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regulatory affairs specialist

<div>Site Name: Riyadh Olaya Towers 
Posted Date: Jul 31 2025 
GSK Saudi Arabia is committed to supporting Vision 2030 and the Saudi Arabian National Agenda including Saudization in line with the hiring and the training and development of Saudi National capability.
Are you energized by a highly impactful regulatory affairs role that allows you to shape and accelerate regulatory effectiveness across the organization? If so, this Regulatory Affairs Specialist role could be an ideal opportunity to explore.
As Regulatory Affairs Specialist, you will be responsible for leading or supporting strategic and operational Regulatory projects, which support business strategy and platform delivery.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following&hellip;<ul><li>
Fulfil standard, ad hoc, or complex data reporting request and design outputs.</li><li>
Assist Regulatory Business Operations (RBO) staff in delivery of projects.</li><li>
Assist RBO staff in process documentation, monitoring, and reporting.</li><li>
Maintain Team sites.</li><li>
Adhere to records retention.</li><li>
Complete appropriate training.</li><li>
Assist Regulatory Business Operations staff to optimize project plan robustness (scope, deliverables, resources, timing).</li><li>
Provide project support to meet assigned business deliverables.</li><li>
Edit existing process documentation and lead monitoring and reporting.</li><li>
Provide analysis and interpretation of information in response to requests from requestors and pursue greater data quality through identification of gaps and delivery of efficient solutions.</li></ul>
Why you?
Basic Qualifications:
We are looking for professionals with these required skills to achieve our goals:<ul><li>
Saudi national.</li><li>
Bachelor&rsquo;s degree.</li><li>
3 years of pharmaceutical industry experience in a regulatory environment.</li><li>
Experience with License Maintenance as well as overall R&amp;D processes.</li><li>
Direct experience with project planning &amp; execution.</li></ul>
Preferred Qualifications:
If you have the following characteristics, it would be a plus:<ul><li>
Master&rsquo;s degree or MBA</li><li>
Experience working in a matrixed environment</li><li>
Demonstrated ability to engage and influence senior stakeholders.</li></ul>
Closing Date: 08 August 2025
Why GSK?
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose &ndash; to unite science, technology and talent to get ahead of disease together &ndash; so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns &ndash; as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it&rsquo;s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves &ndash; feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.
Contact information:
You may apply for this position online by selecting the Apply now button.
Important notice to Employment businesses/ Agencies
GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</div> <div id='job-id'>Job Id: 7b5+jGP9Lc5Dn3GrxTo/Tl1+RPMq8PHNrAALL2vRxxNdl3wgFH2NblNsIXfoyVZ1OAvnr/LN5VL+Yb4gIkOt4mUsf2wq5S3IOwPVch/r8C++lwWM1g==</div>

