account manager

area sales manager

contract administrator

senior commercial manager

environmental manager

regulatory affairs manager

Siemens Energy

<div><div>A Snapshot of Your Day: As the Government Affairs Manager, you will develop and implement a comprehensive government affairs strategy in collaboration with the country MD, ensuring alignment with Siemens Energy&rsquo;s objectives. You will monitor and analyze legislative developments, geopolitical trends, and stakeholder dynamics, while fostering relationships with key government representatives and industry associations to enhance our market position and reputation.</div><div></div><div><br>
How You&rsquo;ll Make an Impact:</div><div></div><div><br>
<ul><li>
Develop, monitor, and implement an annual government affairs strategy aligned with the country strategy.</li><li>
Track and respond to key country and BA issues requiring government affairs mitigation and support.</li><li>
Analyze and influence policy, legislative, and regulatory developments impacting Siemens Energy&rsquo;s operations.</li><li>
Identify engagement platforms to drive advocacy and enhance Siemens Energy&rsquo;s reputation in decision-making processes.</li><li>
Prepare executive briefing materials and reports in coordination with relevant stakeholders.</li><li>
Represent Siemens Energy at industry events and meetings with government officials.</li></ul></div><div></div><div><br>
What You&rsquo;ll Bring:</div><div></div><div><br>
<ul><li>
Bachelor&rsquo;s degree in Political Science, Public Administration, Business, or a related field; Master&rsquo;s degree preferred.</li><li>
Minimum of 15 years of experience in government affairs or public policy within the energy sector.</li><li>
Strong understanding of policy, legislative, and regulatory processes.</li><li>
Excellent communication, negotiation, and interpersonal skills.</li><li>
Proven ability to build and maintain relationships with government officials and stakeholders.</li><li>
Strategic thinker with the ability to analyze complex issues and develop effective advocacy strategies.</li></ul></div><div><br>
<p></p><br>
<p>Our <i>Corporate Functions</i> are essential in driving the company's strategic initiatives and ensuring operational excellence across various departments, business areas, and regions. These roles support our vision to become the most valued energy technology company in the world. As part of our team, you contribute to our vision by shaping the global energy transition, partnering with our internal and external stakeholders, and conducting business responsibly and in compliance with legal requirements and regulations.</p><p></p><p><b><br>
Who is Siemens Energy?</b></p>
<p><b>At Siemens Energy, we are more than just an energy technology company. With ~100,000 dedicated employees in more than 90 countries, we develop the energy systems of the future, ensuring that the growing energy demand of the global community is met reliably and sustainably. The technologies created in our research departments and factories drive the energy transition and provide the base for one sixth of the world's electricity generation.
</b></p><p><b>Our global team is committed to making sustainable, reliable, and affordable energy a reality by pushing the boundaries of what is possible. We uphold a 150-year legacy of innovation that encourages our search for people who will support our focus on decarbonization, new technologies, and energy transformation.
</b></p><p><b>Find out how you can make a difference at Siemens Energy: </b><b>https://www.siemens-energy.com/employeevideo</b></p>
<p><b>Our Commitment to Diversity</b></p>
<p><b>Lucky for us, we are not all the same. Through diversity we generate power. We run on inclusion and our combined creative energy is fueled by over 130 nationalities. Siemens Energy celebrates character &ndash; no matter what ethnic background, gender, age, religion, identity, or disability. We energize society, all of society, and we do not discriminate based on our differences.</b></p>
<p><b>Rewards/Benefits</b></p>
<ul><li><b>Competitive Salary Package</b></li>
<li><b>Targeted Bonus</b></li>
<li><b>Opportunities to work on a variety of innovative projects</b></li>
</ul>
<p><b>https://jobs.siemens-energy.com/jobs</b></p>
<p><b>#LI-AF1</b></p></div></div>

