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Job Description Grow your career while reshaping the world. Location: UK. AtkinsRéalis Building Design Practice are looking for an experienced, motivated Senior/Principal Vertical Transportation (VT), lift and escalators Design Engineer looking to develop their career in a positive environment and join our team where talent is encouraged and growth opportunities unrivalled. This flexible and agile role can be based in one of our UK Offices to suit the successful candidate and presents the opportunity to join a national delivery team and work with designers across the UK and internationally through our Global Design Centre. This opportunity will involve working as part of a national practice of Building Design professionals delivering Vertical Transportation, lift and escalators engineering design solutions to clients across the UK. The Building Design practice work on projects across all our focus markets, including Aviation, Cities &amp; Development, Defence, Education, Energy, Government and Transportation. The opportunity will require candidates to be able to work as part of an international team and single-handedly, under their own initiative in a client-facing role, as well as being involved in the day-to-day design and management of their varied portfolio of projects. It is an exciting opportunity for an experienced design engineer to further develop their career within a prominent building design consultancy. Our focus is on developing our staff to realise their full potential, with development plans geared to personal needs and abilities. This role will allow development of existing technical skills on unique, high profile, signature projects as well as providing potential to expand digital skills and become a prominent expert in your specialist knowledge area. Our Practice is committed to developing our ways of working using emerging Digital Technology and the global reach offered by an organisation of our size and reach. Our ideal individual will bring strong technical skills to the role, as well as an enquiring mind able to contribute to the growth of our digital practice, and the ability to inspire and manage large and diverse delivery teams, locally and remotely. The breadth and interest in the projects across AtkinsRéalis are extremely interesting and allows a crossover between different solutions. We invite you to bring your enthusiasm and expertise into play as you help develop a team of specialists in the field of lifts and escalators to contribute to innovative and high-quality design solutions. To succeed in this role, you must have technical skills and experience with a detailed knowledge of applicable Standards and Regulations. A customer focus to deliver what the client expects plus a bit more when necessary. Your purpose: <ul><li>Lead the design and specification of vertical transportation systems for commercial, residential, and mixed-use developments.</li><li>Prepare technical reports, design documentation, and tender packages.</li><li>Coordinate with architects, structural engineers, and other disciplines to integrate VT systems into building designs.</li><li>Conduct feasibility studies, traffic analysis, and performance assessments.</li><li>Conduct site surveys and commissioning experience. </li><li>Review and approve contractor submissions, shop drawings, and equipment selections.</li><li>Provide technical guidance and mentorship to junior engineers.</li><li>Liaise with clients, suppliers, and regulatory bodies to ensure project objectives are met.</li><li>Stay updated with relevant codes, standards, and emerging technologies in vertical transportation.</li></ul> What you can bring: <ul><li>Bachelor's or Master's degree in Mechanical Engineering or Building Services Engineering / NVQ Level 3 Lift &amp; Escalator.</li><li>Proven experience in vertical transportation design, ideally across multiple building types.</li><li>Strong understanding of lift and escalator technologies, control systems, and safety standards.</li><li>Familiarity with relevant codes and standards (e.g., EN 81, BS 5656, ISO standards).</li><li>Experience in traffic simulation and analysis tools (e.g., Elevate, Liftdesigner).</li><li>Excellent communication and stakeholder management skills.</li><li>Chartered Engineer status (or working towards) is desirable for Principal level.</li><li>Experience working in a consultancy environment and ability to manage multiple projects and deadlines.</li><li>Strong problem-solving and analytical skills and passion for innovation and continuous improvement.</li></ul> Why work for AtkinsRéalis? We're ranked as one of LinkedIn's Top 25 Companies, where UK professionals want to work and stay once, they join. We've also made the Times Top 50 employers for women. Our Infrastructure team uses innovation, new approaches and the power of data to help our clients deliver end-to-end projects and programmes for essential future infrastructure. And as the work becomes ever more complex, our employees continue to challenge the status quo. We're committed to engineering better for people and our planet, from our global Engineering Net-Zero programme to creating social value through EDAROTH community housing. We're proud of our active employee networks creating awareness and allyship for our under-represented groups. Not to mention programmes supporting communities outside AtkinsRéalis, including schools, charities, ex-forces and professionals returning after career breaks. Security clearance: This role may require security clearance and offers of employment will be dependent on obtaining the relevant level of clearance. If this is necessary, it will be discussed with you at interview. The vetting process is delivered by United Kingdom Security Vetting (UKSV) and may require candidates to provide proof of residency in the UK of 5 years or longer. If applying to this role please do not make reference to (in conversation) or include in your application or CV, details of any current or previously held security clearance. We are committed to promoting a diverse and inclusive community - a place where we can all be ourselves, thrive and develop. To help embed inclusion for all, from day one, we offer a range of family friendly, inclusive employment policies, flexible working arrangements and employee networks to support staff from different backgrounds. As an Equal Opportunities Employer, we value applications from all backgrounds, cultures and ability. #LI-INFRASTRUCTURE | #LI-UK#LI-UKI Worker Type Employee Job Type Regular At AtkinsRéalis, we seek to hire individuals with diverse characteristics, backgrounds and perspectives. We strongly believe that world-class talent makes no distinctions based on gender, ethnic or national origin, sexual identity and orientation, age, religion or disability, but enriches itself through these differences.