Regulatory Affairs Specialist

Novartis

<div><div><h3 class="jobSectionHeader">Summary
</h3><div>Be the bridge between innovation and patient safety&mdash;As a Regulatory Affairs Specialist in Saudi Arabia&rsquo;s dynamic healthcare landscape, you&rsquo;ll play a pivotal role in shaping the future of medicine. From ensuring compliance with SFDA regulations to accelerating access to life-saving therapies, your expertise drives both public health and industry growth. Join a mission where precision meets purpose, and every regulation you navigate brings better care to millions.</div>
</div><div><h3 class="jobSectionHeader">About the Role
</h3><div>Major Accountabilities
<ul><li>New Product Registrations &ndash; With supervision, evaluate, and prepare drug registration applications in a timely manner and follow through the application during the evaluation phase to achieve a favorable outcome</li><li>
Maintenance of registered products &ndash; With supervision, maintain registration of currently approved products (initiation and preparation of variation/ and renewal applications as per the plan communicated from the DRA manager/Head).</li><li>
Coordinate with DRA manager/head to ensure correct and speedy implementation / consignments as per the approved applications (variation/ renewal/ site transfer/ site registration/leaflet update).</li><li>
Maintain, with supervision, the internal DRA database accurate and updated: Dragon/DASA</li><li>
Relationships within and outside the company - Develop and maintain good working relationships with other Novartis departments both locally and with Head Office and with third-party vendors.</li><li>
With Supervision, Review PPMS and ensure AQWA Launch request are prepared and launched on time.</li><li>
With Supervision, ensure full support to Global regulatory compliance initiatives in Saudi.</li></ul>
Minimum Requirements<ul><li>
Pharmacy or related science degree.</li><li>
Minimum 1 year of RA Experience in reputable pharmaceutical company.</li><li>
Experience handling a portfolio/product and dealing with stakeholder such as SFDA and governmental agency.</li><li>
Must be Saudi national.</li></ul> 
#LI-Onsite</div>
</div><div><div>Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
Benefits and Rewards: Read our handbook to learn about all the ways we&rsquo;ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards</div></div></div>
 <div><div>Division
<div>Development
</div></div><div>Business Unit
<div>Innovative Medicines
</div></div><div>Location
<div>Saudi Arabia
</div></div><div>Site
<div>Riyadh
</div></div><div>Company / Legal Entity
<div>SAP0 (FCRS = CH024) Novartis Consulting AG
</div></div><div>Functional Area
<div>Research &amp; Development
</div></div><div>Job Type
<div>Full time
</div></div><div>Employment Type
<div>Regular
</div></div><div>Shift Work
<div>No</div></div><div> 
</div><div>Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.</div></div><div></div> <div id='job-id'>Job Id: eTktN/ajFZ95Bj/U3ZZyNF16WqJNxVr7wxN8Cg9UsxZE35y3UqwOsMxrHFaB0VRQOzmwPyMJqD4h1dChEXFgDT95w2WIznm4VMrLExe59oq205/9mfqYVKfpB1BMk7/eSjW8UInil5Cq57Wm+AxE79zV2XQhCCiN+ksSsVUnbnax</div>

