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PRANIC DRUG STORE LLC

Job Description We are seeking a Regulatory Pharmacist with strong experience in regulatory affairs and pharmacovigilance to join our team. The candidate must be fluent in Arabic and English and ensure compliance with all regulatory standards throughout the product lifecycle.Responsibilities<ul><li>Prepare, review, and submit regulatory documents to authorities.</li><li>Respond to regulatory queries and maintain compliance with regulatory requirements.</li><li>Support product registration, renewals, and variations.</li><li>Ensure pharmacovigilance reporting and documentation are completed accurately and on time.</li><li>Coordinate with internal teams to meet regulatory deadlines.</li></ul>Requirements<ul><li>Bachelor&rsquo;s degree in Pharmacy with valid license/eligibility (MOH).</li><li>Pharmacovigilance certificate (mandatory).</li><li>Minimum 1 years of experience in regulatory affairs.</li><li>Strong knowledge of regulatory standards and procedures.</li><li>Fluency in Arabic (mandatory) and English.</li><li>Preferably with own visa.</li><li>Valid UAE Driving Licence (preferred).</li></ul>Job Type: Full-time Location: United Arab EmiratesJob Type: Full-timePay: AED3,000.00 - AED10,000.00 per month

Regulatory Pharmacist (with Pharmacovigilance Certificate)

Huda Beauty

<div>
 
 Who We Are:
 
 At Huda Beauty, our Vision is to lead in creating a democratized beauty industry where power is given back to people to define, create, and enjoy beauty for themselves! Launched by award-winning beauty powerhouse Huda Kattan in 2013, Huda Beauty is one of the world's fastest-growing beauty brands. As a company, we are fueled by purpose and not profit, this allows us to approach things differently so that we can create products, content, and a community like no other. A lot has changed since our launch in 2013, but something that will forever remain at the core of Huda Beauty is our focus on business excellence and our unwavering passion for kindness!
 
 
 
 Summary:
 
 Reporting directly to the Regulatory Director, this role supports global regulatory compliance across all Huda Beauty brands. The ideal candidate is a team player with an autonomous, detail-oriented, results-driven working style, and the ability to juggle multiple projects and priorities in a fast-paced, entrepreneurial environment.
 
 
 
 Please note that this role is a 10-month fixed-term contract.
 
 
 
 
 Essential Duties and Responsibilities
 
 :
 
 
 <ul>
 <li>
 Support data collection and management of Regulatory led projects
 </li>
 <li>
 Work closely with Regulatory team (global &amp; regional) to ensure regulatory tasks and responsibilities are executed for all Huda Beauty brands
 </li>
 <li>
 Take the lead on regulatory requirements for new product development, including (but not limited to):
 </li>
 <li>
 Global formula &amp; packaging screening for regulatory compliance
 </li>
 <li>
 Ingredient lists, regulatory labelling requirements, and artwork reviews
 </li>
 <li>
 Organize testing and validation of product claims for marketing copy
 </li>
 <li>
 Liaising with product development and other global teams to ensure all regulatory elements are captured during development and execution
 </li>
 <li>
 Support Customer Services with all product inquiries &amp; adverse events
 </li>
 <li>
 Ensure timely execution of regulatory tasks and requirements related to certifications across all Huda Beauty brands
 </li>
 <li>
 Build and maintain Product Information Files (PIF) for all products, ensuring continuous updates and accuracy
 </li>
 <li>
 Help continue to drive process improvement within the Regulatory &amp; Compliance department
 </li>
 <li>
 Assist with drafting and obtaining signatures on letters where needed
 </li>
 <li>
 Manage confidential information with high discretion and demonstrate the highest levels of service and response time
 </li>
 <li>
 Stay abreast of global cosmetic regulatory updates
 
 
 </li>
 </ul>
 
 Requirements
 
 
 
