procurement specialist

legal specialist

senior commercial manager

sales specialist

senior project manager

senior regulatory affairs specialist

Thermo Fisher Scientific

<div>Work Schedule
Standard Office Hours (40/wk)
Environmental Conditions
Office
Job Description
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.
Location/Division Specific Information
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.<h2 class="jobSectionHeader">
Discover Impactful Work:</h2>
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.<h2 class="jobSectionHeader">
A day in the Life:</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><h2 class="jobSectionHeader">
Keys to Success:</h2>
Mandatory requirements<ul><li>
Saudi Arabia National</li><li>
Native Arabic speaker</li><li>
Willingness to be based in Riyadh</li></ul>
Knowledge, Skills, Abilities<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><h2 class="jobSectionHeader">
Work Environment
</h2>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:<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><h2 class="jobSectionHeader">
Benefits</h2>
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!</div>

Senior Regulatory Affairs Specialist - GCL

Johnson & Johnson

<div>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
Job Function:
Regulatory Affairs Group
Job Sub Function:
Regulatory Product Submissions and Registration
Job Category:
Professional
All Job Posting Locations:
Riyadh, Saudi Arabia
Job Description:
About MedTech
Fueled by innovation at the intersection of biology and technology, we&rsquo;re developing the next generation of smarter, less invasive, more personalized treatments.
Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech
REGULATORY AFFAIRS SPECIALIST (MEDICAL DEVICES)
Location: Riyadh
Contract: full-time
Purpose:
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.
You will be responsible for:<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>
Qualifications / Requirements:<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>JOB TITLE
Regulatory Affairs Lead 
ABOUT ASTRAZENECA
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.
ROLE SUMMARY
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.
What you&rsquo;ll do
Regulatory Strategy &amp; Submissions<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>
Business Partnering &amp; Country RA Agenda<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>
Leadership &amp; People Development<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>
External Engagement &amp; Business Awareness<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>
Governance &amp; Compliance<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>
Only applications in KSA will be considered.
Essential for the role<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>
Why AstraZeneca?
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. 
So, what&rsquo;s next?
<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>
Where can I find out more?
Our Social Media, Follow AstraZeneca on LinkedIn
Follow AstraZeneca on Facebook
Follow AstraZeneca on Instagram</div>

Regulatory Affairs Lead

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 Permitting Office Senior Coordinator to join our team! In this role you will get to perform key tasks within a fast-paced team to meet permitting and other requirements within complex workflows involving multiple parties.
What You'll Be Doing:
<ul><li>Update basic tracking solutions (using tools like Excel, PowerPoint, M365, Planner) for active work within the Permitting Office and across the Business Units
</li><li>Track and record printed letters, wet-signatures, and distribution of final/copies/scans of signed letters
</li><li>Oversee the contents and access management of the Permitting Office Sharepoint site
</li><li>Provide coordination and logistics support for meetings, reports and other Permitting Office needs
</li><li>Support the Director, Senior Managers and other team members to stabilize the external engagement and internal workflows by providing Senior Coordinator skills and effort
</li></ul>What Required Skills You'll Bring:
<ul><li>High school diploma (or equivalent) and typically 4+ years of relevant work experience, including 3+ years of prior document control experience.
</li><li>Proficiency in MS Office with expertise in Microsoft Word, PowerPoint, Excel, Sharepoint and document management systems.
</li><li>Good written and oral communication, organizational, and interpersonal skills, as well as a demonstrated ability to interact effectively with project personnel and management.
</li><li>English and Arabic fluency.
</li></ul>What Desired Skills You'll Bring:
<ul><li>Experience working with government-related, regulatory and/or legal documents
</li><li>Experience working in Riyadh, KSA with large programs and national / local government organizations
</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>

Senior Coordinator - Permitting Office (Saudi National)

Emdad By Elm

<div>
 
 
 Job Description:
 
 
 
 To develop and draft organizational policies and related studies, ensuring alignment with applicable regulations and directives. The role includes updating internal policies based on supervisory circulars to maintain compliance and enhance institutional governance.
 
 
 
 
 
 
 Key Responsibilities:
 
 
 <ul>
 <li>
 Draft and develop internal policies in line with best practices and approved standards
 </li>
 <li>
 Conduct pre-legislative studies to assess regulatory and operational impact
 </li>
 <li>
 Review and update policies in response to circulars and directives from supervisory authorities
 </li>
 <li>
 Coordinate with relevant departments to ensure policy alignment with internal procedures
 </li>
 <li>
 Prepare policy reports and submit recommendations to senior management
 </li>
 <li>
 Monitor regulatory changes and analyze their implications on existing policies
 </li>
 <li>
 Contribute to building a structured policy knowledge base and documentation system
 </li>
 </ul>
 
 
 
 
 
 Qualifications:
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Business Administration, Law, or a related field
 </li>
 <li>
 Minimum of 3 years&rsquo; experience in policy development, governance, or regulatory affairs
 </li>
 <li>
 Solid understanding of local regulations and supervisory circulars
 </li>
 <li>
 Strong analytical and writing skills
 </li>
 <li>
 Proficiency in Microsoft Office; familiarity with policy management systems is a plus
 </li>
 </ul>
 
 
</div>

Policy Specialist

Amazon Web Services (AWS)

<div>
 
 Description
 
 
 
 Would you like to be part of a public policy team focused on increasing awareness and adoption of Amazon Web Services (AWS)* services cloud amongst enterprises, public sector and regulated industries (e.g., financial services and healthcare) in the Kingdom of Saudi Arabia? Do you have government affairs experience and have the technology public policy experience necessary to help further advance Amazon as a leading cloud platform provider in the Kingdom?
 