Cardinal Health

<div><div>Specialist, Quality &amp; Regulatory Affairs
At Cardinal Health, we aim to be a trusted partner, offering a broad range of innovative solutions that help our customers provide cost-efficient, more effective healthcare. Join our team of 50,000 humble partners striving each day to make healthcare more efficient, providers more effective, and patients as healthy as possible.
We are currently looking to recruit a Specialist Quality &amp; Regulatory Affairs based in our Riyadh office in Saudi Arabia, reporting to the Quality and Regulatory Affairs Manager, you will be responsible for, but not limited to, the following:<ul><li>
Ensuring accurate and timely registration of products with competent authorities for KSA and other EMEA markets.</li><li>
Provide Quality &amp; Regulatory Affairs support for EMEA markets, in compliance with applicable regulations and standards to ensure timely commercialization of products.</li><li>
Develop and execute registration strategy in close partnership with Global RA &amp; local RA manager.</li><li>
Support regional distribution control (in compliance with applicable regulations and standards) to ensure timely commercialization of products.</li><li>
Review and validate regulatory data executing outbound flow.</li><li>
Ensure deployment and improvement of regulatory document related to new project development.</li><li>
Support as required the EMEA QRA team to ensure quality and regulatory compliance in accordance with national and European regulations.</li><li>
Act as the QRA representative in regional project meeting.</li></ul>
Essential Functions and Responsibilities
With moderate supervision, you will be responsible for the following Regulatory and Quality activities:<ul><li>
Developing and implementing regulatory strategies and processes to ensure timely commercialization of products in compliance with applicable regulations and standards.</li><li>
Preparing documentation to support product registration and modifications according to project phase implementation.</li><li>
Overall registration strategies, coordination, implementation, execution, control and completion of product registrations in EMEA countries.</li><li>
Providing Regulatory intelligence.</li><li>
Supporting communication with our local agent and distributors in EMEA countries.</li><li>
Acting as QRA representative in the project implementation and work activity with various stakeholders.</li><li>
Notification to the regional quality and regulatory team for sharing status&rsquo; &amp; updates of ongoing projects.</li><li>
Monitoring of local Regulatory environment, new regulations and supporting feedback and gap assessments to international Regulatory departments and business partners that impact projects.</li></ul></div><div><ul><li>
Ensuring follow-up/improvement of the distribution control procedure.</li><li>
Maintaining and archiving of all regulatory documentation in the region.</li><li>
Where needed, supporting the reporting of Serious Adverse Events to Competent Authority(ies) in EMEA.</li><li>
Ensuring compliance with quality procedures, laws and regulations of the applicable markets.</li><li>
Communicating business related issues or opportunities to next management level.</li><li>
Ensuring personal and company compliance with all local and company regulations, policies, and procedures.</li><li>
Training and deployment of local tools related to distribution control.</li><li>
Ensuring QRA administrative tasks related to assigned projects are completed.</li><li>
Perform other duties assigned as needed.</li></ul>
Qualifications and Experience<ul><li>
BA/BS in Scientific discipline or equivalent work experience (3 years min).</li><li>
BS degree in Pharmacy, Medicine, Physical or Biological science or similar obtained by experience.</li><li>
Minimum of 3 years&rsquo; experience in Regulatory Affairs in Saudi Arabia and MEA region.</li><li>
Fluency in written and verbal English and Arabic is mandatory.</li><li>
Consistent background and knowledge of SFDA regulations for Medical Devices, strong connections with SFDA will be preferred.</li><li>
Must be proficient with MS Office applications.</li><li>
Excellent communication skills (verbal and written).</li><li>
Project management skills preferred.</li><li>
Problem solving skills.</li><li>
Presentation skills preferred.</li><li>
High degree of initiative.</li><li>
Open minded, listens to others.</li><li>
Able to manage complexity within a matrix organization.</li><li>
At ease in international environment.</li><li>
Hands on/can do attitude.</li><li>
Excellent attention to details.</li></ul>
Benefits<ul><li>
Comprehensive local medical insurance for the employee and his/her family</li><li>
Various allowances</li><li>
Long term disability support, etc.</li></ul></div>
The Company
Headquartered in Dublin, Ohio, Cardinal Health (NYSE: CAH) is a health care services company that improves the cost-effectiveness of healthcare. As the business behind healthcare, Cardinal Health helps pharmacies, hospitals and ambulatory care sites focus on patient care while reducing costs, improving efficiency and quality, and increasing profitability. Cardinal Health is an essential link in the healthcare supply chain, providing pharmaceuticals and medical products to more than 100,000 locations each day and is also the industry-leading direct-to-home medical supplies distributor. The company is a leading manufacturer of medical and surgical products, including gloves, surgical apparel and fluid management products. In addition, the company supports the growing diagnostic industry by supplying medical products to clinical laboratories and operating the nation's largest network of radio pharmacies that dispense products to aid in the early diagnosis and treatment of disease. Ranked #14 on the Fortune 500, Cardinal Health employs more than 50,000 people worldwide.
Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply.
Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.</div> <div id='job-id'>Job Id: DceBc40TX790c/o/yjPb/15Hhem7v4r+EVdsVMLg5wsj1z3yWzijSd0OtxXxRNhOWQhkEyd+FzvekWzrjboKuQAIxPQzIqd0JNev8Un36/sdeuMc87WuRyTr3bnBu0wCifuX3sWj/o+RBRgwF0wrSIoS5dkY5GCimeZhzw4DROEzvJtB7BaM9s3qzquJp5rIelbsRGONc1cXDHXm8LZgOSSzD8Z+mykWrwj4IHj2+Hgc2vbq4rV9MylScnE5f394TY5x/GsrMzPIjQqLZjYCa6D/dNXlYzVOwBMcMNmnkoyGbJNg</div>

