory. The ideal candidate will contribute to groundbreaking research in radiopharmaceutical development while maintaining the highest standards of safety and scientific excellence. Key Responsibilities Conduct daily operations in a radioisotope laboratory, following established safety protocols Prepare and analyze samples using specialized techniques including HPLC and iTLC Perform radioactive isotope production following strict safety guidelines and procedures Execute in vitro testing using various laboratory equipment and analytical instruments Analyze, summarize, and troubleshoot studies using established laboratory practices Effectively prioritize studies, plan work sequences, and communicate results to scientists and supervisors Actively contribute to creating and maintaining a safe workplace environment Collaborate with team members, providing guidance to ensure studies progress on schedule Assist in training new personnel as needed Maintain clean and organized laboratory spaces, equipment, and inventory Begin workday at 7:00am consistently Perform additional duties as assigned

Join Orano's Nuclear Energy Team   About Orano Join our 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. Our strengths? Across the entire fuel cycle, we have extensive expertise in cutting-edge technologies, safe, high value-added products and services, and a strong capacity for innovation. Overview We are seeking a detail-oriented Records & Document Management Specialist to join our team. This role is responsible for maintaining organized record systems, supporting license application processes, and ensuring document quality and compliance with regulatory standards, particularly for Nuclear Regulatory Commission (NRC) submissions.   Key Responsibilities   Document Management Utilize advanced MS Word processing tools to create, format, edit, and proofread documents Ensure clarity, consistency, and adherence to company standards in all documentation Update and manage document templates Manage electronic and hard copy filing systems with robust version control Maintain proper organization and security of all documents (paper and electronic) License Application Support Provide word processing and editing support to ensure license applications meet required guidelines for style and format Ensure consistency of style and format between license application sections Apply proper document marking consistent with classification and NRC guidelines Maintain documents in records management systems using established file naming conventions and structure Prepare and format documents for submission to NRC Electronic Information Exchange (EIE) System Transmit information to the NRC using electronic submission systems Records Management Maintain and organize both physical and electronic records systems Ensure all records are properly cataloged, labeled, and stored according to established protocols Provide guidance to staff on proper records management practices

Position Summary The Intern – Radiopharmaceutical Manufacturing will participate in the establishment of ATLab Indianapolis as a new commercial-scale manufacturing facility for therapeutic radiopharmaceuticals. During Summer 2024, 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. 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.

Welcome to Orano Group: Powering Tomorrow's Clean Energy Join our TN Americas 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. Our strengths? Across the entire fuel cycle, we have extensive expertise in cutting-edge technologies, safe, high value-added products and services, and a strong capacity for innovation. TN Americas, a subsidiary of Orano, is seeking an MES Administrator to support activities in our state-of-the-art fabrication facility in Kernersville, NC.  This role will have responsibility for contributing to the MES system design and implementation.  Responsible for the maintenance and support of the MES system, which defines manufacturing of our products, including process flow, traceability, manufacturing instructions, etc.  Will maintain various software applications and databases that support manufacturing and serve as liaison between customers and IT to provide support. Create documentation for software usage, maintenance, and other requirements.   MAJOR DUTIES & RESPONSIBILITIES Collaborate with cross-functional teams (Manufacturing, Fabrication Project Management, Quality Assurance, and Finance) to create goals and deliverables.  Analyze current production processes, workflows, and data collection methods. Gather and document business requirements from all key stakeholders. Work closely with MES vendor for customization and deployment phase. Hands-on system configuration and interface development. Develop training material and administer training for operators, supervisors, and managers. Develop system testing, user acceptance testing (UAT), and process validation. Monitor system performance post-implementation. Identify and implement additional MES features or enhancements that support lean manufacturing, quality control, and real-time KPIs. Reviews process to ensure compliance with company and legal regulations. 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 pay information is a guideline. Your offered salary is based upon experience, qualifications, geographic location, as well as market and business considerations. Pay Range: $80,000-$95,000

Orano Med Theranostics LLC is seeking a Senior Accountant to support day-to-day accounting functions and contribute to the growth of its U.S. operations. Reporting to the Director of Financial Operations, this role will serve as a key member of the Accounting/Finance team, working collaboratively within a dynamic, mission-driven environment. Job Responsibilities: Perform daily accounting operations, including accounts payable (AP), accounts receivable (AR), journal entries, and general ledger maintenance, including intercompany transactions. Lead and execute monthly, quarterly, and year-end close processes to ensure timely and accurate financial reporting. Assist in cash management processes, including payment processing and AR collections tracking. Support budgeting and financial planning processes by preparing schedules and variance analyses. Ensure compliance with internal controls, financial policies, and accounting standards. Review and analyze financial statements, prepare account reconciliations, and validate subledger activity with a strong focus on accuracy and completeness. Collaborate with external auditors, tax consultants, and other service providers during audits and tax filings. Assist with compliance requirements for federal, state, and local taxes, including sales and use tax, payroll tax, and related filings. Contribute to process improvement initiatives to enhance efficiency and accuracy within the accounting function.