Senior / Principal Design Engineer - Vertical Transportation Systems (Lifts and Escalators)

If you are a current Jazz employee please apply via the Internal Career site.
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to 
transform the lives of patients and their families. We are dedicated to developing 
life-changing medicines for people with serious diseases — often with limited or no 
therapeutic options. We have a diverse portfolio of marketed medicines, including leading 
therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. 
Our patient-focused and science-driven approach powers pioneering research and development 
advancements across our robust pipeline of innovative therapeutics in oncology and 
neuroscience. Jazz is headquartered in Dublin, Ireland with research and development 
laboratories, manufacturing facilities and employees in multiple countries committed to 
serving patients worldwide. Please visit
<a href="https://www.jazzpharmaceuticals.com" target="_blank">www.jazzpharmaceuticals.com</a>
for more information.
 Brief Description: The Principal, AI Data Scientist will be responsible for supporting the implementation of innovative, complex and transformative AI/ML/GenAI solutions across the areas of Clinical Trial Execution and Digital Healthcare across Jazz Research and Development.Essential Functions<ul><li>Support the development and implementation of AI/ML/GenAI solutions to optimize clinical trial operations, including such areas as patient recruitment, patient retention, real-time data monitoring and automated data collection system build.</li><li>Support the development and implementation GenAI applications for automated clinical trial documentation generation including such areas medical reports, clinical study reports, protocols and patient narratives.</li><li>Support the development and implementation of Digital Healthcare applications for medical and scientific tools, RWE new ways of generating real data, patients’ engagement.</li><li>Support the design and develop predictive models and generative AI solutions using diverse healthcare data sources, including clinical trials data, electronic health records, wearable devices, patient-reported outcomes, HEOR data, phase IV studies.</li><li>Collaborate with cross-functional teams including clinical operations, clinical development, data science and global medical &amp; scientific affairs, RWE and patients working groups to tackle business challenges and bring value of AI-driven solutions.</li><li>Ensuring compliance with regulatory requirements and data privacy standards.</li><li>Facilitate knowledge sharing and exchange within Jazz Data Science and across Jazz Research and Development.</li></ul>Required Knowledge, Skills and Abilities <ul><li>Strong programming skills in Python, R, or similar languages, with experience in modern ML frameworks (PyTorch, TensorFlow).</li><li>Demonstrated experience with generative AI technologies, including LLM architectures and frameworks.</li><li>Knowledge/experience with digital healthcare tools design and development</li><li>Experience with natural language processing and generative AI for medical text analysis, generation, and interpretation.</li><li>Demonstrated ability to build relationships with stakeholders and subject matter experts.</li><li>Familiarity with high compute cloud-based platforms and services, in particular AWS.</li><li>Familiarity with code version control and MLOps deployment approaches.</li><li>Ability to understand healthcare challenges and adapt accordingly the AI solutions.</li><li>Cross-functions high adaptability to meet cross organization goals.</li></ul>Required/Preferred Education<ul><li>Advanced degree (MS or PhD) in Data Science, Computer Science, Biostatistics, or related field</li><li>3 – 5 years of related professional experience, with 1+ years of experience applying AI/ML techniques to healthcare or clinical research data.</li><li>Experience in healthcare/AI implementation in healthcare field is a plus.</li><li>Knowledge in digital healthcare tools design and development</li></ul>Description of Physical Demands<ul><li>Occasional mobility within office environment</li><li>Routinely sitting for extended periods of time</li><li>Constantly operating a computer, printer, telephone and other similar office machinery</li></ul> Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: <a href="https://careers.jazzpharma.com/benefits.html" target="_blank">https://careers.jazzpharma.com/benefits.html</a>.