Government Affairs Manager- Siemens Energy, Riyadh KSA

Johnson & Johnson

<div><p>At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com</p><p><b>
Job Function:
</b></p>Regulatory Affairs Group<p><b>
Job Sub Function:
</b></p>Regulatory Product Submissions and Registration<p><b>
Job Category:</b></p>
Professional<p><b>
All Job Posting Locations:</b></p>
Riyadh, Saudi Arabia<p><b>
Job Description:</b></p><p><b>
About MedTech</b></p><p>
Fueled by innovation at the intersection of biology and technology, we&rsquo;re developing the next generation of smarter, less invasive, more personalized treatments.</p><p>
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech</p><p><b>
REGULATORY AFFAIRS SPECIALIST (MEDICAL DEVICES)</b></p><p><b>
Location: Riyadh</b></p><p><b>
Contract: full-time</b></p><p><b>
Purpose:</b></p><p>
The main task of a Regulatory Affairs specialist in Johnson &amp; Johnson is Launching of Medical Device Products in Saudi Arabia Market in compliance with the Regulatory registration &amp; importation guidance.</p><p><b>
You will be responsible for:</b></p><ul><li>
Preparing, compiling and submission of registration/ re-registration products files in addition to variation submission on time directly in Saudi Arabia or through J&amp;J distributors when applicable</li><li>
SFDA meetings</li><li>
Clearance support to distributors</li><li>
Updating the regulatory tracking systems</li><li>
Having the renewed certificates &amp; re-registration licenses of expired ones on time</li><li>
Responding to Change Impact Assessments before due dates</li><li>
Doing Copy Review process for promotional materials on time upon request</li><li>
Lift all regulatory restrictions for products that can be shipped to Saudi Arabia</li><li>
Tender support to commercial teams &amp; distributors</li></ul><p><b>
Qualifications / Requirements:</b></p><ul><li>
Education: Bachelor&rsquo;s (B.Sc.) degree of Biomedical engineering or Sciences</li><li>
Minimum 2 years of Regulatory Affairs experience withing Medical Devices industry</li><li>
Language: English &amp; Arabic (fluent)</li><li>
Time Management</li><li>
Very good presentation &amp; communication skills</li><li>
Sense of urgency, attention to details, creative problem-solving</li><li>
Collaboration &amp; teamwork</li><li>
Self-motivation, ability to work under stress</li><li>
Involvement in Regional Projects</li><li>
Saudi national</li></ul></div>

Regulatory Affairs Specialist (medical devices)

