real estate consultant

sales consultant

senior property consultant

legal advisor

business consultant

regulatory affairs consultant

SEPHORA

Get AI-powered advice on this job and more exclusive features. Reporting to: Compliance & Master Data Director At Sephora, beauty is about feeling seen, valued, and empowered, individually and collectively. It is connecting deeply with others, celebrating diversity and inclusivity, unlocking your potential and making a difference every day. Together, we belong to something beautiful. Since its inception in 1969 in Limoges, France, and as part of the LVMH Group since 1997, Sephora has been disrupting the prestige beauty retail industry. Today, Sephora continues to break with convention to drive its mission: champion a world of inspiration and inclusion where everyone can celebrate their beauty. With 56,000 employees in 35 countries, we connect customers and beauty brands within the world's most passionate beauty community. With a curation of nearly 500 brands, and our own label, Sephora Collection, we offer the most unique and diverse range of products: fragrances, makeup, hair care, skincare and much more. You will excel and enjoy this position if you are ready to actively handle the following missions: <ul> <li>To enter data from various source documents into the computer system for processing, here on the Authorities online system related to suppliers and products.</li> <li>Notification of Sephora Own Brand and Exclusive brands- prepares source data for computer entry by compiling and sorting information from regulatory documents such as ingredients lists / excel sheets prepared by the brands.</li> <li>Establishing entry priorities from brands and suppliers.</li> <li>Enters data in the online systems by inputting alphabetic and numeric information on keyboard according to screen format of the online system.</li> <li>Maintains data entry requirements/complies with data integrity.</li> <li>Check completed work for accuracy.</li> <li>Lead times for product notifications.</li> <li>Store completed documents in designed locations.</li> <li>Maintain the registration tracking files with certificates numbers and validity dates.</li> <li>Help and Support on the labelling Back and Forth exchanges with the brands and creation of artworks.</li> </ul> Do not hesitate to apply if you have: <ul> <li>Bachelor's degree in science, pharmacy, regulatory affairs.</li> <li>1 to 2 years in regulatory affairs and cosmetic industry, preferably in retail or FMCG.</li> <li>Proficiency in planning tools (RELEX, SAP, Oracle, etc.) and Microsoft Excel/Power BI.</li> <li>Strong communication, cross-functional collaboration, and stakeholder management.</li> <li>Data input, Ownership & Execution Focus.</li> </ul> Here, you will find: <ul> <li>Community. In which authenticity is embraced, and the strength of our differences fuels our collective spirit.</li> <li>Culture of Empowerment. Learning & growth, that offers you the tools, space and opportunity to learn, innovate and lead.</li> <li>Work that Brings Fulfilment. From delighting clients every day, to inspiring our industry at large, every action makes a difference.</li> </ul> Join us and belong to something beautiful Seniority level <ul> <li>Internship</li> </ul> Employment type <ul> <li>Internship</li> </ul> Job function <ul> <li>Quality Assurance, Supply Chain, and Accounting/Auditing</li> </ul> Industries <ul> <li>Retail Apparel and Fashion, Retail Luxury Goods and Jewelry, and Retail</li> </ul><img src="https://www.jobg8.com/Tracking.aspx?2BLAx2Vk0CYck5gk%2fUkgz11tC%2bGacsqdg" width="0" height="0" />

Regulatory Affairs Trainee

<div>
 
 
 Reporting to:
 
 Compliance &amp; Master Data Director
 
 
 
 Location:
 
 Dubai, United Arab Emirates
 
 
 
 
 
 At Sephora, beauty is about feeling seen, valued, and empowered, individually and collectively. It is connecting deeply with others, celebrating diversity and inclusivity, unlocking your potential and making a difference every day. Together, we belong to something beautiful.
 
 
 
 
 
 Since its inception in 1969 in Limoges, France, and as part of the LVMH Group since 1997, Sephora has been disrupting the prestige beauty retail industry. Today, Sephora continues to break with convention to drive its mission: champion a world of inspiration and inclusion where everyone can celebrate their beauty.
 
 
 
 
 
 With 56,000 employees in 35 countries, we connect customers and beauty brands within the world&rsquo;s most passionate beauty community. With a curation of nearly 500 brands, and our own label, Sephora Collection, we offer the most unique and diverse range of products: fragrances, makeup, hair care, skincare... and much more.
 
