32 Legal Consultant jobs in Saudi Arabia

Job Title:
Legal Consultant

Job Location:
Riyadh, Saudi Arabia

Years of Experience:
5+ Years

Responsibilities:

• Developing policies, regulations, and procedures for organizations to align with organizational governance policies.
• Presenting the latest practices and developments in the field of governance to the internal company team.
• Ensuring compliance with standards and legal regulations.
• Implementing best practices in corporate governance.
• Solid experience in applying knowledge of legal analysis and principles to deliver the full scope of strategic legal advisory services in line with the firm's strategy, needs/situation.
• Having law firms and private sector experience will be an added advantage.
• Effective consultation and advisory skills that enable clients and help them build their confidence and skills to deal with complex and multi-jurisdictional legal issues.
• Ability to work independently with limited supervision as well as part of a multicultural team.
• Ability to drive change and to be flexible, open-minded with integrity.
• Demonstrated communication, interpersonal, writing, and analytical skills.
• Drafting and reviewing agreements, producing technically accurate quality standard work, drafting technically correct opinions, and reviewing the reports.
• Interpret and apply the theoretical legal knowledge so that it applies to practical business solutions.
• Prioritize work so that the deadlines can be met and is responsible for gathering the relevant information from various resources by using some effective research tools.
• Assist in the preparation and research of proposals and try to identify problems.
• Provides suggestions as well as creative ideas, thoughts, etc., in various discussions and builds creditability with clients and colleagues by communicating with them in an effective manner.
• Provides assistance in providing legal solutions to the problems that have cropped up and ensure that it is in compliance with the current laws.
• Responsible for maintaining all the legal records.

Qualifications:

• LLB degree from an accredited, top-tier law school (essential).
• English Language (essential).
• 5+ Years of experience in practicing law (essential).
• Excellent verbal and written communication skills.
• Licensed.

Required Skills:

• Should have the ability to analyze legal disputes, issues, and others.
• Should have strong communication skills and should be able to work independently.
• Should be able to convey complex information in a simple way and make sure that the presented information is precise.
• Should have a strong sense of attention to detail and should be able to complete the given tasks and requests promptly and accurately.
• Should be able to demonstrate a high level of diplomacy, motivation, and tact while carrying out duties.
• Should be updated with the current Saudi laws and should be able to interpret and implement them in the right situations.
• Good advising, monitoring, researching, and supervising skills would be a plus.

Eram Talent is seeking a Corporate Legal Consultant specializing in HR Laws to join our team in Saudi Arabia. In this role, you will provide expert legal advice and guidance on human resources matters, ensuring compliance with local labor laws and regulations while supporting the organization in its HR practices.

• Advise the organization on HR-related legal issues, including employee relations, contracts, and regulatory compliance.
• Draft and review employment contracts, policies, and procedures to align with Saudi labor laws.
• Conduct legal research and analysis on changes in HR laws and regulations, ensuring the company is up-to-date and compliant.
• Assist in the resolution of employee disputes and grievances, providing legal insights to support HR in mediation and negotiations.
• Ensure that the company’s HR practices are aligned with legal standards and best practices in the industry.
• Train HR personnel on legal compliance matters, enhancing their understanding of relevant laws.
• Collaborate with management to develop strategies to mitigate legal risks associated with HR operations.

• Qualified legal professional with a bachelor’s degree in Law or a related field.
• 3-5 years of experience in corporate law, with a focus on HR laws and regulations in Saudi Arabia.
• In-depth knowledge of local labor laws and HR compliance issues.
• Strong analytical skills and the ability to interpret complex legal documents.
• Excellent communication and interpersonal skills.
• Proven experience in contract drafting and review.
• Ability to work collaboratively with various departments within the organization.
• Fluency in Arabic and English is preferred.

Saleh Al-Ghamdi Law Firm (SG Law Firm) is a distinguished law firm based in Jeddah, Saudi Arabia. We deliver high-quality legal services in litigation, corporate, and advisory matters, with a strong commitment to professionalism, integrity, and client success.

We invite applications for a key position on our legal team:

Lawyer & Legal Consultant

Key Responsibilities:

• Represent clients before courts and competent authorities.
• Draft and review legal documents, contracts, and pleadings.
• Provide legal consultations across diverse practice areas.
• Conduct legal research and analyze applicable laws and regulations.
• Perform other tasks related to the role.