Welcome to Orano Group! Join our TN Americas 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. Our strengths? Across the entire fuel cycle, we have extensive expertise in cutting-edge technologies, safe, high value-added products and services, and a strong capacity for innovation. TN Americas, a subsidiary of Orano, is seeking a Licensing Engineer to support activities with the U.S. Nuclear Regulatory Commission (NRC) in all matters related to licensing, regulatory oversight functions, regulatory compliance, and the licensing change process, and to support activities with the U.S. Department of Transportation (DOT) and foreign nation competent authorities for transportation-associated activities. Major Duties and Responsibilities: 10 CFR Part 71 (Part 71) certificate of compliance (CoC) renewal and/or revision application coordination. Documentation maintenance for Part 71 CoC licensing bases, including safety analysis reports. 10 CFR Part 72 (Part 72) CoC renewal and amendment application coordination. Documentation maintenance for Part 72 CoC licensing bases, including updated final safety analysis reports. Submittal coordination for responses to NRC requests for supplemental or additional information. 10 CFR 72.48 safety evaluation review and approval. Coordination of DOT competent authority certification applications and interactions. Coordination of foreign-nation competent authority certification applications and interactions. Resolution of corrective action program (CAP) reports. Working with the leadership team to develop licensing compliance positions and strategies. Serving as liaison to outside organizations and NRC inspectors on licensing matters. Preparation of licensing procedures, documents, and regulatory reports to management. Leading inter-disciplinary teams to achieve various licensing and engineering projects. 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: $150,000-170,000

The Project Manager (PM) works with members of the Global Development Team (GDT) to develop, track and report on cross-functional, integrated clinical development planning, timelines and risks. The role ensures that the program moves forward at the expected cadence and in accordance with company goals and is a key member of the GDT leadership team.  Job Responsibilities: Partner with Global Development Team (GDT) technical leads to identify key deliverables and activities to be completed, identifies dependencies, and optimizes the sequence of project activities. Manage GDT meetings including developing agendas, documenting decisions and tracking/following up on action items. Ensure cross-functional alignment through the integration of interdependent activities and through the communication of plans and timelines, with specific emphasis on critical path activities. Assist GDT technical leads with anticipating and tracking the execution of required deliverables and assists with navigating project teams through corporate governance. Build out project management tools to support internal program level anticipating, tracking and reporting. Capture project risks, develop mitigation plans and communicates project status clearly internally and externally as appliable. May include supervision of 1-2 junior project planners.

Job Description: Orano Med is seeking an HR Generalist for its Plano, TX location. This position requires applicable work experience in the radiopharmaceutical, pharmaceutical, or biotechnology industry. The ideal candidate must be hands-on with strong recruitment and sourcing experience. Under limited supervision, this role performs varied human resources activities across several HR functional areas for Orano Med Theranostics in the US. Major Duties and Responsibilities The HR Generalist will perform a variety of tasks including but not limited to: Serves as primary HR contact for managers and employees on corporate policies and procedures Implements best practices supporting Orano Med's mission Partners with Corporate HR on employee relations, investigations, and strategic programs Provides performance management guidance to line management Leads recruitment efforts, including sourcing and selection of qualified candidates Extends offers and coordinates relocation as needed Develops accountable leadership focused on employee engagement and performance Builds work relationships, morale, productivity, and retention Facilitates Performance Development and People Review processes Provides workforce planning and succession planning guidance Engages with external resources to benchmark HR best practices Liaises with Orano USA HR department on policy alignment