 
 
 
 
 
 You will excel and enjoy this position if you are ready to actively handle the following missions:
 
 
 <ul>
 <li>
 To enter data from various source documents into the computer system for processing, here on the Authorities online system related to suppliers and products.
 </li>
 <li>
 Notification of Sephora Own Brand and Exclusive brands- prepares source data for computer entry by compiling and sorting information from regulatory documents such as ingredients lists / excel sheets prepared by the brands.
 </li>
 <li>
 Establishing entry priorities from brands and suppliers.
 </li>
 <li>
 Enters data in the online systems by inputting alphabetic and numeric information on keyboard according to screen format of the online system.
 </li>
 <li>
 Maintains data entry requirements/complies with data integrity.
 </li>
 <li>
 Check completed work for accuracy.
 </li>
 <li>
 Lead times for product notifications.
 </li>
 <li>
 Store completed documents in designed locations.
 </li>
 <li>
 Maintain the registration tracking files with certificates numbers and validity dates.
 </li>
 <li>
 Help and Support on the labelling Back and Forth exchanges with the brands and creation of artworks.
 </li>
 </ul>
 
 
 
 
 
 Do not hesitate to apply if you have:
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in science, pharmacy, regulatory affairs.
 </li>
 <li>
 1 to 2 years in regulatory affairs and cosmetic industry, preferably in retail or FMCG.
 </li>
 <li>
 Proficiency in planning tools (RELEX, SAP, Oracle, etc.) and Microsoft Excel/Power BI.
 </li>
 <li>
 Strong communication, cross-functional collaboration, and stakeholder management.
 </li>
 <li>
 Data input, Ownership &amp; Execution Focus.
 </li>
 <li>
 Collaborative Communication.
 </li>
 </ul>
 
 
 
 
 
 Here, you will find:
 
 
 <ul>
 <li>
 
 Community.
 
 In which authenticity is embraced, and the strength of our differences fuels our collective spirit.
 </li>
 <li>
 
 Culture of Empowerment
 
 . Learning &amp; growth, that offers you the tools, space and opportunity to learn, innovate and lead.
 </li>
 <li>
 
 Work that Brings Fulfilment.
 
 From delighting clients every day, to inspiring our industry at large, every action makes a difference.
 </li>
 </ul>
 
 
 
 
 
 Join us and belong to something beautiful
 
 
 
 
</div>

IQVIA

No visa or accommodation sponsorshipYou will be responsible for regulatory activities required at a country level for pharmaceutical products including maintenance and approvals, marketing authorization transfers, communication with the Health Authority, artwork approval, etc., ensuring regulatory compliance in the applicable market(s).As part of the IQVIA Global Regulatory Affairs department, you will be working with our clients, global pharmaceutical companies.JOB OVERVIEWEssential Functions<ol><li>Manage the local regulatory submission preparation in collaboration with internal and external stakeholders based on the agreed strategy for designated countries.</li><li>Submit submissions such as renewals, variations, new applications, filings, MAH transfers to the local Health Authority and EMA, and follow up on the local regulatory approval process for designated countries.</li><li>Preparation of local Product Labelling (e.g., SmPC, PIL) in local language for designated countries.</li><li>Artwork review and approval in client systems.</li><li>Manage multiple pharmaceutical products.</li><li>Act as subject matter expert in regulatory processes.</li><li>Acts as a Regulatory Team Leader on more complex projects which may include authoring of regulatory documentation and filling application forms.</li><li>Establishes relationships with customers; may meet face to face to discuss regulatory issues, present lessons learned, and discuss customer comments.</li><li>Acts as a Subject Matter Expert in Regulatory knowledge in Chemistry Manufacturing and Controls or Lifecycle Maintenance / Marketing Authorization Transfers/ Labeling/ Publishing.</li><li>Project budget management.</li><li>Give guidance to junior colleagues including feedback on the quality of technical documents and may assist in their training and development.</li><li>Possible exposure to present to clients on complex regulatory processes and bid defense meetings.</li><li>Act as reviewer for regulatory standard operating procedures.</li><li>Prepare and deliver internal regulatory training if required.</li></ol>MINIMUM REQUIRED EDUCATION AND EXPERIENCEExperience: Typically requires 8-10 years of prior relevant experience.Education: Masters Degree in Life Sciences or related discipline.Skills and Abilities:<ul><li>Good understanding of the Research and Development process (Chemistry Manufacturing & Controls) relevant regulatory guidelines.</li><li>Possesses specific regulatory or technical expertise.</li><li>Interpersonal communication (oral and written) and organization skills.</li><li>Ability to establish and maintain effective working relationships with coworkers, managers, and clients.</li><li>Demonstrates self-motivation and enthusiasm.</li><li>Ability to adapt quickly to a rapidly changing environment.</li><li>Knowledge of Maintenance of Marketing Authorization.</li><li>Experience of preparing variation renewal packages and artwork approvals.</li><li>Fluent in English and able to effectively communicate complex business language to those who speak English as a second language.</li><li>Must be fluent in Arabic.</li></ul>IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world. Learn more at<img src="https://www.jobg8.com/Tracking.aspx?%2fh34g3pSz%2f5vcg4ahaTk8lEKzSlsbq%2f%2bp" width="0" height="0" />