Requirements:

• Saudi nationality (mandatory).
• Bachelor's degree in Law from an accredited university.
• Valid license to practice law.
• Active membership with the Saudi Bar Association.
• Minimum 3 years of professional legal experience.
• Fluency in Arabic and English.

Preferred Skills & Competencies:

• Strong legal writing and drafting skills (especially in Arabic).
• Excellent research and analytical abilities.
• Ability to manage multiple cases and meet deadlines under pressure.
• Professional communication skills and client-oriented approach.
• High ethical standards and commitment to professional integrity.
• Teamwork, adaptability, and problem-solving mindset.
• Proficiency in Microsoft Office and legal research tools.

Location:

Jeddah | Full-time

How to Apply:

Please submit your application by filling out the official application form.

• Provide strategic legal advice to support business operations and decision-making.
• Ensure compliance with all applicable laws, regulations, and corporate policies.
• Develop and implement legal policies, procedures, and corporate governance frameworks.
• Draft, negotiate, and finalize various contracts, including commercial agreements and service contracts.
• Collaborate with cross-functional teams to ensure legal compliance and achieve strategic objectives.
• Conduct legal due diligence for new business opportunities and partnerships.
• Handle cross-border legal matters, including international contracts and trade regulations.
• Assist in handling regulatory compliance, licensing, and approvals. Assist in regulatory filings, business licensing, and corporate governance requirements.
• Provide guidance and support on corporate governance matters, including board meetings and governance structures.
• Provide legal support in mergers, acquisitions, and corporate restructuring.
• Monitor changes in legislation and regulations relevant to the organization's operations and proactively advise on potential impacts.
• Assist in drafting reports, legal opinions, and official correspondence.

Legal Consultant

Must have 5 years of experience in law firm in KSA.

The Legal Consultant is responsible for providing expert legal advice and guidance to management on various legal matters, ensuring the company's compliance with applicable laws and regulations, and protecting the organization's interests in all legal transactions.

JOINING DATE: IMMEDIATELY

Job Type: Full-time

Pay: ﷼9, ﷼10,000.00 per month

Life Unlimited.
At Smith+Nephew, we design and manufacture technology that takes the limits off living.

The
Regulatory Affairs Specialist
is responsible for ensuring timely product registration and sustained regulatory compliance across the MENA region, with a focus on Saudi Arabia. This role supports business continuity by securing licenses, handling regulatory submissions, and maintaining positive relationships with local health authorities.

What will you be doing?

• Secure timely registration of new products in accordance with strategic plans.
• Ensure uninterrupted market access through proactive license renewals and tender documentation support.
• Monitor and interpret new and existing regulations, ensuring business alignment and readiness.
• Manage post-market regulatory activities and documentation to uphold compliance.
• Identify and mitigate regulatory risks impacting product lifecycle or market access.
• Maintain positive relationships with health authorities and regulatory bodies across the region.
• Collaborate cross-functionally with Global RA, distributors, and commercial teams to streamline regulatory processes.
• Support regulatory activities for import permits and tender submissions.
• Maintain and update central regulatory databases and product information systems.
• Contribute to the development of regional regulatory strategies in alignment with global objectives.

What will you need to be successful?

• Bachelor's degree in Biomedical Engineering, Pharmacy, or a related
• Saudi Arabian nationality
• Minimum 1 year of experience in regulatory affairs for medical devices.
• Consistent track record in regulatory submissions and compliance with regional health authority requirements.
• In-depth knowledge of SFDA regulations and MENA regional requirements.
• Familiarity with Quality Management System requirements in accordance with ISO 13485 and Good Distribution Practice (GDP).
• Strong understanding of post-market surveillance obligations.
• Experience with product registration and documentation for the KSA market.
• Proficient in English (written and spoken)

You. Unlimited.
We believe in creating the greatest good for society. Our strongest investments are in our people and the patients we serve.

Inclusion and Belonging:
committed to welcoming, celebrating and thriving on diversity, learn more about our Employee Inclusion Groups on our website

Your Future:
annual bonus, company stock saving plan

Work/Life Balance:
paid volunteering hours, flexible approach

Your Wellbeing:
Employee Assistance Program

Flexibility:
possibility of working in hybrid model

Training:
Hands-On, Team-Customized

Extra Perks:
referral bonus, recognition program, mentoring program

Stay connected by joining our Talent Community.