 <ul>
 <li>
 Keen interest in the makeup and cosmetics industry
 </li>
 <li>
 Minimum of 2-3 years of experience in a Cosmetic Regulatory Affairs role
 </li>
 <li>
 Proficient in Microsoft Office (Excel, Word, PowerPoint, Outlook) and Adobe; familiarity with social media/web platforms is a plus
 </li>
 <li>
 Excellent attention to detail with an analytical mindset
 </li>
 <li>
 Strong organizational skills that reflect the ability to perform and prioritize multiple tasks seamlessly
 </li>
 <li>
 Strong interpersonal skills with the ability to collaborate and build relationships with internal and external stakeholders
 </li>
 <li>
 Demonstrated ability to achieve high-performance goals and meet deadlines in a fast-paced environment
 </li>
 <li>
 Forward thinker with a Kaizen (continuous improvement) mentality, who actively seeks opportunities to improve and proposes solutions
 </li>
 <li>
 Emotional maturity and intelligence
 </li>
 <li>
 Highly resourceful team player with the ability to be extremely effective independently
 </li>
 <li>
 Consistently display an approachable nature and flexible working style with flawless written &amp; verbal communication skills
 </li>
 <li>
 Strong presentation skills, with the ability to present to stakeholders at all levels of the organization when required
 </li>
 <li>
 Flexible working style, occasional early morning or late evening calls may be required to accommodate global business needs
 
 
 </li>
 </ul>
 
 Benefits
 
 
 
 <ul>
 <li>
 Monthly "Self Love Days" - at company discretion
 </li>
 <li>
 Premium Medical/Dental/Vision coverage for employee plus dependents
 </li>
 <li>
 Monthly coaching sessions with our in-house Success Coach
 </li>
 <li>
 Employee discounts on all Huda Beauty products
 </li>
 <li>
 Quarterly product gifting
 
 
 </li>
 </ul>
 
 Huda Beauty is committed to building diverse and inclusive teams and upholding an equal employment workplace that is free from discrimination. We hire stellar individuals regardless of their race, color, ancestry, religion, gender identity, national origin, sexual orientation, age, marital status, medical conditions, disability, or veteran status. If you need reasonable accommodations at any point in the application or interview process, please let us know.
 