Global Regulatory Affairs Manager homebased

ANRA Technologies

Overview ANRA Technologies is seeking a Stakeholder Engagement and Regulatory Expert to support a strategic aviation project in the UAE in collaboration with DAEP, DANS, and the local civil aviation authority, alongside other civil and military airspace stakeholders. This is a dual-role position responsible for managing stakeholder engagement across government, regulatory, and operational bodies, while also providing technical regulatory guidance and compliance support for the project's successful execution. The ideal candidate will have a strong background in aviation regulation - particularly in U-space, UTM, and drone operations - with experience in working alongside both civil and military aviation authorities.Employment: Project-Based On-SiteCity: Dubai, United Arab EmiratesSchedule: Full TimeExperience: Min 7 yearsAbout ANRA: ANRA Technologies, with offices in Washington DC, London, New Delhi and Estonia, is an international provider of drone operations and traffic management solutions for unmanned aircraft systems (UAS) operators and airspace managers. We offer intelligent Machine Learning and AI driven traffic management software capabilities for UAS Traffic Management (UTM) and Urban Air Mobility (UAM) operations. Key Responsibilities <ul><li>Act as ANRA's primary liaison with the General Civil Aviation Authority (GCAA) and other relevant stakeholders including DAEP, DANS, defense entities, and airport operators</li><li>Build and maintain strong working relationships with civil and military authorities, attending coordination meetings and facilitating productive dialogue</li><li>Represent ANRA in stakeholder engagements, working groups, and regulatory consultations</li><li>Support joint planning sessions, workshops, and status reviews, ensuring alignment between technical teams and stakeholder expectations</li><li>Manage formal and informal communications with key government and regulatory counterparts</li></ul> Regulatory Support <ul><li>Provide regulatory interpretation and guidance for UTM/U-space implementation, including compliance with local drone regulations and airspace rules</li><li>Contribute to the development and submission of required documentation, such as Concept of Operations (ConOps), Letters of Agreement (LoA), safety assessments, and operational approvals</li><li>Track and interpret evolving UAE regulatory policies and frameworks, offering strategic input on how they impact project implementation</li><li>Coordinate with internal teams to ensure solution deployment aligns with applicable aviation, data protection, and cybersecurity regulations</li><li>Support the development of regulatory briefings, reports, and decision memos for internal and external stakeholders</li></ul> Required Qualifications <ul><li>Bachelor's or Master's degree in Aviation, Aerospace Engineering, Air Traffic Management, or related field</li><li>Minimum of 7 years of experience in the aviation industry with a focus on regulatory affairs, UTM/U-space, or air traffic management</li><li>Prior experience working with or liaising with civil aviation authorities, air navigation service providers, or defense entities in the UAE or GCC region</li><li>Deep knowledge of drone operations, U-space/UTM regulations, and manned aviation procedures</li><li>Strong stakeholder management and negotiation skills, especially in multicultural and high-level regulatory environments</li><li>Familiarity with international frameworks (e.g., ICAO, EASA, GCAA) and national regulatory processes</li><li>Excellent written and verbal communication skills</li></ul> Preferred Attributes <ul><li>Prior experience supporting aviation projects in the UAE or Middle East</li><li>Arabic language proficiency is a plus</li><li>Certification or training in aviation regulation, risk assessment, or safety management systems (SMS) is advantageous</li><li>Understanding of airspace modernization, C2/C3 frameworks, or joint civil-military operations</li></ul> What We Offer <ul><li>Competitive compensation and local benefits package</li><li>Opportunity to lead stakeholder engagement for a first-of-its-kind UTM/U-space project in the region</li><li>Exposure to high-impact aviation innovation in collaboration with major UAE aviation authorities</li><li>A dynamic, hands-on, and collaborative environment within a fast-paced global aviation software company</li></ul><img src="https://www.jobg8.com/Tracking.aspx?cVAb9OF4hnpBEW1GShW07%2fUTjwp%2brOYUz" width="0" height="0" />

Stakeholder Engagement and Regulatory Expert

ByteDance

<div>
 
 Responsibilities
 
 
 About the Team:
 
 Our legal team provides key support for all ByteDance&rsquo;s innovative initiatives, state-of-the-art products, and integrated platforms servicing our global video market. We help our technological and business teams enable their vision by providing integrated legal guidance and support. The ByteDance team is growing fast and is seeking highly experienced, bright and capable legal professionals to join the team. One of the critical challenges is the need for our team to provide exceptional legal support for the Data Privacy and Data Protection matters involving ByteDance. The following describes the responsibilities and requirements for the role.
 
