marketing manager

account manager

compliance officer

hr manager

marketing associate

regulatory affairs manager

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

Global Regulatory Affairs Manager (homebased)

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

Regulatory Affairs Coordinator

Ormco

<div>
 
 Job Description
 
 
 
 Maximizes revenues from sales of the organization's products and/or services through a base of reseller partners in specific assigned channels and/or vertical markets.
 
 
 
 Job Requirements
 
 
 
 Business Development Manager MEA based out of Dubai, UAE will be responsible for identifying and onboarding new distributors in emerging geographies to support Nobel Biocare&rsquo;s regional expansion. The role includes overseeing distributor operations in key MEA markets (UAE, Kuwait, Lebanon, Azerbaijan, Morocco, and Iraq) to ensure alignment with the company&rsquo;s strategic and operational objectives.
 
 
 The Business Development Manager MEA for Nobel Biocare will play a pivotal role in driving strategic growth, market penetration, and customer acquisition within the assigned geographical scope. This dynamic position encompasses the management of key accounts to foster long-term partnerships and ensure high levels of customer satisfaction. The role also involves identifying and securing new customers across private, public, institutional, and dental service organization (DSO) segments, while leading competitive conversion initiatives by effectively communicating Nobel Biocare&rsquo;s unique value proposition.
 
 
 Accelerating further growth through Regulatory Affairs, the role will lead portfolio management responsibilities, including monitoring the regulatory status of existing products within the MEA region in close collaboration with the regional Regulatory Affairs (RA) team, and driving incremental growth through the registration of new innovations in coordination with global product management, as well as regional and global regulatory teams.
 
 
 Success in this role requires a strategic mindset, strong market insight, and the ability to collaborate effectively with cross-functional teams to deliver tailored solutions that meet evolving customer needs.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Distributor Management: Oversee the distributors in MEA (UAE, Kuwait, Lebanon, Azerbaijan, Morocco, Iraq), ensuring alignment with Nobel Biocare's operational plan and strategy.
 </li>
 <li>
 Geographical Expansion: Identify new distributors in countries approved in operational plan, define go-to-market for the country and secure successful launch with supporting roles in regulatory affairs, marketing, etc.
 </li>
 <li>
 Portfolio Management: Monitor the regulatory status of existing products across all MEA countries in collaboration with the regional Regulatory Affairs (RA) team and manage the registration of new innovations throughout the MEA region in coordination with global product management, as well as regional and global regulatory teams.
 </li>
 <li>
 Account Management: Manage key accounts for Nobel Biocare within the assigned geographical scope, ensuring strong customer relationships and a high level of satisfaction.
 </li>
 <li>
 Customer Acquisition: Identify and acquire new customers across the private, public, institutional, and dental service organization (DSO) segments, expanding the market presence of Nobel Biocare.
 </li>
 <li>
 Competitive Conversion: Drive competitive conversions by effectively communicating the value proposition of Nobel Biocare products to end users.
 </li>
 <li>
 Value Proposition: Delivery of the full value proposition of Nobel Biocare with the support of the regional marketing, training and education and other supporting functions.
 </li>
 <li>
 Operational Implementation: Implement Nobel Biocare's operational plan and strategy within the region.
 
 
 </li>
 </ul>
 
 Training And Support
 
 
 
 <ul>
 <li>
 Deliver comprehensive training, education, and onboarding sessions, including face-to-face visits and technical support, to customers and local teams for Nobel Biocare.
 </li>
 <li>
 Expedite and ensure the efficient resolution of customer inquiries and service requests.
 </li>
 <li>
 Organize and manage promotional and technical follow-up interactions with healthcare professionals.
 </li>
 <li>
 Deliver extensive customer support through various communication platforms, including phone, email, and remote channels.
 
 
 </li>
 </ul>
 
 Sales And Performance
 
 
 
 <ul>
 <li>
 Achieve and exceed monthly, quarterly, and annual sales targets.
 </li>
 <li>
 Demonstrate a proven ability to convert key business from competitors to Nobel Biocare products.
 </li>
 <li>
 Provide technical support for surgical products, biomaterials and our digital portfolio.
 </li>
 <li>
 Conduct remote onboarding sessions for new and existing healthcare professionals.
 
 
 </li>
 </ul>
 
 Corporate Compliance
 
 
 
 <ul>
 <li>
 Follow corporate policies regarding customer entertainment and relations.
 </li>
 <li>
 Understand and support the company's policies and procedures to provide effective customer support.
 