Specialist, Quality & Regulatory Affairs

Roche

<div>At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.<div>
The Position</div>
The Opportunity
The Regulatory Affairs Business Lead is responsible for developing and executing submission and approval strategies for all regulatory activities, ensuring ethical conduct and compliance with laws and regulations.
Your Responsibilities<ul><li>
Manage, supervise and coach Regulatory Affairs associates to achieve the business objectives in terms of new Launches and life cycle maintenance activities.</li><li>
Work with Affiliate DRA Head (Operations Director) to identify and recommend appropriate Regulatory Affairs resources and budget.</li><li>
New product registration, set up the strategy, evaluate, prepare and submit drug registration application in a timely manner and follow through the application during the evaluation phase to achieve a favorable outcome.</li><li>
Direct engagement with local authorities in building business initiatives.</li><li>
Provide Regulatory Affairs input into relevant cross-functional Affiliate business strategies (e.g. market access, medical affairs, promotional activities, public policy, technical assessments, technical agreements, local manufacturing/packaging activities, legal issues, etc.).</li><li>
Develop innovative, risk-based regulatory strategies and work plans for assigned products or business areas within the Affiliate to accelerate access in alignment with global.</li><li>
Ensure the compliance of the Regulatory database system&rsquo;s content &amp; data maintenance activities.</li><li>
Support regulatory inspection-readiness for the Affiliate, including leading or participating in internal/external regulatory audits (by ensuring the proper achieving, system accurate and timely manner entries).</li><li>
Interact and negotiate with local HAs, external and internal stakeholders (meetings, calls, emails, and visits).</li></ul>
Who You Are<ul><li>
Bachelor&rsquo;s degree in Pharmacy Sciences.</li><li>
7+ years of experience preferably has worked in the field.</li><li>
Efficient team management and leadership.</li><li>
Fluency in communication in both languages (English &amp; Arabic).</li><li>
Proficiency in SAP system.</li></ul><div>
Who we are</div>
A healthier future drives us to innovate. Together, more than 100&rsquo;000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. 
Let&rsquo;s build a healthier future, together.
Roche is an Equal Opportunity Employer.</div> <div id='job-id'>Job Id: jKlbYzr4vLkg2S1xyQbhrBVGdVJrd6WyKM5qAGKRhdDjk1SpsmMv1xVb8+kvyFDrEuMCImTdT2KstA9ZiPxK8ktKnKq8Oo0JFkafXbrOM+k8</div>

Regulatory Affairs Business Lead

<div>
 At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
 
 
 The Position
 
 
 
 The Opportunity
 
 
 
 The Regulatory Affairs Business Lead is responsible for developing and executing submission and approval strategies for all regulatory activities, ensuring ethical conduct and compliance with laws and regulations.
 
 
 
 Your Responsibilities
 
 
 <ul>
 <li>
 Manage, supervise and coach Regulatory Affairs associates to achieve the business objectives in terms of new Launches and life cycle maintenance activities
 </li>
 <li>
 Work with Affiliate DRA Head (Operations Director) to identify and recommend appropriate Regulatory Affairs resources and budget
 </li>
 <li>
 New product registration, set up the strategy, evaluate, prepare and submit drug registration application in a timely manner and follow through the application during the evaluation phase to achieve a favorable outcome
 </li>
 <li>
 Direct engagement with local authorities in building business initiatives
 </li>
 <li>
 Provide Regulatory Affairs input into relevant cross-functional Affiliate business strategies (e.g. market access, medical affairs, promotional activities, public policy, technical assessments, technical agreements, local manufacturing/packaging activities, legal issues, etc.)
 </li>
 <li>
 Develop innovative, risk-based regulatory strategies and work plans for assigned products or business areas within the Affiliate to accelerate access in alignment with global
 </li>
 <li>
 Ensure the compliance of the Regulatory database system&rsquo;s content &amp; data maintenance activities
 </li>
 <li>
 Support regulatory inspection-readiness for the Affiliate, including leading or participating in internal/external regulatory audits (by ensuring the proper achieving, system accurate and timely manner entries)
 </li>
 <li>
 Interact and negotiate with local HAs, external and internal stakeholders (meetings, calls, emails, and visits)
 
 
 
 </li>
 </ul>
 
 Who You Are
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Pharmacy Sciences
 </li>
 <li>
 7+ years of experience preferably has worked in the field.
 </li>
 <li>
 Efficient team management and leadership
 </li>
 <li>
 Fluency in communication in both languages (English &amp; Arabic).
 </li>
 <li>
 Proficiency in SAP system
 
 
 </li>
 </ul>
 Who we are
 
 
 A healthier future drives us to innovate. Together, more than 100&rsquo;000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
 
 
 Let&rsquo;s build a healthier future, together.
 