Principal, AI Data Scientist (Remote)

If you are a current Jazz employee please apply via the Internal Career site.
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to 
transform the lives of patients and their families. We are dedicated to developing 
life-changing medicines for people with serious diseases — often with limited or no 
therapeutic options. We have a diverse portfolio of marketed medicines, including leading 
therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. 
Our patient-focused and science-driven approach powers pioneering research and development 
advancements across our robust pipeline of innovative therapeutics in oncology and 
neuroscience. Jazz is headquartered in Dublin, Ireland with research and development 
laboratories, manufacturing facilities and employees in multiple countries committed to 
serving patients worldwide. Please visit
<a href="https://www.jazzpharmaceuticals.com" target="_blank">www.jazzpharmaceuticals.com</a>
for more information.
 The Principal, AI Data Scientist will be responsible for supporting the implementation of innovative, complex and transformative AI/ML/GenAI solutions across the areas of Clinical Trial Execution and Digital Healthcare across Jazz Research and Development.Essential Functions<ul><li>Support the development and implementation of AI/ML/GenAI solutions to optimize clinical trial operations, including such areas as patient recruitment, patient retention, real-time data monitoring and automated data collection system build.</li><li>Support the development and implementation GenAI applications for automated clinical trial documentation generation including such areas medical reports, clinical study reports, protocols and patient narratives.</li><li>Support the development and implementation of Digital Healthcare applications for medical and scientific tools, RWE new ways of generating real data, patients’ engagement.</li><li>Support the esign and develop predictive models and generative AI solutions using diverse healthcare data sources, including clinical trials data, electronic health records, wearable devices, patient-reported outcomes, HEOR data, phase IV studies.</li><li>Collaborate with cross-functional teams including clinical operations, clinical development, data science and global medical &amp; scientific affairs, RWE and patients working groups to tackle business challenges and bring value of AI-driven solutions.</li><li>Ensuring compliance with regulatory requirements and data privacy standards.</li><li>Facilitate knowledge sharing and exchange within Jazz Data Science and across Jazz Research and Development.</li></ul>Required Knowledge, Skills and Abilities <ul><li>Strong programming skills in Python, R, or similar languages, with experience in modern ML frameworks (PyTorch, TensorFlow).</li><li>Demonstrated experience with generative AI technologies, including LLM architectures and frameworks.</li><li>Knowledge/experience with digital healthcare tools design and development</li><li>Experience with natural language processing and generative AI for medical text analysis, generation, and interpretation.</li><li>Demonstrated ability to build relationships with stakeholders and subject matter experts.</li><li>Familiarity with high compute cloud-based platforms and services, in particular AWS.</li><li>Familiarity with code version control and MLOps deployment approaches.</li><li>Ability to understand healthcare challenges and adapt accordingly the AI solutions.</li><li>Cross-functions high adaptability to meet cross organization goals.</li></ul>Required/Preferred Education<ul><li>Advanced degree (MS or PhD) in Data Science, Computer Science, Biostatistics, or related field</li><li>3 – 5 years of related professional experience, with 1+ years of experience applying AI/ML techniques to healthcare or clinical research data.</li><li>Experience in healthcare/AI implementation in healthcare field is a plus.</li><li>Knowledge of digital healthcare tools design and development</li></ul>Description of Physical Demands<ul><li>Occasional mobility within office environment</li><li>Routinely sitting for extended periods of time</li><li>Constantly operating a computer, printer, telephone and other similar office machinery</li></ul> Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: <a href="https://careers.jazzpharma.com/benefits.html" target="_blank">https://careers.jazzpharma.com/benefits.html</a>.