NO WAITING PERIOD ON BENEFITS!  Rich benefit plan, effective date-of-hire. $2,000 signing bonus, paid after 60 days of employment. Join our outstanding fabrication team in Orano’s state-of-the-art Kernersville facility!  Embark on a career in supplying the nuclear industry with specialized products proudly made here in the heart of North Carolina! Job Description Orano is seeking Experienced Welders to support the work performed in its nuclear fabrication facility in Kernersville, NC. This position offers top pay and outstanding benefits with no waiting period. Major Duties and Responsibilities Weld components using both GTAW (TIG) and GMAW (MIG) welding processes. Perform fit-up as needing in fabrication process. Work from travelers (shop routers), procedures, standards, and written and verbal instructions. Maintain traceability of all materials and processes through established procedures. Operate grinders and perform other shop fabrication tasks as needed. Maintain clean and orderly work area. Ensure proper functioning of equipment and maintain all tooling and equipment in accordance with standard shop practices. 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 pay information is a guideline. Your offered salary is based upon experience, qualifications, geographic location, as well as market and business considerations. Pay Range: $27-$31/hour

Join our team at Orano USA and contribute to building the clean energy world of tomorrow. As an intern, you'll be part of a leading international player in the nuclear industry, gaining valuable experience in cutting-edge technologies and innovative solutions across the entire fuel cycle. Under guidance from experienced professionals, the System Safety Engineering Intern will assist in various aspects of complex engineering tasks. You'll support systems engineering activities, including safety, security, cybersecurity, and reliability requirements. This internship offers exposure to multidisciplinary teams (chemical, structural/civil, mechanical, I&C, electrical, HVAC) and provides insight into major projects in the nuclear industry. Objectives: Assist in coordinating engineering work, including helping to establish and maintain requirements, overall technical solutions, and safety basis documentation. Support functional analysis and learn to document the functional allocation to systems and subsystems. Help in identifying and documenting system interfaces, gaining understanding of their importance in complex projects. Observe and participate in day-to-day operations, interacting with engineers, designers, and engineering technicians on specific project assignments. Learn about project management by supporting schedule and cost performance tracking, assisting in status report preparation, and observing how deviations are identified and recovery plans proposed. Engage in various tasks supporting planning, design, procurement, construction, commissioning, and plant operation and maintenance, as appropriate for an internship role. This internship offers a unique opportunity to gain hands-on experience in the nuclear industry while developing valuable skills in systems engineering and project management.

NO WAITING PERIOD ON BENEFITS!  Rich benefit plan, effective date-of-hire.  Join our outstanding fabrication team in Orano’s state-of-the-art Kernersville facility!  Embark on a career in supplying the nuclear industry with specialized products proudly made here in the heart of North Carolina!  Orano TN, a subsidiary of Orano, is seeking Manufacturing Tech to support TN Fabrication’s NC facility in Kernersville/Greensboro.   Major Duties and Responsibilities The Manufacturing Tech will perform a variety of fabrication tasks including but not limited to: Perform assembly, and intermediate level equipment and tooling set up. Perform intermediate level parts preparation Operate various saws, CNC cutting machines (such as laser, waterjet, plasma), and other equipment as required Perform rigging, either by assisting or leading the task, to transport parts throughout the facility Abrasively blast and/or paint product in fabrication phases or as final assemblies Follow shop travelers with minimal supervision and making accurate document entries Work flexible hours and shifts, as required, to ensure timely service Work from drawings, specifications, procedures, SWIs, electronic data, and written and verbal instructions Grind welds, blend parts, remove burrs, wire brush parts, steel stamp parts, clean parts with solvent or steam, wrap parts with plastic and/or tarps for shipment, and help load parts as required Straighten assemblies, as required, throughout various stages of fabrication Assist maintenance and other shop or office personnel in moving or handling materials, parts, equipment, furniture, or other items as required Keep work area and equipment clean and orderly Utilize the principles of Lean Manufacturing.

NO WAITING PERIOD ON BENEFITS! Rich benefit plan, effective date-of-hire. Join our outstanding fabrication team in Orano’s state-of-the-art Kernersville facility! Embark on a career in supplying the nuclear industry with specialized products proudly made here in the heart of North Carolina!   Job Description TN Americas, a subsidiary of Orano, is seeking an NDE Tech I-II to support the Quality Control/NDE work performed in its Kernersville, NC fabrication facility.  This role is key in Orano’s fabrication of storage and transportation packages for nuclear materials projects. The NDE Tech will perform a variety of quality inspections and NDE tasks including but not limited to: In-process NDE including visual examination (VT), penetrant examination (PT), bubble leak examination (BT), and ultrasonic thickness (UTT) Completing documentation accurately and effectively In-process mechanical inspections, including dimensional and testing activities Interface with customer oversight representatives Support manufacturing/production schedules Assist supervisor with other duties. Orano strives to provide a total compensation package that brings value to our employees. We offer highly competitive health and wellness programs, 401(k) contributions, and industry-leading paid time off.