 
 Amazon Web Services is the leading provider of cloud computing services, providing IT infrastructure offerings such as on-demand compute capacity, storage, content delivery, database services and more. We are looking for a talented, innovative individual to represent AWS in the Kingdom of Saudi Arabia before policymakers. The successful candidate will proactively build relationships with key policymakers, IT decision makers and executives in government and other relevant organizations and help prioritize international, national, and regional government public policy issues faced by AWS customers. You will address policy risks to AWS customers as well as advance strategic business opportunities and initiatives in the IT services industry. This position will also support AWS&rsquo;s participation in key business associations that are critical to advancing AWS public policy and business objectives. You will become familiar with all aspects of AWS&rsquo;s business, and interface directly with the business units in the region.
 
 
 Key job responsibilities
 
 
 This Riyadh-based Government Affairs And Policy Position, Which Will Also Participate In The Amazon Europe, Middle-East &amp; Africa Public Policy Team, Shall
 
 
 <ul>
 <li>
 Develop, lead and implement Saudi Arabia government affairs advocacy objectives and policy/political priorities for Amazon Web Services (AWS);
 </li>
 <li>
 Represent key policy positions directly and through industry associations to the governments and local authorities to enable a transparent and innovation friendly regulatory environment for the growth of AWS customers;
 </li>
 <li>
 Work collaboratively and transparently with the AWS business units to ensure alignment between core business priorities, public policy goals and &ldquo;go to market&rdquo; strategies;
 </li>
 <li>
 Assess and communicate potential regulatory issues and government sector market segment (revenue) opportunities and threats, develop mitigation or enhancement strategies and policy positions, and coordinate external advocacy efforts, outreach programs and key initiatives in concert with AWS business objectives;
 </li>
 <li>
 Facilitate high-level meetings between AWS executives and key stakeholders, including senior government officials, regulators, industry association and alliance partners to promote and advocate the company&rsquo;s public policies;
 </li>
 <li>
 Determine, maintain and staff appropriate corporate membership opportunities in industry associations on behalf of AWS, and ensure appropriate utilization of high judgment, high integrity outside consultants.
 
 
 </li>
 </ul>
 The successful candidate must be inquisitive, enthusiastic about technology, enjoy working hard and being continually challenged, and demonstrate sound judgment even in ambiguous situations. The responsibilities require that candidates be willing and able to make frequent trips, within Saudi Arabia and the Middle-East.
 
 
 
 Basic Qualifications
 
 
 
 <ul>
 <li>
 Relevant experience representing a large company or organization (e.g. trade or industry association) on policy advocacy and government affairs matters with policymakers and government stakeholders at the national and local levels.
 </li>
 <li>
 A Bachelor&rsquo;s degree in a relevant discipline (e.g. Law, Political Science, Public Policy, Public Affairs, Economic Development).
 </li>
 <li>
 Fluent in written and spoken English and Arabic.
 </li>
 <li>
 Maintain highest personal levels of ethical conduct, confidentiality and integrity, with a strong professional reputation in the industry.
 
 
 </li>
 </ul>
 
 Preferred Qualifications
 
 
 
 <ul>
 <li>
 Excellent understanding of the country&rsquo;s political landscape at a national, provincial and local level. Able to dive deep on political, legislative and regulatory trends that may impact AWS businesses, and to synthesize policy documents for internal and external customers.
 </li>
 <li>
 A strong understanding of IT issues in the country (such as cloud computing, Artificial Intelligence, cyber security, data protection, trade, taxes, and e-commerce).
 </li>
 <li>
 Demonstrated track-record of achieving meaningful changes to the legislative and regulatory environment through public policy advocacy.
 </li>
 <li>
 Highly effective oral, written and interpersonal communication skills. A strong track record of engaging with government ministries and agencies in ICT, financial services, health, energy regulators, and policy makers at the executive and working levels.
 </li>
 <li>
 Inquisitive, enthusiastic about technology, and able to demonstrate sound judgment in ambiguous situations.
 </li>
 <li>
 Effective research and analytical skills to develop and support policy positions.
 </li>
 <li>
 Effective time-management skills, including ability to prioritize and manage multiple workstreams.
 
 
 </li>
 </ul>
 Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you&rsquo;re applying in isn&rsquo;t listed, please contact your Recruiting Partner.
 
 
 
 
 Company
 
 - AWS EMEA SARL (Saudi Arabia Branch)
 
 
 Job ID: A2917696
</div>

Public Policy Manager, KSA, AWS Global Public Policy

Explore 1015+ Senior regulatory affairs specialist in Riyadh this October. Find roles across top companies and apply now to boost your career.

1015 senior regulatory affairs specialist jobs IN Riyadh

Senior Regulatory Affairs Specialist - GCL

Senior Regulatory Affairs Specialist - GCL

Regulatory Affairs Specialist (medical devices)

Regulatory Affairs Lead

Senior Coordinator - Permitting Office (Saudi National)

Policy Specialist

Public Policy Manager, KSA, AWS Global Public Policy