Principal, AI Data Scientist-2

If you are a current Jazz employee please apply via the Internal Career site.
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to 
transform the lives of patients and their families. We are dedicated to developing 
life-changing medicines for people with serious diseases — often with limited or no 
therapeutic options. We have a diverse portfolio of marketed medicines, including leading 
therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. 
Our patient-focused and science-driven approach powers pioneering research and development 
advancements across our robust pipeline of innovative therapeutics in oncology and 
neuroscience. Jazz is headquartered in Dublin, Ireland with research and development 
laboratories, manufacturing facilities and employees in multiple countries committed to 
serving patients worldwide. Please visit
<a href="https://www.jazzpharmaceuticals.com" target="_blank">www.jazzpharmaceuticals.com</a>
for more information.
 Brief Description:The Senior Analyst of Medical Affairs (Medical Education Grants) will be an integral member of the Medical Affairs, Medical Education Grant team. This role is essential for enhancing efficiency and effectiveness of the department’s operational and management of Independent Medical Education grant requests from external organizations.Essential Functions<ul><li>Monitor the Educational Grant Management System and perform initial review of grant requests for completeness and alignment to industry and company guidelines</li><li>Partner with Grants Manager to track routed requests against the budget to ensure approvals do not exceed the target forecast</li><li>Process grant requests, to include communication of grant decisions to internal and external parties and issuing of payment to requestors</li><li>Maintain a schedule of supported educational events across all Neuroscience molecules</li><li>Track outcomes from supported programs</li><li>Gather and assist analyze performance metrics under Grant Managers’ oversight and communicate the results to stakeholders within the organization as needed.</li><li>Prepare presentations for use by Grants Manager and other internal departments as needed</li><li>Respond to reported problems and work with a diverse team of internal and external stakeholders to identify resolutions</li><li>Schedule monthly EGRC meetings, distribute review materials to the team prior to the meeting, and prepare presentation materials</li><li>Identify potential process improvements related to the grant workflow</li><li>Update documentation related to IME grant processes and workflow diagrams to ensure business continuity and aid in continuous improvement efforts</li><li>Communicate regularly with grant requestors regarding status, payment, program materials and outcomes of supported activities</li><li>Analyze operational processes and systems and establish best practices</li><li>Participate in professional meetings to evaluate the impact that regulatory and policy decisions have on IME grants</li><li>Partner with IME Director on special projects</li></ul>Required Knowledge, Skills, and Abilities <ul><li>Pharmaceutical industry and/or agency/medical education company experience is required</li><li>Experience working with Microsoft Office, including Excel, PowerPoint, Outlook and Word is required</li><li>Experience working with Pivot Tables, Macros and/or Visual Basic for Applications is preferred</li><li>Experience working with publication software (e.g., Microsoft Publisher, Adobe InDesign) is desired</li><li>Knowledge/understanding of FDA and regulatory guidelines for industry support of medical education events (e.g., PhRMA guidelines, OIG, AMA, ACCME, Sunshine Act) is desired</li><li>Knowledge of CME/CE outcomes assessments (e.g., MOOREs, TELMs) is desired</li><li>Experience working with reporting solutions (e.g., Izenda, SmartSheets) is desired</li><li>Experience working with a request management or customer management system is desired (e.g., CyberGrants, Vision Tracker, CRM systems)</li></ul>Required/Preferred Education and Licenses<ul><li>Relevant degree, direct experience working in independent medical education grants or a mix of both </li></ul> Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. FOR US BASED CANDIDATES ONLYJazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is: $102,400.00 - $153,600.00Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis.At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: <a href="https://careers.jazzpharma.com/benefits.html" target="_blank">https://careers.jazzpharma.com/benefits.html</a>.