We're more than just a company - we're a community Follow us on LinkedIn to see how we support and empower our employees and patients every day.

Check us out on Glassdoor for a glimpse behind the scenes and a sneak peek into
You. Unlimited.
, life, culture, and benefits at S+N.

Explore our website and learn more about our mission, our team, and the opportunities we offer.

Date posted: Sep 10, 2025

City: Riyadh

Country/Region: SA

Type of Contract: Full-time Employment / Unlimited

Job Requisition ID: 9758

Regulatory Affairs Specialist - KSA

Job Purpose

• The Regulatory Affairs Specialist focuses on ensuring that the organization meets all of the applicable regulations. Their goal is to ensure that new products meet certain requirements as set by Health Authorities.
• Regulatory Affairs Specialist ME is responsible for Saudi Arabia activities (KSA).
• Identifying all elements and actions necessary for registering and maintaining valid marketing authorizations in KSA.
• Collaboration with the local partners, local authorities and WRA in France.
• Coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals or registrations.
• Handle registrations of new products/sites/medical devices, pricing as well as maintaining life cycle of products in KSA, including renewals and variations.
• Ensure that all relevant regulations are fully met in dossiers, with the aim of complying with the requirements established by Health Authorities.
• Collaborates closely with the Department Head in all department related tasks and activities.
• Compile and prepare new products and manufacturing sites registration files for submissions to authorities in KSA as per Regulatory timelines.
• Cross functionality & collaboration with Global teams as well as all ME departments, provide regulatory support and guidance whenever required.

Role Responsibilities
Life-Cycle
management of products

• Pre-registration coordination with WRA and preparation of documentation for KSA to compile the product and manufacturing site files, Review/ Preparation/Submission of dossiers, fees, inquiries, answers to questions, approvals.
• Life-cycle management of products that includes new registrations, renewals/minor variation of both products and sites.
• Follow country specific procedures and SFDA guidelines in the KSA market.
• Coordination & liaising with WRA teams/distributors for preparation of all types of regulatory dossiers & local documentation.
• Preparation of price forms and related documentation for new product registration files.
• Liaising with WRA, agents and authorities for documentation submission and follow-up and keep track.
• To keep track of the registration status of products with submission, registration, expiry dates.

Regulatory Tasks

• Closely collaborate with the Head of the Department for all regulatory tasks.
• Monthly Reports, Correspondences/Mails, Scientific Office Renewal at the SFDA.
• Involved actively in the budget preparation of KSA Regulatory Affairs.
• Follow-up on regulatory guidelines and ensure sharing of regulatory information with all concerned.
• Reference standard submissions to the authorities.
• Helping the Supply Chain Department for tenders - preparation of documentation for institutional tender submissions.
• Actively involved in Regulatory Audits.

Regulatory Site Management

• For all activities related to KSA -WRA Portal, Ereca, Solaris, LSRIMS, Cosac.

Other Related Tasks

• Management/Organizing department supported conferences for Health Authorities in the ME countries.
• Liaise closely with agent and Health Authorities in KSA.
• Responsible for Change Controls for Variations for the ME region.
• Work as a deputy for the local responsible person for advertisement/promotional material.
• Deputy Local Responsible person for validation of Packaging Items.
• Cross collaboration with other ME departments.

Dimensions

• Geographical span: ME - KSA.
• Work with the ME Regulatory Lead to develop a detailed understanding of regulatory guidelines and technical requirements in KSA.
• Life cycle management of products, understanding of industry-specific regulations, audit procedures, and the ability to ensure compliance with regulatory standards.
• Work and support the KSA Regulatory Affairs team.
• Cross-functionality with other departments.
• Report to the Head of the Department.

Requirements
Educational
qualifications

• Bachelor's Degree in Pharmacy / Science.

Relevant Experience

• 3+ years of relevant pharmaceutical regulatory experience within a large multinational organization.
• Experience working in Saudi Arabia (preferred).
• Experience of working within a Global pharmaceutical company would be an advantage.