AstraZeneca

<div><p><b>JOB TITLE</b></p><p></p><p><b>
Regulatory Affairs Lead</b></p><p><b><br>
ABOUT ASTRAZENECA</b></p><p>
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world&rsquo;s most serious diseases. But we&rsquo;re more than one of the world&rsquo;s leading pharmaceutical companies.</p><p></p><p><b>
ROLE SUMMARY
</b></p><p></p><p>The Regulatory Affairs Lead is responsible for driving regulatory strategies and managing submissions across the product lifecycle to ensure compliance with local and global requirements. The role provides expert advice on processes and documentation, proactively manages regulatory risks, and partners with health authorities and internal stakeholders to enable timely patient access to innovative medicines.</p><p></p><p><b>
What you&rsquo;ll do</b></p><p><b>
Regulatory Strategy &amp; Submissions</b></p><ul><li>
Lead submission management and cross-functional teams for complex global regulatory applications, ensuring compliance with AstraZeneca&rsquo;s submission-ready standards.</li><li>
Provide regulatory expertise and strategic input to product and project teams, anticipating Health Authority requirements and guiding submissions-related activities.</li><li>
Identify potential regulatory risks to global and regional operational plans, proposing mitigation strategies.</li><li>
Implement and oversee strategies that improve the quality, efficiency, and timeliness of submissions.</li><li>
Manage processes related to product licenses, registrations, and post-marketing requirements, including labeling, safety reporting, inspections, and audits.</li><li>
Act as the primary regulatory contact with key authorities (e.g., SFDA, GHC) and ensure timely updates to global systems on regulatory guidelines, decrees, and communications.</li></ul><p><b>
Business Partnering &amp; Country RA Agenda</b></p><ul><li>
Serve as the regulatory contact for the Country Head and Business Unit Directors (BUDs).</li><li>
Conduct regular meetings with local agents&rsquo; regulatory teams to align on outstanding activities and ensure smooth execution.</li><li>
Foster alignment across therapy area RA managers, local agents, and global stakeholders on regulatory priorities.</li><li>
Represent AstraZeneca&rsquo;s regulatory interests in official engagements with authorities and industry forums.</li></ul><p></p><p><b>
Leadership &amp; People Development</b></p><ul><li>
Manage and develop a small team of regulatory professionals (1&ndash;2 direct reports), setting clear objectives, coaching, and providing growth opportunities.</li><li>
Promote a culture of collaboration, creativity, and courageous leadership across teams.</li><li>
Lead or participate in critical projects, ensuring regulatory business needs are integrated into AZ&rsquo;s systems, processes, and standards.</li></ul><p></p><p><b>
External Engagement &amp; Business Awareness</b></p><ul><li>
Build and maintain strong relationships with Regulatory Health Authorities, industry representatives, and key external partners.</li><li>
Monitor regulatory, policy, and industry dynamics, proactively advising internal stakeholders on potential impacts.</li><li>
Support business development activities, including proposals, reports, costing, and budgets, ensuring alignment with corporate strategy.</li></ul><p></p><p><b>
Governance &amp; Compliance</b></p><ul><li>
Ensure all regulatory activities adhere to AstraZeneca&rsquo;s Code of Ethics, corporate policies, and local legislation.</li><li>
Timely reporting of adverse events, compliance risks, conflicts of interest, and health/environment-related incidents.</li><li>
Provide regulatory input for audits, inspections, recalls, and related communications to minimize compliance risks.</li></ul><p></p><p><b>
Only applications in KSA will be considered.</b></p><p><b>
Essential for the role</b></p><ul><li>
Saudi National</li><li>
Higher education in pharmaceuticals, medicine, or biotechnology.</li><li>
Minimum 9 years&rsquo; experience in regulatory affairs (drug development, product approval/launch, line extension, license maintenance, or Health Authority experience), including at least 5 years in a multinational environment with proven contributions.</li><li>
Strong knowledge of local and international regulatory standards, requirements, and industry practices.</li><li>
Demonstrated ability to manage pivotal projects and resource requirements.</li><li>
Excellent collaboration and teamworking skills across global functions.</li><li>
Proven people management capabilities.</li><li>
Strong business acumen, including financial and strategic awareness.</li></ul><p></p><p><b>
Why AstraZeneca?</b></p><p>
At AstraZeneca we&rsquo;re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There&rsquo;s no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth, and development. We&rsquo;re on an exciting journey to pioneer the future of healthcare.</p><p><b><br>
So, what&rsquo;s next?
</b></p><ul><li>Are you already imagining yourself joining our team? Good, because we can&rsquo;t wait to hear from you.</li><li>
Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available, and we hope it&rsquo;s yours.</li></ul><p><b>
Where can I find out more?</b></p><p>
Our Social Media, Follow AstraZeneca on LinkedIn</p><p>
Follow AstraZeneca on Facebook</p><p>
Follow AstraZeneca on Instagram</p></div><p></p>