Senior Analyst, Global Medical Affairs, Independent Medical Education Grants

If you are a current Jazz employee please apply via the Internal Career site.
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to 
transform the lives of patients and their families. We are dedicated to developing 
life-changing medicines for people with serious diseases — often with limited or no 
therapeutic options. We have a diverse portfolio of marketed medicines, including leading 
therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. 
Our patient-focused and science-driven approach powers pioneering research and development 
advancements across our robust pipeline of innovative therapeutics in oncology and 
neuroscience. Jazz is headquartered in Dublin, Ireland with research and development 
laboratories, manufacturing facilities and employees in multiple countries committed to 
serving patients worldwide. Please visit
<a href="https://www.jazzpharmaceuticals.com" target="_blank">www.jazzpharmaceuticals.com</a>
for more information.
 Brief Description: This position is responsible for leading efficient, innovative, clinical pharmacology and/or PK/PD studies from phase 1 to phase 4 through working with cross-functional team members.Essential Job Functions:Job Responsibilities<ul><li>Development of the clinical pharmacology strategy of multiple programs spanning from candidate nomination for GLP toxicity studies through phase 4</li><li>Support clinical study protocol (phase 1-4) development, PKPD data analysis/interpretation, and study report</li><li>Serve as the clinical pharmacology Lead at cross function teams, and responsible for the dose selection and rationale in phase 1 studies and contribute to dose selections in clinical studies beyond phase 1</li><li>Work with the pharmacometrics lead and relevant cross-function teams to plan and support PKPD modeling for internal or regulatory decision makings</li><li>Contribute to the preparation of relevant sections of regulatory submissions including IND, and NDA/BLA documents</li><li>Address queries from regulatory agencies during reviews and inspections&nbsp;</li><li>Identify and manage consultants and vendors supporting clinical pharmacology studies</li><li>Contribute to the timely publication and/or presentation of clinical pharmacology and pharmacometrics data</li></ul>Required Knowledge, Skills, and Abilities<ul><li>PhD or MD with significant years of experience in clinical pharmacokinetic and pharmacokinetic-pharmacodynamic studies and data analysis/interpretations</li><li>Strong understanding of clinical pharmacology and pharmacometrics principles and the drug development process</li><li>Good working knowledge of software for PK/PD analysis (e.g. Phoenix WinNonlin, R, ADAPT and NONMEM) </li><li>Ability to work both independently and on strong cross functional teams</li><li>Experience in regulatory submissions and agency interactions related to INDs, CTDs, NDAs or BLAs</li><li>Excellent written and oral communication skills including good presentation skills</li><li>Collaborative and flexible in personal interactions at all levels of the company</li></ul>Jazz Pharmaceuticals is an equal opportunity/affirmative action employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law. The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: <a href="https://careers.jazzpharma.com/benefits.html" target="_blank">https://careers.jazzpharma.com/benefits.html</a>.