 
 Responsibilities:
 
 - Provide data privacy legal support in the APAC and Emerging Markets (AEM) region with a focus on managing regulatory matters for the entire company and in over 120+ markets. This will include leading on regulatory investigations, litigation, government policy, external communications, et cetera.
 
 - Monitor privacy across markets to determine trends and issues for the company to address.
 
 - Coordinate internal communication, projects, and training amongst different teams.
 
 - Identify areas of common concern, redundancies in operation, and inefficiencies in order to develop standards and policies to improve workflow in the region.
 
 - Plan any other required activities so international and regional legal teams can meet their objectives and provide actionable deliverables to the company at large.
 
 - Merge solutions across key jurisdictions and their legal requirements with a focus on AEM but should have a foundational knowledge of other global laws (i.e. GDPR, CCPA, et cetera).
 
 - Increasingly advise on algorithmic and artificial intelligence-related matters.
 
 
 
 Qualifications
 
 
 Minimum Qualifications
 
 - Qualified to practice law and in good standing in UK, US, or other common law jurisdiction.
 
 - Significant experience managing privacy legal and regulatory matters
 
 - Experience working on data privacy efforts globally/regionally for a major multinational corporation or advising agency on data privacy issues.
 
 - Detail-oriented that can coordinate across multiple teams/countries.
 
 - Strong sense of problem-solving and proactive work ethic.
 
 - Determination to face tough challenges in a fast-paced environment while keeping a sense of humor.
 
 - Fluency in written and spoken English.
 
 
 Preferred Qualifications
 
 - Internationally recognized data privacy certifications or courses would be advantageous.
 
 - Demonstrated ability to lead / manage data privacy efforts globally / regionally
 
 - Experience, and more importantly personal interest, in technology, social network, internet, and all things digital is ideal.
 
 - Experience leading highly contentious and complex regulatory issues
 
 
 
 About Us
 
 
 Founded in 2012, ByteDance's mission is to inspire creativity and enrich life. With a suite of more than a dozen products, including TikTok, Lemon8, CapCut and Pico as well as platforms specific to the China market, including Toutiao, Douyin, and Xigua, ByteDance has made it easier and more fun for people to connect with, consume, and create content.&ZeroWidthSpace;
 
 
 
 
 Why Join ByteDance
 
 
 Inspiring creativity is at the core of ByteDance's mission. Our innovative products are built to help people authentically express themselves, discover and connect &ndash; and our global, diverse teams make that possible. Together, we create value for our communities, inspire creativity and enrich life - a mission we work towards every day.&ZeroWidthSpace;
 
 As ByteDancers, we strive to do great things with great people. We lead with curiosity, humility, and a desire to make impact in a rapidly growing tech company. By constantly iterating and fostering an "Always Day 1" mindset, we achieve meaningful breakthroughs for ourselves, our Company, and our users. When we create and grow together, the possibilities are limitless. Join us.&ZeroWidthSpace;
 
 Diversity &amp; Inclusion&ZeroWidthSpace;
 
 ByteDance is committed to creating an inclusive space where employees are valued for their skills, experiences, and unique perspectives. Our platform connects people from across the globe and so does our workplace. At ByteDance, our mission is to inspire creativity and enrich life. To achieve that goal, we are committed to celebrating our diverse voices and to creating an environment that reflects the many communities we reach. We are passionate about this and hope you are too.&ZeroWidthSpace;
</div>