Regulatory Affairs Lead

Thermo Fisher Scientific

<div><p><b>Work Schedule</b></p>
Standard Office Hours (40/wk)<p></p><p><b>
Environmental Conditions</b></p>
Office<p></p><p><b>
Job Description</b></p><p></p><p>
At Thermo Fisher Scientific, you&rsquo;ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our colleagues with the resources needed to achieve career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on &ndash; now and in the future.</p><p></p><p><b>
Location/Division Specific Information</b></p><p>
Our PPD&reg; part of Thermo Fisher Scientific team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic experts. As the world leader in serving science, our Clinical Operations professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations.</p><p></p><h2 class="jobSectionHeader"><b>
Discover Impactful Work:</b></h2><p>
Serves as a senior contact within the Middle East Clinical Operations at CRG, Thermo Fisher Scientific, providing innovative solutions and regulatory expertise. Interacts with clients to offer strategic regulatory intelligence and guidance supporting product development from preclinical stages through registration and product optimization, ensuring compliance with regulatory bodies in the middle east. Provides strategic, expedient, and efficient preparation of client deliverables that meet current local, regional, and ICH regulatory and technical requirements. Acts as a liaison with internal and external clients in the provision and marketing of these specialized regulatory services.</p><p></p><h2 class="jobSectionHeader"><b>
A day in the Life:</b></h2><ul><li>
Prepares and reviews regulatory submissions.</li><li>
Provides regulatory strategy and/or technical advice to internal and external clients, and acts as a liaison in executing strategies.</li><li>
Leads the development and implementation of project-specific processes for sponsors.</li><li>
Collaborates extensively with other departments, regulatory consultants, and regulatory authorities.</li><li>
Assists in identifying and recognizing out of scope activities in a contract in a timely manner and liaises with other departments to follow through on all aspects of contract modifications.</li><li>
Provides training and guidance to junior team members as appropriate.</li><li>
Participates in project launch meetings, review meetings and project team meetings.</li><li>
Supports business development activities, including project budgeting/forecasting</li></ul><p></p><h2 class="jobSectionHeader"><b>
Keys to Success:</b></h2><p></p><p><b>
Mandatory requirements</b></p><ul><li><p>
Saudi Arabia National</p></li><li><p>
Native Arabic speaker</p></li><li><p>
Willingness to be based in Riyadh</p></li></ul><p><b>
Knowledge, Skills, Abilities</b></p><ul><li>
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 3+ years).</li><li>
Bachelor's degree or equivalent and relevant formal academic / vocational qualification</li><li>
Strong English language (written and oral) communication skills as well as local language where applicable</li><li>
Solid understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management; good knowledge of ICH and other global regulatory guidelines; basic understanding of a regulatory speciality areas, such as preclinical, clinical, CMC, publishing, etc.</li><li>
Solid understanding of medical terminology, statistical concepts, and guidelines</li><li>
Capable of working independently and exercising independent judgment to assess sponsor regulatory needs and work with project team members to producing compliant deliverables</li><li>
Solid attention to detail and quality as well as strong editorial/proofreading skills</li><li>
Strong interpersonal skills to work effectively in a team environment and act as a liaison with other departments</li><li>
Solid computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies</li><li>
Solid organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects</li><li>
Solid negotiation skills</li><li>
Strong analytical, investigative and problem-solving skills</li><li>
Working knowledge of budgeting and forecasting&quot;</li></ul><p></p><h2 class="jobSectionHeader"><b>
Work Environment
</b></h2><p></p><p>Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:</p><p></p><ul><li>
Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.</li><li>
Able to work upright and stationary for typical working hours.</li><li>
Ability to use and learn standard office equipment and technology with proficiency.</li><li>
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.</li><li>
May require travel.</li></ul><p></p><h2 class="jobSectionHeader"><b>
Benefits</b></h2><p></p><p>
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!</p></div><p></p>