 
 </li>
 </ul>
 
 Qualifications &amp; Expereince
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree or equivalent required (Dental/Oral Health/Science/technical background highly regarded)
 </li>
 <li>
 Demonstrated expertise in sales management, with a preference for +5 years of experience within the medical or dental sectors.
 </li>
 <li>
 Comprehensive knowledge of Nobel Biocare products and their unique value proposition.
 </li>
 <li>
 Exceptional skills in communication, training, and customer service.
 </li>
 <li>
 Proven ability to effectively manage multiple accounts and distributor relationships.
 </li>
 <li>
 Advanced proficiency in technical support and digital tools.
 </li>
 <li>
 Fluency in English and Arabic is required; proficiency in French is considered an asset.
 
 
 </li>
 </ul>
 
 Soft Skills
 
 
 
 <ul>
 <li>
 Communication: Excellent organizational and follow-up skills, with the ability to effectively communicate and persuade.
 </li>
 <li>
 Customer Service: Efficient problem-solving and responsiveness to customer inquiries.
 </li>
 <li>
 Team Collaboration: Ability to work effectively with cross-functional teams and adapt in a dynamic environment.
 </li>
 <li>
 Engagement: Strong engagement qualities to inspire and guide team members.
 </li>
 <li>
 Adaptability: Flexibility to navigate and thrive in a dynamic and changing environment.
 </li>
 <li>
 Time Management: Effective time management skills to prioritize tasks and meet deadlines.
 
 
 </li>
 </ul>
 
 Operating Company
 
 
 
 Ormco
 
 
 Ormco is a global leader and innovator of high-quality orthodontic products and solutions, including brackets and wires. For more than 60 years, our team has partnered with the orthodontic community to help create over 20 million smiles in more than 140 countries. We build trusted relationships. Each one is rooted in respect and understanding. We take that approach when we help orthodontists achieve their clinical and practice management objectives. We take the same approach when we help our team bring their personal best to work each day, ready to make a difference and reach their full potential.
 
 
 Envista and its family of companies (Envista) will not accept unsolicited resumes from any source other than directly from a candidate. Envista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening. Envista will not pay a fee to any Agency that does not have such agreement and written approval in place.
</div>

Business Development Manager, Nobel Biocare - MEA

<div>Site Name: UAE - Dubai 
Posted Date: Oct 23 2025 
Position Summary: 
We are inviting UAE Nationals to join our Regulatory Affairs team in the United Arab Emirates as a Regulatory Affairs Associate. This role is crucial in ensuring compliance with local regulations while supporting product lifecycle management and regulatory submissions. You&rsquo;ll collaborate with cross-functional teams to align regulatory strategies with business goals and contribute to meaningful work that improves lives.
Key Responsibilities: 
In this role, you will have the opportunity to develop your career while leading key activities such as:<ul><li>
Preparing, coordinating, and submitting regulatory documents in compliance with local regulations and GSK standards.</li><li>
Ensuring timely submissions and approvals to support product launches and lifecycle maintenance.</li><li>
Collaborating with internal teams and external stakeholders to align regulatory strategies with business objectives.</li><li>
Maintaining regulatory databases and ensuring accurate record-keeping in line with compliance requirements.</li><li>
Monitoring changes in local regulations and ensuring adherence to applicable laws and guidelines.</li><li>
Providing regulatory guidance to cross-functional teams to support business operations.</li></ul>
Basic Qualifications: 
To be successful in this role, you should have the following qualifications:<ul><li>
UAE National.</li><li>
Bachelor&rsquo;s degree in pharmacy, Medicine, or a related field.</li><li>
Proficiency in Microsoft Office tools (Word, Excel, PowerPoint).</li><li>
Strong attention to detail and organizational skills.</li><li>
Effective communication skills, both written and verbal.</li><li>
Ability to work collaboratively in a team environment.</li></ul>
Preferred Qualifications: 
We value candidates who bring additional skills and characteristics, such as:<ul><li>
Previous experience in regulatory affairs or a related field.</li><li>
Familiarity with regulatory submission processes and local guidelines.</li><li>
Strong problem-solving skills and the ability to prioritize tasks effectively.</li><li>
Interest in the pharmaceutical industry and regulatory compliance.</li><li>
Ability to adapt to a fast-paced and dynamic work environment.</li><li>
Commitment to continuous learning and professional development.</li></ul>
Additional Information: 
This role is based on-site in the United Arab Emirates. GSK is an equal opportunity employer and values diversity, equity, and inclusion. We welcome applications from UAE Nationals who are passionate about improving lives and ensuring compliance with local regulations.
Application Process: 
If you&rsquo;re ready to grow your skills, make a positive impact, and contribute to GSK&rsquo;s mission, apply today!
Why GSK? 
Uniting science, technology and talent to get ahead of disease together.
GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases &ndash; to impact health at scale.
People and patients around the world count on the medicines and vaccines we make, so we&rsquo;re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.
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>