Privacy Counsel (Regulatory), APAC & Emerging Markets

Amgen

Career Category Sales &amp; Marketing Operations Job Description HOW MIGHT YOU DEFY IMAGINATION? Live What you will do Let s do this. Let s change the world. In this vital role, you will manage country-specific regulatory affairs for Amgen's molecules, coordinate and implement regulatory submissions, ensure compliance with corporate and local requirements and lead documentation for local submissions under Senior Manager's guidance : <ul> <li> Ensures regulatory submissions are made on time and meet Amgen s corporate and local regulatory requirements </li> <li> With close supervision, implements the filing plan (MA and Lifecycle maintenance) for their countries, where applicable </li> <li> Reviews promotional and non-promotional materials </li> <li> Exchanges regulatory information and intelligence with other regulatory colleagues and cross functional teams on an ongoing basis and provides advice on local regulatory considerations/regulations in a timely manner </li> <li> Partners with Regulatory Affairs Lead to support the regulatory development, registration, and lifecycle management of all Amgen molecules </li> <li> Partners with peers to ensure consistency on procedures </li> <li> Assists locally in Healthcare Compliance activities, where applicable </li> <li> Participates in local regulatory process improvements, initiatives, and training </li> <li> Establishes regular contacts and interactions with Distributors (if applicable). </li> </ul> Win What we expect of you We are all different, yet we all use our unique contributions to serve patients. The Sr Regulatory Affairs professional we seek is a teammate with these qualifications. Preferred Qualifications: <ul> <li> Degree and in-depth regulatory experience of the Gulf Markets (1-2 years experience) </li> <li> Depth knowledge of regional countries legislation and regulations relating to medicinal products in the Gulf Markets. </li> <li> Experience interacting with regulatory agency in the Gulf markets </li> </ul> Thrive What you can expect of us As we work to develop treatments that take care of others, we also work to care for our teammates professional and personal growth and well-being. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com

Sr Congress & Events Coordinator

Peergrowth Consultancy Co.

We are seeking a detail-oriented and proactive Regulatory Affairs Coordinator to support regulatory activities at our UAE-based manufacturing facility. This role is responsible for compiling and coordinating product and site-specific regulatory dossiers for submission to global health authorities, including support for GMP audits. The ideal candidate will collaborate closely with Quality Assurance (QA), manufacturing, and technical teams at the site, as well as regional regulatory teams. Experience with local UAE and GCC regulatory requirements is preferred, with an understanding of global CTD requirements.KEY RESPONSIBILITIES<ul><li>Collate, compile, and review regulatory dossiers for product and site registrations in various international markets, including GMP audit dossiers.</li><li>Ensure accuracy, completeness, and regulatory compliance of all documentation submitted.</li><li>Review and verify the correctness and regulatory alignment of Artwork (AW) prior to submission.</li><li>Act as a key liaison between regional regulatory teams and site-based technical functions (QA, QC, Production, Engineering).</li><li>Coordinate technical responses and ensure timely resolution of queries raised by health authorities during or post submission through regional RA teams.</li><li>Maintain an organized and up-to-date archive of all regulatory submissions made from the site.</li><li>Implement proper version control, submission tracking, and document retrieval protocols.</li><li>Monitor submission timelines and follow up with internal teams to ensure timely completion of deliverables.</li><li>Ensure alignment with both international regulatory expectations and local UAE / GCC requirements.</li><li>Provide regular status updates on submissions and queries to the Head of International Regulatory Affairs.</li><li>Support documentation requests for internal audits, inspections, and compliance reviews.</li></ul>CANDIDATE EXPERIENCE<ul><li>Bachelors or masters degree in pharmacy (preferred)</li><li>2 to5 years of experience in Regulatory Affairs, ideally in a manufacturing or site-based setting within the pharmaceutical industry.</li><li>Preferred : Experience with handling guidelines of UAE Ministry of Health (MoHAP), GCC-DR, Oman, Bahrain, or other Gulf regulatory bodies.</li><li>Practical knowledge of CTD / eCTD dossier formats and GMP audit preparation.</li></ul>Key Skills and Competencies<ul><li>Strong communication, collaboration, and coordination skills across technical and regulatory functions.</li><li>High level of accuracy, attention to detail, and document management capabilities.</li><li>Ability to manage multiple priorities, meet deadlines, and adapt to dynamic regulatory requirements.</li><li>Proficient in Microsoft Office (Word, Excel, PowerPoint) and document control systems.</li><li>Proactive approach to problem-solving and handling regulatory queries.</li></ul>Coordinator • Dubai, United Arab Emirates<img src="https://www.jobg8.com/Tracking.aspx?zVcfVDlfDotLNFq0K%2b68Cho%2fqss4iFlXs" width="0" height="0" />

Regulatory Affairs Coordinator

Explore 1970+ Regulatory affairs consultant in Dubai this October. Find roles across top companies and apply now to boost your career.

1970 regulatory affairs consultant jobs IN Dubai

Regulatory Affairs Trainee

Regulatory Affairs Trainee

Global Regulatory Affairs Manager homebased

Stakeholder Engagement and Regulatory Expert

Privacy Counsel (Regulatory), APAC & Emerging Markets

Sr Congress & Events Coordinator

Regulatory Affairs Coordinator