Skills & Personal Characteristics

• Good knowledge of the Regulatory environment and procedures in KSA.
• Sharp Regulatory Intelligence.
• Ability to work cross functional to resolve complex issues.
• Strategic thinker, innovative, able to drive multiple-simultaneous initiatives, able to work under pressure, team player.
• Multi-tasking, organized, Process & Result oriented, Focused, Problem solving, good judgment and decision-making capability.
• Excellent interpersonal, Negotiation and relationship building skills.
• Excellent interpersonal, communication & digital skills.
• Written and spoken fluency in English & Arabic (French is an added advantage).

Whatever your area of expertise, your work within the Servier Group helps advance therapeutic progress for the benefit of patients. You will be part of teams recognized for their scientific excellence and reach your full potential in a professional environment that encourages you to develop yourself. Tailor-made onboarding journeys, mobility opportunities, quality trainings, responsible management, team spirit. All this and more in a workplace focused on your well-being.

At Servier, we are committed to therapeutic progress to serve patient needs. We put the diversity of our employees as a source of richness for the fulfillment of this vocation.

Date posted: Sep 10, 2025

City: Riyadh

Country/Region: SA

Type of Contract: Full-time Employment / Unlimited

Job Requisition ID: 9758

Regulatory Affairs Specialist - KSA

.

Job Purpose

• The Regulatory Affairs Specialist focuses on ensuring that the organization meets all of the applicable regulations. Their goal is to ensure that new products meet certain requirements as set by Health Authorities.
• Regulatory Affairs Specialist ME is responsible for Saudi Arabia activities (KSA).
• Identifying all elements and actions necessary for registering and maintaining valid marketing authorizations in KSA.
• Collaboration with the local partners, local authorities and WRA in France.
• Coordinate and document internal regulatory processes, such as internal audits, inspections, license renewals or registrations.
• Handle registrations of new products/sites/medical devices, pricing as well as maintaining life cycle of products in KSA, including renewals and variations.
• Ensure that all relevant regulations are fully met in dossiers, with the aim of complying with the requirements established by Health Authorities.
• Collaborates closely with the Department Head in all department related tasks and activities.
• Compile and prepare new products and manufacturing sites registration files for submissions to authorities in KSA as per Regulatory timelines.
• Cross functionality & collaboration with Global teams as well as all ME departments, provide regulatory support and guidance whenever required.

Role Responsibilities

Life-Cycle management of products

• Pre-registration coordination with WRA and preparation of documentation for KSA to compile the product and manufacturing site files, Review/ Preparation/Submission of dossiers, fees, inquiries, answers to questions, approvals.
• Life-cycle management of products that includes new registrations, renewals/minor variation of both products and sites.
• Follow country specific procedures and SFDA guidelines in the KSA market.
• Coordination & liaising with WRA teams/distributors for preparation of all types of regulatory dossiers & local documentation.
• Preparation of price forms and related documentation for new product registration files.
• Liaising with WRA, agents and authorities for documentation submission and follow-up and keep track.
• To keep track of the registration status of products with submission, registration, expiry dates.

Regulatory Tasks

• Closely collaborate with the Head of the Department for all regulatory tasks.
• Monthly Reports, Correspondences/Mails, Scientific Office Renewal at the SFDA.
• Involved actively in the budget preparation of KSA Regulatory Affairs.
• Follow-up on regulatory guidelines and ensure sharing of regulatory information with all concerned.
• Reference standard submissions to the authorities.
• Helping the Supply Chain Department for tenders - preparation of documentation for institutional tender submissions.
• Actively involved in Regulatory Audits.

Regulatory Site Management

• For all activities related to KSA -WRA Portal, Ereca, Solaris, LSRIMS, Cosac.

Other related tasks

• Management/Organizing department supported conferences for Health Authorities in the ME countries.
• Liaise closely with agent and Health Authorities in KSA.
• Responsible for Change Controls for Variations for the ME region.
• Work as a deputy for the local responsible person for advertisement/promotional material.
• Deputy Local Responsible person for validation of Packaging Items.
• Cross collaboration with other ME departments.

Dimensions

• Geographical span: ME - KSA.
• Work with the ME Regulatory Lead to develop a detailed understanding of regulatory guidelines and technical requirements in KSA.
• Life cycle management of products, understanding of industry-specific regulations, audit procedures, and the ability to ensure compliance with regulatory standards.
• Work and support the KSA Regulatory Affairs team.
• Cross-functionality with other departments.
• Report to the Head of the Department.