Director, Clinical Pharmacology & Pharmacometrics (Remote)

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Principal, AI Data Scientist-1 (Remote)

Title: Principal Electrical Engineer KBR is a global provider of differentiated, professional services and technologies delivered across a wide government, defense and industrial base. Drawing from its rich 100-year history and culture of innovation and mission focus, KBR creates sustainable value by combining engineering, technical and scientific expertise with its full life cycle capabilities to help our clients meet their most pressing challenges today and into the future. We deliver science, technology and engineering solutions to governments and companies around the world. KBR employs approximately 37,000 people worldwide with customers in more than 80 countries and operations in over 29 countries. KBR is proud to work with its customers across the globe to provide technology, value-added services, and long-term operations and maintenance services to ensure consistent delivery with predictable results. At KBR, We Deliver. Job Description: As part of the electrical engineering team, you will be involved in the design, specification and services relating to Electrical engineering for projects relating to energy transition. This may be a conceptual study or front-end engineering design (FEED) or an EPC / detailed design execution involving, the procurement of all equipment and detailed drawings for the construction and commissioning of an entire facility. There will be a focus within the design on cost, schedule, safety, reliability, and quality at all stages of the projects. You will be responsible for study, design, specification and services related to electrical systems including power generation, transmission and distribution, power systems performance and control, switchgear, earthing systems, lightning protection systems, heat tracing etc. depending on the project phase. You will perform assignments with minimal supervision using your knowledge of engineering principles. You will be responsible for checking your own and others work within the team and approving deliverables for issue. Roles &amp; Responsibilities: <ul><li>Taking an active role in the design of electrical system to required specifications, focusing on cost, schedule, safety, reliability, and quality</li><li>Creating and interpreting philosophies, design specifications, data sheets, schematics and layout drawings for oil and gas onshore and offshore installations</li><li>Acting as a technical expert within a project</li><li>Assist in the supervising or leading of a discipline team and providing their technical direction</li><li>Direction and coaching of other members of the team</li><li>Responsible for resolving and providing solutions to highly complex technical problems encountered on Projects</li><li>Involved in projects from concept to detailed design through to construction, testing and handover</li><li>Working in a multi-disciplinary project team, which is likely to include engineers from other specialism's including mechanical, structural, civil and instrumentation, liaising with clients, vendors and contractors</li></ul> Skills &amp; Experience: <ul><li>Concept / FEED / EPC Electrical Engineering experience (Energy Transition Projects)</li><li>Interpreting technical drawings and / or creating or checking schematics or other electrical drawings.</li><li>Managing electrical interfaces between packages including GTGs and Switchgear</li><li>Vendor package management (electrical and mechanical packages)</li><li>Good working knowledge of Electrical design at 132kV to 400V</li><li>Working knowledge of applicable industry codes and standards</li><li>User of ETAP software or equivalent</li></ul> Educational Experience: • Bachelors/Master degree in an Electrical Engineering subject with relevant industry experience. • Chartered engineer status with a relevant professional body preferred. KBR COMPANY INFORMATION When you become part of the KBR team, your opportunities are endless. Through collaboration with our customers, we're defining tomorrow's challenges, then providing the solutions and services to overcome those challenges, always maintaining our commitment to total safety and reliability. At KBR, we partner with government and industry clients to provide purposeful and comprehensive solutions with an emphasis on efficiency and safety. With a full portfolio of services, proprietary technologies and expertise, our employees are ready to handle projects and missions throughout their entire lifecycle, from planning and design to sustainability and maintenance. Whether at the bottom of the ocean or in outer space, our clients trust us to deliver the impossible on a daily basis. Working at KBR means being rewarded for your contributions. In addition to competitive benefits and professional development, our people are empowered to use all their potential, creating meaningful change for themselves and our clients. We attract the best minds in the world because our expertise thrives on creativity, resourcefulness and collaboration. That is how we supply our clients with cutting-edge solutions and services. As the needs of the world change, we're ready to respond and guide the way forward with strategic, sustainable, and technological advancements grounded in more than a century of practical application and execution. #LI-PS1

2,056 Jobs in Weybridge, UK