 
 
 Roche is an Equal Opportunity Employer.
 
</div>
 <div id='job-id'>Job Id: 2E1OQS9oL5WvSX+EbbqHZqk7Vybm7c8tJh576kMETnzpUF5fGWDx1aPYCijGqKzx09KIaB7SZEYir63oEscj0hnC11ouT1DYyYoxvPnvz78sK03NvGMJr+kS4nqwCWLO74vVAEVocsiD7N+coOI5BAz12s6hf2F/5RwdrlD8lNlIqqNjlswU2H+w9MloEGKq1NjhI0pOfhdqvYzxdJzDiIQOQ19KpI6sixeCe5+h4w/kzcD7g/Hk</div>

Parsons

<div>In a world of possibilities, pursue one with endless opportunities. Imagine Next!
When it comes to what you want in your career, if you can imagine it, you can do it at Parsons. Imagine a career working with intelligent, diverse people sharing a common quest. Imagine a workplace where you can be yourself. Where you can thrive. Where you can find your next, right now. We&rsquo;ve got what you&rsquo;re looking for.
Job Description:
Parsons is looking for an amazingly talented Senior Reporting Specialist (Saudi National) to join our team!
What You&rsquo;ll Be Doing:
Project Reporting &amp; Data Management:
<ul><li>Lead the preparation and consolidation of daily, weekly, and monthly reports across multiple workstreams including engineering, construction, HSE, quality, and commercial.
</li><li>Manage and validate project performance data, ensuring accuracy and consistency across dashboards, KPIs, and progress trackers.
</li><li>Coordinate the integration of reporting inputs from consultants, contractors, and subcontractors.
</li></ul>Performance Analytics &amp; Dashboards:
<ul><li>Develop and maintain visual performance dashboards and analytical tools to support senior management and client briefings.
</li><li>Analyze trends and highlight variances in schedule, cost, and resource metrics using industry-standard reporting methodologies (e.g., Earned Value Management).
</li><li>Provide advanced insights on project performance risks and recommend mitigation strategies.
</li></ul>Stakeholder Coordination &amp; Communication:
<ul><li>Interface regularly with planning, cost, engineering, and construction teams to align reporting outputs with project progress.
</li><li>Collaborate with client representatives and external stakeholders to ensure compliance with contractual and regulatory reporting requirements.
</li><li>Represent the reporting function in progress meetings, coordination reviews, and executive briefings.
</li></ul>Standardization &amp; Quality Control:
<ul><li>Ensure all reports meet established quality standards, templates, and branding guidelines.
</li><li>Lead the continuous improvement of reporting systems and procedures for enhanced efficiency and clarity.
</li><li>Train and mentor junior reporting staff in data handling, report writing, and visualization techniques.
</li></ul>What Required Skills You&rsquo;ll Bring:
Education:
<ul><li>Bachelor&rsquo;s degree in Engineering, Project Management, Data Analytics, or a related field.
</li></ul>Experience:
<ul><li>Minimum 8 years of experience in project reporting and analytics, preferably within large infrastructure or airport/airfield projects .
</li><li>Proven ability to manage complex datasets and reporting workflows in multi-stakeholder project environments.
</li></ul>Skills &amp; Knowledge:
<ul><li>Advanced proficiency in Microsoft Excel, Power BI, and PowerPoint; working knowledge of Primavera P6 , Aconex, or MS Project is preferred.
</li><li>Strong understanding of project controls principles including planning, scheduling, budgeting, and progress measurement.
</li><li>Excellent writing and presentation skills, with the ability to distill technical content into clear executive summaries.
</li><li>Detail-oriented with strong organizational skills and the ability to manage competing deadlines.
</li></ul>What Desired Skills You&rsquo;ll Bring:
<ul><li>Certification in Project Controls, PMP, or Data Analytics is an asset.
</li><li>Familiarity with Earned Value Management (EVM), S-curve generation, and productivity tracking tools.
</li><li>Experience working on airfield construction or aviation infrastructure projects.
</li><li>Knowledge of report automation tools and database integration is a plus.
</li><li>Fluency in English (written and spoken); Arabic is an advantage.
</li></ul>Parsons equally employs representation at all job levels no matter the race, color, religion, sex (including pregnancy), national origin, age, disability or genetic information.
We truly invest and care about our employee&rsquo;s wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest&mdash;APPLY TODAY!
Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to https://www.parsons.com/fraudulent-recruitment/ .</div> <div id='job-id'>Job Id: +duwnivbtfDu/aeKPOzv8GFBC77RY8rBAEJ3xACglUV6PfE8G2oOKDNkTQr1aR1I++mgOliubcr1wpVQpLPLV7CCi+XzGqSu9b+VSCBEkct6asl8LBqxZV5H4g0SBEaXfmiRfAb0XmzyTsyvpiJc27C3D4HlopT73jdfdQILia8nVodnYFgv9Q+wUZb8Bhha5cTQv5I=</div>