Senior Regulatory Affairs Specialist - GCL

<div><p>WSP in the Middle East are seeking a dynamic and experienced Senior Government Relations Manager_Saudi National, to join our growing team in Riyadh, KSA.
<br>
This role offers an exciting opportunity for a motivated Saudi national to lead key government relations functions while working in a collaborative, high-performance environment.</p></div>
<br><div><ul><li>Team Leadership: Independently manage relationships with senior stakeholders while guiding and supporting junior team members across related functions.
</li><li>Company Licenses &amp; Registration: Manage and maintain all company licenses and registrations with local authorities, ensuring timely renewals and full compliance.
</li><li>Visa &amp; Iqama Management: Oversee all employee visa and Iqama processes, including onboarding, renewals, and extensions.
</li><li>Qiwa Employment Contracts: Administer employment contracts via the Qiwa system, ensuring alignment with current labor laws and regulations.
</li><li>Regulatory Compliance: Monitor and ensure full adherence to Saudi labor laws and evolving government regulations.
</li><li>Policy Development: Develop and update internal policies and procedures related to employee management, visa processing, and regulatory compliance.
</li><li>Stakeholder Management: Serve as the primary liaison between WSP and government authorities, managing official communications, approvals, and inquiries.
</li><li>Government Engagement: Build and maintain strong relationships with key government entities to support the company&rsquo;s regulatory positioning and public reputation.
</li><li>Employee Database Management: Maintain and update the organization&rsquo;s employee database, ensuring data accuracy and integrity for all government relations (GR) processes.
</li><li>Reporting &amp; Documentation: Produce and submit regular reports on all GR-related activities and ensure timely delivery of any ad hoc reports requested by management. Provide accurate documentation, reporting, and data management with advanced proficiency in Microsoft Excel.
</li><li>Industry Awareness: Stay up to date with the latest government relations trends, platform updates (e.g., Qiwa, GOSI, Muqeem), and best practices to continuously improve internal processes.
</li><li>Labor Dispute Resolution: Support the resolution of labor-related cases in compliance with Saudi labor law and company policy.</li></ul></div>
<br><div><ul><li>Saudi National with a Bachelor's degree in a relevant field.
</li><li>Minimum of 8 years&rsquo; experience in government relations, public affairs, or a similar role&mdash;preferably within the engineering, construction, or consulting sectors.
</li><li>Strong track record of independently managing internal and external stakeholders, including cross-functional teams and government bodies.
</li><li>The ability to perform under pressure and meet deadlines in a fast-moving, high-demand environment.
</li><li>Deep understanding of Saudi governmental systems, labor laws, and regulatory frameworks.
</li><li>Strong communication, negotiation, and interpersonal skills. Advanced Microsoft Excel skills for efficient data and process management.
</li><li>High level of professionalism and discretion in handling legal and regulatory matters.
</li></ul><p><b>Imagine a better future for you and a better future for us all.
</b></p><p>Join our close-knit community of talented individuals who share your passion for making a positive impact. Our global team includes more than 69,000 employees, working together to make a difference in communities both close to home and around the world.
</p><p><b>With us, you can. Apply today.</b></p></div><br><div></div>

Government Relations Manager _Saudi National

Analytix Arabia Management Consultant pvt ltd

<p><b>Position Overview:</b><br/>Lead and manage end-to-end factory setup projects and associated licensing activities in Saudi Arabia, ensuring full regulatory compliance and alignment with Vision 2030. Serve as the primary liaison between government entities, clients, and internal teams to secure all necessary approvals efficiently and on time.</p><p><b>Key Responsibilities:</b></p><ul><li>Lead the full lifecycle of factory establishment and licensing projects across the Kingdom.</li><li>Build and maintain high-level relationships with key government authorities and regulatory bodies.</li><li>Ensure all projects comply with Saudi Arabia&rsquo;s industrial, labor, and regulatory requirements.</li><li>Coordinate and guide internal teams, external consultants, and stakeholders to ensure accurate and timely submissions.</li><li>Provide strategic advice to senior management and represent Analytix in official meetings and public forums.</li></ul><p><b>Qualifications:</b></p><ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in Business, Engineering, or a related field.</li><li>Minimum 10 years of senior-level experience in project management or licensing within Saudi Arabia.</li><li>Proven track record in navigating government relations and regulatory frameworks.</li><li>Strong leadership, negotiation, and communication skills.</li><li>Fluency in English is required; Arabic proficiency is highly preferred.</li></ul><p>Job Types: Full-time, Permanent</p>