</div>

Assistant Manager, Regulatory

<div>Who We Are: At Huda Beauty, our Vision is to lead in creating a democratized beauty industry where power is given back to people to define, create, and enjoy beauty for themselves! Launched by award-winning beauty powerhouse Huda Kattan in 2013, Huda Beauty is one of the world&rsquo;s fastest-growing beauty brands. As a company, we are fueled by purpose and not profit, this allows us to approach things differently so that we can create products, content, and a community like no other. A lot has changed since our launch in 2013, but something that will forever remain at the core of Huda Beauty is our focus on business excellence and our unwavering passion for kindness!
Summary: Reporting directly to the Regulatory Director, this role supports global regulatory compliance across all Huda Beauty brands. The ideal candidate is a team player with an autonomous, detail-oriented, results-driven working style, and the ability to juggle multiple projects and priorities in a fast-paced, entrepreneurial environment.
Please note that this role is a 10-month fixed-term contract.
Essential Duties and Responsibilities:<ul>
<li>Support data collection and management of Regulatory led projects
</li><li>Work closely with Regulatory team (global &amp; regional) to ensure regulatory tasks and responsibilities are executed for all Huda Beauty brands</li>
<li>Take the lead on regulatory requirements for new product development, including (but not limited to):</li>
<li>Global formula &amp; packaging screening for regulatory compliance</li>
<li>Ingredient lists, regulatory labelling requirements, and artwork reviews</li>
<li>Organize testing and validation of product claims for marketing copy</li>
<li>Liaising with product development and other global teams to ensure all regulatory elements are captured during development and execution</li>
<li>Support Customer Services with all product inquiries &amp; adverse events</li>
<li>Ensure timely execution of regulatory tasks and requirements related to certifications across all Huda Beauty brands</li>
<li>Build and maintain Product Information Files (PIF) for all products, ensuring continuous updates and accuracy</li>
<li>Help continue to drive process improvement within the Regulatory &amp; Compliance department
</li><li>Assist with drafting and obtaining signatures on letters where needed
</li><li>Manage confidential information with high discretion and demonstrate the highest levels of service and response time
</li><li>Stay abreast of global cosmetic regulatory updates</li>
</ul>Requirements<ul>
<li>Keen interest in the makeup and cosmetics industry</li>
<li>Minimum of 2-3 years of experience in a Cosmetic Regulatory Affairs role
</li><li>Proficient in Microsoft Office (Excel, Word, PowerPoint, Outlook) and Adobe; familiarity with social media/web platforms is a plus</li>
<li>Excellent attention to detail with an analytical mindset
</li><li>Strong organizational skills that reflect the ability to perform and prioritize multiple tasks seamlessly
</li><li>Strong interpersonal skills with the ability to collaborate and build relationships with internal and external stakeholders</li>
<li>Demonstrated ability to achieve high-performance goals and meet deadlines in a fast-paced environment
</li><li>Forward thinker with a Kaizen (continuous improvement) mentality, who actively seeks opportunities to improve and proposes solutions</li>
<li>Emotional maturity and intelligence
</li><li>Highly resourceful team player with the ability to be extremely effective independently</li>
<li>Consistently display an approachable nature and flexible working style with flawless written &amp; verbal communication skills</li>
<li>Strong presentation skills, with the ability to present to stakeholders at all levels of the organization when required
</li><li>Flexible working style, occasional early morning or late evening calls may be required to accommodate global business needs.</li>
</ul>Benefits<ul>
<li>Monthly &ldquo;Self Love Days&rdquo; &ndash; at company discretion</li>
<li>Premium Medical/Dental/Vision coverage for employee plus dependents</li>
<li>Monthly coaching sessions with our in-house Success Coach</li>
<li>Employee discounts on all Huda Beauty products</li>
<li>Quarterly product gifting</li>
</ul>Huda Beauty is committed to building diverse and inclusive teams and upholding an equal employment workplace that is free from discrimination. We hire stellar individuals regardless of their race, color, ancestry, religion, gender identity, national origin, sexual orientation, age, marital status, medical conditions, disability, or veteran status. If you need reasonable accommodations at any point in the application or interview process, please let us know.</div>

ATHGADLANG

Job OverviewWe are seeking a highly organized and detail-oriented PRO Services Specialist to manage all government-related processes and documentation with a strong emphasis on proposal drafting and submission. The ideal candidate will act as a liaison between the company and governmental authorities, ensuring timely and accurate processing of permits, licenses, and approvals. You will also be responsible for preparing well-structured proposals to support business initiatives and regulatory compliance.Key Responsibilities<ul><li>Prepare, draft, and submit official proposals, applications, and requests to relevant government departments and agencies.</li><li>Liaise with government authorities to facilitate approvals, renewals, and document clearances related to company operations.</li><li>Manage visa processing, labor permits, company registration, and other government-related documentation efficiently.</li><li>Ensure compliance with all legal and regulatory requirements in proposal preparation and submission.</li><li>Monitor and track the status of submitted proposals and documents to ensure timely follow-up and resolution.</li><li>Maintain organized records of all correspondences, permits, and proposal documents.</li><li>Provide advisory support to internal departments on government regulations and procedural requirements.</li><li>Collaborate with internal teams to gather necessary information and supporting documents for proposal submissions.</li><li>Draft clear and professional proposals tailored to the requirements of specific government bodies.</li><li>Identify opportunities to streamline the proposal and documentation process to improve efficiency.</li></ul>Qualifications &amp; Skills<ul><li>Proven experience as a PRO specialist, government liaison officer, or similar role.</li><li>Strong proficiency in proposal writing and documentation related to government approvals.</li><li>Excellent knowledge of local government regulations, labor laws, and visa procedures.</li><li>Strong communication and interpersonal skills to interact effectively with government officials and internal stakeholders.</li><li>High attention to detail with strong organizational and time management abilities.</li><li>Proficient in MS Office Suite (Word, Excel, PowerPoint) and document management systems.</li><li>Ability to work independently and handle multiple tasks under tight deadlines.</li><li>Fluency in [local language(s)] and English is preferred.</li></ul>Preferred Qualifications<ul><li>Degree or diploma in Business Administration, Public Administration, Law, or related field.</li><li>Prior experience working with government departments or regulatory bodies.</li><li>Familiarity with digital government portals and online application systems.</li></ul>Job Types: Full-time, Contract