Senior Reporting Specialist (Saudi National)

Basharsoft

<div>Job Title: Government Relations Officer 
Location: Riyadh, Saudi Arabia
A holding company operating across multiple sectors in Saudi Arabia is seeking a Government Relations Officer to manage and facilitate all governmental interactions, documentation, and compliance processes.
The ideal candidate will act as the main liaison between the company and various government bodies to ensure seamless operations, legal adherence, and timely approvals for company initiatives, employees, and corporate assets<h3 class="jobSectionHeader">
Duties and Responsibilities</h3><ul><li>
Handle all government-related transactions and services, including visas, Iqama processing, renewals, labor office visits, GOSI, chamber of commerce, and municipality interactions.</li><li>
Maintain strong relationships with key government agencies such as the Ministry of Labor, Ministry of Investment (MISA), GOSI, ZATCA, Ministry of Interior, Civil Defense, and others.</li><li>
Ensure timely compliance with Saudi labor laws, Saudization policies, and other regulatory requirements.</li><li>
Track and manage all legal and governmental documents and licenses, including renewal dates, submissions, and regulatory filings.</li><li>
Assist in the onboarding process for expatriates by facilitating work/residency permits, license registrations, and relocation procedures.</li><li>
Monitor changes in local legislation and update internal stakeholders with potential business impacts.</li><li>
Coordinate with legal and HR departments to resolve compliance-related matters.</li><li>
Represent the company in meetings, inspections, and other official engagements with government authorities.</li><li>
Maintain a digital and physical record of all official documents and approvals.</li></ul><h3 class="jobSectionHeader">
Qualifications and Requirements</h3><ul><li>
Saudi National (mandatory).</li><li>
Bachelor&rsquo;s degree in Business Administration, Law, or a related field.</li><li>
Minimum 3&ndash;5 years of experience in government relations within a corporate setting in Saudi Arabia.</li><li>
Strong knowledge of Saudi labor law, visa and work permit procedures, and government portals (e.g., Muqeem, GOSI, Qiwa, Balady, Absher).</li><li>
Excellent communication and negotiation skills in both Arabic and English.</li><li>
High level of professionalism, confidentiality, and integrity.</li><li>
Proficient in Microsoft Office and document management systems.</li><li>
Valid Saudi driver&rsquo;s license and willingness to travel locally for government visits.</li></ul></div> <div id='job-id'>Job Id: pz/zkRlPP7nA1jUXIqyFTzRU8C1MKt4LXS8zH02rTocWi+mL9KjpkT44rrNfL/Esjni/+tO64mmRMucYYfboK5yf2HuNAXLZ7kVIaW2vkIASnDBAUbcDk4rZD2yd</div>

Government Relations Officer

Explore 450+ Regulatory affairs specialist in Riyadh this August. Find roles across top companies and apply now to boost your career.

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