Project Manager

Bechtel

<div><p><b>Requisition ID: </b><b>287645</b></p><ul><li><b>
Relocation Authorized: </b><b>None</b></li><li><b>
Telework Type: </b><b>Full-Time Office/Project</b></li><li><b>
Work Location: Riyadh</b></li></ul><p><br>
</p><div><div><div><h2 class="jobSectionHeader"><b>Extraordinary teams building inspiring projects:</b></h2></div><div><p>
Since 1898, we have helped customers complete more than 25,000 projects in 160 countries on all seven continents that have created jobs, grown economies, improved the resiliency of the world's infrastructure, increased access to energy, resources, and vital services, and made the world a safer, cleaner place.</p><p>
Differentiated by the quality of our people and our relentless drive to deliver the most successful outcomes, we align our capabilities to our customers' objectives to create a lasting positive impact. We serve the Infrastructure; Nuclear, Security &amp; Environmental; Energy; Mining &amp; Metals, and the Manufacturing and Technology markets. Our services span from initial planning and investment, through start-up and operations.</p><p>
Core to Bechtel is our Vision, Values and Commitments. They are what we believe, what customers can expect, and how we deliver. Learn more about our extraordinary teams building inspiring projects in our Impact Report.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Project Overview:</b></h2></div><div><div>
Bechtel Mining and Metals offers engineering, procurement, and construction services for customers in the mining sector across multiple commodities including Iron Ore, Bauxite, Alumina, Aluminium, Copper, Gold, Coal, Lithium and Rare Earths markets.</div><div>
</div><div>
Headquartered in Santiago, Chile, the M&amp;M global business unit also has offices in Brisbane, Perth and Adelaide in Australia along with execution units in the United States, Peru, Kingdom of Saudi Arabia, India and other project locations around the world.</div></div></div><div><div><h2 class="jobSectionHeader"><b>
Job Summary:</b></h2></div><div><p>
In this role, you will work directly with the customer Permitting manager to identify all Permit requirements to support successful project execution and coordinate stakeholder engagement with project personnel, regulatory and government agencies to facilitate required approvals</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Major Responsibilities:</b></h2></div><div><ul><li>
Plans, implements, and maintains the project permitting and stakeholder engagement registers to track deliverables against project schedule.</li><li>
Serves as a technical expert for the project, on permitting requirements and stakeholder engagement strategies.</li><li>
Monitors and facilitates progress of permitting deliverables consistent with strategies, goals, measurements, and reporting standards</li><li>
Coordinates with and provides technical assistance to other project functional leads (e.g., procurement, construction, planners, project controls) with regards to developing project-specific permitting requirements to ensure any commitments are integrated fully and appropriately.</li><li>
Anticipates and manages issues, with particular emphasis on issues that have, or have the potential to, impact the constructability of the project and/or project reputation.</li><li>
Provides strategic advice for the project to manage the implementation of permitting and stakeholder requirements ensuring alignment with the project social and environmental performance commitments and strategy.</li><li>
Provides strategic advice to project teams on potential impacts, expectations, and related implications; assesses consequences of project decisions; and works with project functional teams to develop proactive solutions to community and environmental issues to minimize external risks and manage public expectations.</li><li>
Leads community engagement and consultation in partnership with the customer.</li><li>
Supports ongoing understanding of national and regional priorities and plans and keeps abreast of legislative developments, stakeholder interests and concerns, and other influential trends.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Education and Experience Requirements:</b></h2></div><div><ul><li>
Bachelor's degree (or international equivalent) and 10-13 years of relevant experience or 14-17 years of relevant work experience</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Required Knowledge and Skills:</b></h2></div><div><ul><li>
The successful candidate will have established relationships with key regulatory and agency stakeholders and relevant experience in securing major project permits in Kingdom. Being fluent in Arabic and English language is also a key requirement for the role.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Total Rewards/Benefits:</b></h2></div><div><p>
For decades, Bechtel has worked to inspire the next generation of employees and beyond! Because our teams face some of the world's toughest challenges, we offer robust benefits to ensure our people thrive. Whether it is advancing careers, delivering programs to enhance our culture, or providing time to recharge, Bechtel has the benefits to build a legacy of sustainable growth. Learn more at Bechtel Total Rewards</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Diverse teams build the extraordinary:</b></h2></div><div><p>
As a global company, Bechtel has long been home to a vibrant multitude of nationalities, cultures, ethnicities, and life experiences. This diversity has made us a more trusted partner, more effective problem solvers and innovators, and a more attractive destination for leading talent.</p><p>
We are committed to being a company where every colleague feels that they belong-where colleagues feel part of &quot;One Team,&quot; respected and rewarded for what they bring, supported in pursuing their goals, invested in our values and purpose, and treated equitably.</p></div></div></div><p></p><p><b><i><br>
Bechtel is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity and expression, age, national origin, disability, citizenship status (except as authorized by law), protected veteran status, genetic information, and any other characteristic protected by federal, state or local law. Applicants with a disability, who require a reasonable accommodation for any part of the application or hiring process, may e-mail their request to </i></b><b>acesstmt@bechtel.com</b></p></div>

Permitting/Stakeholder Manager

Explore 972+ Regulatory affairs manager in Riyadh this October. Find roles across top companies and apply now to boost your career.