PRO Services- Proposal Making- Business Development

Chimera Steel Contracting LLC

Key Responsibilities&middot; Manage all government-related documentation, including visas, work permits, labor contracts, Emirates ID, and renewals.&middot; Liaise with government entities such as the Ministry of Labor, Immigration, DED, RERA, Municipality, and other regulatory authorities.&middot; Ensure timely processing of trade licenses, tenancy contracts, Ejari, and real estate-related approvals.&middot; Keep track of deadlines for license renewals, visa expirations, and regulatory compliance requirements.&middot; Support employees in the processing of official documents such as medical tests, Emirates ID, and residency visas.&middot; Maintain accurate records of all government-related transactions and ensure confidentiality of company documents.&middot; Handle notarization, attestation, and legalization of documents when required.&middot; Stay updated with UAE labor laws, immigration rules, and real estate regulations to ensure full compliance.&middot; Represent the company professionally in all interactions with government officials and authorities.Required Skills &amp; Qualifications&middot; Minimum 3 years of proven experience as a PRO in the UAE, preferably within the Construction or development sector.&middot; Strong knowledge of UAE labor law, immigration procedures, and free zone/mainland regulations.&middot; Excellent communication skills in English and Arabic (written and verbal).&middot; Strong networking and relationship-building skills with government entities.&middot; High attention to detail and ability to work under strict deadlines.&middot; Proficient in MS Office and document management systems.&middot; Valid UAE driving license (preferred).Job Type: Full-timePay: From AED3,000.00 per month

RTC-1 Employment Services

The Role
 Position Title: Compliance Officer Employment Type: Full Time Salary: up to 5K AED all-inclusive depending on experience and qualifications Job Location: Dubai, UAE About the Client: A leading Dubai-based automotive services provider, delivering roadside assistance, car registration, replacement vehicles, logistics, and international driving permits since 2003. • Monitor day-to-day operations to ensure compliance with UAE laws, company policies, and industry regulations. • Maintain and update compliance records, reports, and documentation for audits and inspections. • Assist in reviewing contracts, internal procedures, and employee practices to ensure alignment with regulatory standards. • Support management in implementing compliance training, awareness, and reporting of potential risks or breaches.
 
Requirements
 <ul>
<li>Open to Asian nationals, 38 years old and below • Bachelor’s degree in Business Administration, Finance, or related field. • Minimum 2 years’ experience in compliance, audit, or administrative roles in the UAE. • Must have a strong understanding of UAE labor law and basic regulatory requirements.</li>
</ul>
About the company
 RTC-1 Employment Services is a licensed recruitment firm based in Dubai, UAE. Our team has been in the market since 2004 and we are supporting various industries with their staffing needs across the Middle East and Africa.