Regulatory Affairs Associate

Amgen

Associate Regulatory Affairs - based in Dubai Join to apply for the Associate Regulatory Affairs - based in Dubai role at Amgen.You've worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals? At Amgen, our shared mission-to serve patients-drives all that we do. It is key to our becoming one of the world's leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role. 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>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 International Regulatory Leads (IRLs) and Global Regulatory Leads (GRLs) to support the regulatory development, registration, and lifecycle management of all Amgen molecules.</li><li>Partners with peers to ensure consistency on procedures.</li></ul> What We Expect Of You We are all different, yet we all use our unique contributions to serve patients. The Regulatory Affairs professional we seek is a teammate with these qualifications. Basic Qualifications <ul><li>Bachelor's degree in Pharmaceutical Science</li><li>Working with policies, procedures and SOPs.</li><li>Comprehensive understanding of regulatory activities and how they impact other projects and/or processes.</li><li>Knowledge of the Gulf legislation and regulations.</li><li>Understanding of regulatory activities and how they impact other projects and/or processes.</li><li>Understanding of drug development.</li><li>Demonstrate ability to work in teams.</li><li>Ability to understand and communicate scientific/clinical information.</li></ul> Preferred Qualifications <ul><li>Regulatory experience of the Gulf Markets.</li><li>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> 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 at Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Associate Regulatory Affairs - based in Dubai

Vivandi

Industry: Haircare | Hair loss | Supplements | Nutrition | FMCGPosition Summary:The Regulatory Specialist will be responsible for managing and ensuring compliance with all applicable regulatory requirements in the United Arab Emirates (UAE) and Kingdom of Saudi Arabia (KSA). The role involves handling product registration, documentation, labeling, and regulatory approvals for Haircare, Hair loss, Nutrition, Supplements, and FMCG products. The incumbent will work closely with internal departments and regulatory authorities to facilitate smooth market entry and continuous compliance.Key Responsibilities:<ul><li>Manage and oversee the product registration process with relevant regulatory authorities such as Dubai Municipality (DM), Emirates Authority for Standardization and Metrology (ESMA), Ministry of Health and Prevention (MOHAP), Saudi Food and Drug Authority (SFDA), Saudi Standards, Metrology and Quality Organization (SASO), and Gulf Standardization Organization (GSO).</li><li>Prepare, compile, and maintain regulatory dossiers and technical documentation for new and existing products.</li><li>Ensure all product formulations, claims, and ingredients comply with UAE and KSA regulations.</li><li>Review and approve product labels, artworks, and promotional materials for regulatory compliance.</li><li>Coordinate with internal teams including Research &amp; Development (R&amp;D), Quality Assurance, Marketing, and Supply Chain to ensure timely submission and maintenance of documentation.</li><li>Monitor and interpret regulatory updates, standards, and guidelines issued by UAE and Saudi authorities, advising management on necessary actions.</li><li>Support import clearance processes and ensure all compliance documentation is accurate and up to date.</li><li>Maintain a database of registered products, licenses, and renewal timelines to ensure continuous market authorization.</li><li>Provide regulatory guidance during new product development (NPD) and reformulation projects.</li><li>Ensure compliance with Good Manufacturing Practices (GMP), Gulf Cooperation Council (GCC), and Halal certification requirements applicable to the product categories.</li><li>Liaise with consultants, distributors, and third-party agencies involved in the regulatory process across both markets.</li></ul>Qualifications and Experience:<ul><li>Bachelor&rsquo;s Degree in Pharmacy, Chemistry, Biotechnology, or a related scientific discipline.</li><li>Minimum 3&ndash;5 years of experience in Regulatory Affairs within the Haircare, Nutrition, Supplements, or FMCG industries.</li><li>Comprehensive knowledge of UAE and KSA regulatory systems, procedures, and documentation requirements.</li><li>Proven experience in product registration, labeling compliance, and import documentation for cosmetics, personal care, or nutritional products.</li><li>Strong understanding of SFDA, DM, ESMA, SASO, and GSO frameworks and processes.</li><li>Excellent communication and coordination skills with government authorities and internal stakeholders.</li><li>High attention to detail, strong organizational skills, and the ability to manage multiple projects simultaneously.</li><li>Proficiency in English &amp; Arabic is mandatory.</li></ul>Key Competencies:<ul><li>Regulatory Documentation and Dossier Management</li><li>Analytical and Problem-Solving Skills</li><li>Strategic and Proactive Regulatory Planning</li><li>Stakeholder Management</li><li>Compliance and Risk Awareness</li><li>Adaptability and Process Orientation</li></ul>Job Type: Full-timePay: AED6,000.00 - AED8,000.00 per month

Regulatory Affairs Specialist

SEPHORA

<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>

Regulatory Affairs Trainee

Explore 2557+ Regulatory affairs manager in Dubai this November. Find roles across top companies and apply now to boost your career.