Requirements

Educationalqualifications

• Bachelor's Degree in Pharmacy / Science.

Relevant Experience

• 3+ years of relevant pharmaceutical regulatory experience within a large multinational organization.
• Experience working in Saudi Arabia (preferred).
• Experience of working within a Global pharmaceutical company would be an advantage.

Skills & Personal characteristics

• Good knowledge of the Regulatory environment and procedures in KSA.
• Sharp Regulatory Intelligence.
• Ability to work cross functional to resolve complex issues.
• Strategic thinker, innovative, able to drive multiple-simultaneous initiatives, able to work under pressure, team player.
• Multi-tasking, organized, Process & Result oriented, Focused, Problem solving, good judgment and decision-making capability.
• Excellent interpersonal, Negotiation and relationship building skills.
• Excellent interpersonal, communication & digital skills.
• Written and spoken fluency in English & Arabic (French is an added advantage).

Whatever your area of expertise, your work within the Servier Group helps advance therapeutic progress for the benefit of patients. You will be part of teams recognized for their scientific excellence and reach your full potential in a professional environment that encourages you to develop yourself. Tailor-made onboarding journeys, mobility opportunities, quality trainings, responsible management, team spirit. All this and more in a workplace focused on your well-being.

At Servier, we are committed to therapeutic progress to serve patient needs. We put the diversity of our employees as a source of richness for the fulfillment of this vocation.

Company Description

Almarfa Medical is a leading organization dedicated to introducing the latest innovative medical products to specialty medical centers throughout Saudi Arabia. Our efforts are powered by a professional and highly qualified team of consultants and sales people. We operate as a full-service organization, facilitating collaboration between medical product manufacturers and hospitals across the Kingdom.

Job Purpose:

The Regulatory Affairs Specialist is responsible for ensuring that all medical devices marketed and distributed by Almarfa Medical
comply with the regulatory requirements of the
Saudi Food and Drug Authority (SFDA)
. The role focuses on the registration, renewal, and maintenance of medical device marketing authorizations, ensuring timely approvals and full regulatory compliance throughout the product lifecycle.

Job Title: Regulatory Affairs Specialist

Location: Riyadh, Saudi Arabia

Department: Regulatory Affairs

Reports To: Regulatory Affairs Manager

Key Responsibilities:

• Prepare, compile, and submit medical device registration dossiers in compliance with
  SFDA MDS-REQ-1
  , and related guidelines.
• Coordinate and communicate with SFDA reviewers during the submission and evaluation phases to address comments and provide clarifications.
• Manage the registration and licensing of new products, facilities, and importers in the
  GHAD system
  .
• Ensure proper documentation and compliance with SFDA requirements for labeling, bundling, classification, and post-market surveillance.
• Maintain and update the
  Medical Device Marketing Authorization (MDMA)
  and ensure timely renewals before expiration.
• Collaborate with manufacturers and principals to collect technical documentation, including technical files, QMS certificates, risk-management reports, and clinical evaluations.
• Review and verify compliance of Instructions for Use (IFU), packaging, and labeling with local regulatory standards.
• Monitor changes in SFDA regulations and communicate updates to internal teams and international partners.
• Support internal audits, ISO 13485:2016 compliance, and quality-management activities related to regulatory documentation.
• Keep detailed records of all submissions, approvals, and correspondences with SFDA.

Qualifications and Skills:

• Bachelor's degree
  in Pharmacy, Biomedical Engineering, Medical Sciences, or related field.
• Minimum
  2–4 years of experience
  in
  SFDA medical device registration
  or similar regulatory affairs role.
• Strong knowledge of
  SFDA Medical Device Interim Regulation
• Familiarity with ISO 13485
  and
  ISO 14971
  standards.
• Excellent written and verbal communication skills in
  English and Arabic
  .
• Strong organizational skills and attention to detail.
• Ability to manage multiple submissions and deadlines efficiently.

Preferred Attributes:

• Experience with cardiovascular, surgical, or oncology medical devices.
• Prior work in a multinational or authorized representative company.
• Proficiency in the
  SFDA GHAD platform
  and e-services.

Please send your CV to