Compliance Officer

AstraZeneca

<div>JOB TITLE
Medical Director Gulf &ndash; OBU 
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 Medical Affairs Director for AZ Gulf is a key member of the Gulf Leadership Team, accountable for the strategic leadership and direction of the Medical Affairs function. You will ensure the highest standards of scientific, ethical, and medical expertise are applied in supporting the safe and effective use of AstraZeneca&rsquo;s medicines. The role leads collaboration with internal and external stakeholders to deliver evidence-based medical strategies, clinical insights, knowledge exchange, and scientific engagement.
The Medical Affairs Director will have a vital voice in shaping commercial, regulatory, and patient access strategies, ensuring alignment with global and regional objectives while maintaining a focus on the Gulf healthcare environment and patient needs.
Key Responsibilities<ul><li>
Develop and execute the local Medical Affairs strategy in alignment with regional and global strategic imperatives and AstraZeneca&rsquo;s science-led approach.</li><li>
Drive diagnostic strategy to support clinical decision-making and advance organizational objectives.</li><li>
Provide scientific advice and strategic guidance to internal stakeholders (Commercial, Market Access, Regulatory, Clinical Operations) to support decision-making and maximize patient benefit.</li><li>
Oversee the planning and execution of medical activities and programs, including investigator-initiated studies, real-world evidence generation, advisory boards, and scientific exchange events.</li><li>
Build, lead, and inspire a high-performing Medical Affairs team, ensuring robust performance management, talent development, and a culture of scientific excellence and compliance.</li><li>
Serve as the primary medical interface for key external experts, healthcare professionals, academic institutions, and patient advocacy groups, fostering trusted scientific relationships.</li><li>
Ensure the timely and compliant dissemination of medical and scientific information, consistent with local regulatory and ethical standards.</li><li>
Support the launch and lifecycle management of AstraZeneca&rsquo;s product portfolio by delivering relevant medical education, data generation, medical insights, and effective collaboration with global teams.</li><li>
Oversee review and approval of promotional and non-promotional materials, ensuring adherence to medical and regulatory standards.</li><li>
Maintain up-to-date awareness of scientific developments, clinical practice trends, and local healthcare regulations to anticipate impacts and drive appropriate internal adjustments.</li><li>
Ensure compliance with AstraZeneca policies, local regulatory requirements, and international codes governing medical activities.</li><li>
Represent AstraZeneca in key external medical and scientific forums, shaping the affiliate&rsquo;s reputation as a leader in science and patient care.</li></ul>
Critical Competencies
<ul><li>Medical Expertise: Applies advanced clinical knowledge and judgement to inform decision-making.</li><li>
Regulatory &amp; Compliance Acumen: Ensures all activities meet regulatory, ethical, and company standards.</li><li>
Strategic Leadership: Develops and executes strategic plans aligning business goals with patient needs.</li><li>
Communication &amp; Collaboration: Communicates complex medical concepts and builds effective partnerships.</li><li>
Clinical Development &amp; Oversight: Oversees clinical trials, monitors safety, and ensures data integrity.</li><li>
Decision Making &amp; Problem Solving: Makes evidence-based decisions and resolves complex issues.</li><li>
Patient Centricity: Prioritizes patient safety, quality care, and ethical practices in all actions.</li><li>
Innovation &amp; Change Management: Promotes innovative thinking and leads organizational change.</li></ul>
Essential for the role<ul><li>
Medical degree (MD, PharmD); postgraduate qualification is an advantage.</li><li>
Minimum of 8 years&rsquo; experience in Medical Affairs or related scientific roles within the pharmaceutical or biopharmaceutical industry, with at least 3 years in a leadership capacity.</li><li>
In-depth understanding of the local healthcare ecosystem, clinical practice, regulatory environment, and scientific trends within Gulf.</li><li>
Proven ability to engage and influence key opinion leaders, stakeholders, and decision-makers.</li><li>
Demonstrated expertise in leading medical strategy, scientific communication, and evidence generation.</li><li>
Excellent leadership, team management, and cross-functional collaboration skills.</li></ul>
Desirable for the role<ul><li>
Experience of working in a global organization, preferably within the pharmaceuticals industry, and knowledge of the drug development life cycle and commercial aspects of the industry</li><li>
Experience of working within a multi-disciplinary team and liaising with senior leaders</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>

Medical Director Gulf – OBU

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1089 regulatory affairs specialist jobs IN Dubai

Regulatory Pharmacist (with Pharmacovigilance Certificate)

Assistant Manager, Regulatory

Assistant Manager, Regulatory

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PRO

Compliance Officer

Medical Director Gulf – OBU