regulatory compliance coordinator

Peergrowth Consultancy Co.

<p>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.</p><p><b>KEY RESPONSIBILITIES</b></p><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><p><b>CANDIDATE EXPERIENCE</b></p><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><p><b>Key Skills and Competencies</b></p><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><p>Coordinator • Dubai, United Arab Emirates</p>

Regulatory Affairs Coordinator

Alfa Laval

<div><div>Position Overview:<br>
We are seeking a detail-oriented and proactive Compliance Coordinator to oversee corporate compliance matters, with a strong focus on export control regulations. This role ensures the company&rsquo;s operations adhere to all applicable laws, regulations, and internal policies, particularly those governing international trade and export activities.</div><div></div><div>
Key Responsibilities:</div><ul><li><div>
Corporate Compliance:</div><ul><li><div>
Maintain and update corporate records, filings, and governance documents.</div></li><li><div>
Ensure compliance with statutory and regulatory requirements across jurisdictions.</div></li></ul></li><li><div>
Export Control:</div><ul><li><div>
Advise business units on export licensing, classification, and screening requirements.</div></li><li><div>
Conduct due diligence on customers, suppliers, and transactions to identify export control risks.</div></li><li><div>
Prepare and submit export license applications and maintain related documentation.</div></li><li><div>
Develop and deliver export control training to staff.</div></li></ul></li><li><div>
Risk Assessment &amp; Reporting:</div><ul><li><div>
Identify, assess, and mitigate compliance risks related to corporate and export activities.</div></li><li><div>
Investigate and report potential violations or incidents.</div></li><li><div>
Liaise with regulatory authorities and external auditors as needed.</div></li></ul></li><li><div>
Continuous Improvement:</div><ul><li><div>
Stay updated on changes in export control and corporate compliance regulations.</div></li><li><div>
Recommend and implement process improvements to enhance compliance effectiveness.</div></li></ul></li></ul><div>
Qualifications:</div><ul><li><div>
Bachelor&rsquo;s degree in law, Commercial Law, or related field.</div></li><li><div>
0-2 years&rsquo; experience in corporate compliance.</div></li><li><div>
Strong knowledge of international trade regulations and export control frameworks.</div></li><li><div>
Excellent organizational, analytical, and communication skills.</div></li><li><div>
Ability to work independently and collaboratively in a fast-paced environment.</div></li></ul></div>

Compliance Coordinator (UAE National)

Heartbeat Health

<div>
 Heartbeat Health is the leading virtual-first cardiovascular care company in the country, providing patients with convenient, high-quality heart care through a combination of telemedicine, diagnostics, and virtual care programs. By leveraging real-time data and AI-powered insights, Heartbeat Health empowers providers and patients with personalized treatment plans, reducing hospitalizations and improving long-term heart health outcomes. Heartbeat Health is redefining how cardiovascular care is delivered in the digital age, led by our medical group of cardiologists, advanced practitioners, nurses, and care coordinators.
 <br/>
 <br/>
 The Clinical Operations &amp; Compliance Coordinator is responsible for providing administrative and operational support to Heartbeat Health&rsquo;s clinical entities and provider network. This role plays a key part in maintaining regulatory compliance, supporting operational efficiency, and facilitating smooth coordination across Licensing, Business Operations, and Legal teams. The Coordinator will help uphold the company&rsquo;s standards of quality, compliance, and organizational excellence in delivering virtual cardiology care.
 <br/>
 <br/>
 <strong>
  About the Role:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   This is an entry-level position suited for a highly organized, detail-oriented individual seeking to develop foundational experience in healthcare operations and telehealth compliance. The Coordinator will work closely under the direction of the Senior Manager of Clinical Operations, and will assist with maintaining regulatory compliance, processing filings, and supporting day-to-day operational activities
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Operations Support &amp; Administration
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Provide day-to-day operational and administrative support for clinical professional licensing and related compliance functions
  </li>
  <li>
   Manage multiple concurrent administrative tasks and meet strict deadlines with accuracy and professionalism
  </li>
  <li>
   Maintain organized documentation and records related to provider licensing, credentialing, and regulatory compliance.
  </li>
  <li>
   Opportunity for data visualization, dashboards, and creating company-facing materials to showcase project status
  </li>
  <li>
   Serve as a central point of contact for internal requests related to clinical operations and compliance tasks
  </li>
  <li>
   Be onsite at the NYC office at least once a week to manage incoming and outgoing mail, supporting operational logistics
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Cross-Functional Collaboration
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Assist with the maintenance and monitoring of internal business operations records, learn the ins and outs of telehealth business models to support company success. Partner with Licensing, Business Operations, and Legal teams to ensure streamlined workflows and accurate recordkeeping
  </li>
  <li>
   Support ad hoc projects such as compliance reviews, quality assurance initiatives, and internal audits that improve operational efficiency, compliance processes, and provider experience
  </li>
  <li>
   Contribute to process documentation and continuous improvement initiatives within the Clinical Operations team
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  About You:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Public Health, Social Science, Business, or a related field
  </li>
  <li>
   1&ndash;2 years of experience in operations, compliance, or administrative support (internship experience accepted)
  </li>
  <li>
   Proficiency with standard business tools including Microsoft or Google suite
  </li>
  <li>
   Strong organizational skills with exceptional attention to detail
  </li>
  <li>
   Excellent written and verbal communication abilities
  </li>
  <li>
   Ability to manage multiple priorities in a dynamic and fast-paced environment
  </li>
  <li>
   Demonstrated initiative, reliability, and professional judgments
  </li>
  <li>
   Eagerness to learn and develop within a healthcare operations environment
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  About our Culture:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   We are mission-driven: we're revolutionizing the way cardiovascular care is delivered
  </li>
  <li>
   We are fast-paced &amp; agile: we move quickly, iterate often, and value experimentation
  </li>
  <li>
   We are remote-first: flexibility, autonomy, and trust are at the core of how we operate
  </li>
  <li>
   We care about diversity: diversity allows us to build an excellent patient experience
  </li>
  <li>
   We are an equal opportunity employer: we do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status
   <br/>
   <br/>
   <br/>
  </li>
 </ul>
 This position offers the opportunity to gain hands-on experience in healthcare operations, regulatory compliance, and multi-state corporate administration. The Clinical Operations &amp; Compliance Coordinator will receive guidance and mentorship from experienced leaders while developing a strong foundation in healthcare regulatory processes, licensing, and operational management.
 <br/>
 <br/>
 We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
</div>


Clinical Operations & Compliance Coordinator

RTC-1 Employment Services

The Role
<br><b>Position Title:</b> Legal & Compliance Coordinator Employment Type: Full Time Salary: up to 6K AED all-inclusive depending on experience and qualifications Job Location: Dubai, UAE About the Client: A legal consultancy agency in Dubai specializing in Real Estate practice Job Description: • Maintaining office procedures including the filing systems • Preparing reports by reviewing and analyzing commercial contracts, Legal Notices and Lease Contracts • Verifying and liaising with the Legal & Compliance department employees in operation aspect • Compiling detailed records of contract renewal, Legal Court Cases, licenses and regulatory deadlines
<br><br>
Requirements
<br><ul>
<li>Bachelors degree in Law or related field or Certificate of completion from an ABA-approved paralegal certification program of education and training or associate degree in paralegal studies • Proficient with Microsoft, basic AI tools • Fluent in speaking English ; Arabic is a plus • Must be 3 yr in Admin role in a legal firm / corporate set up.</li>
</ul>
About the company
<br>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.

Legal And Compliance Coordinator

Pfizer

<div><div>JOB SUMMARY</div><div>
Vault RIM process and system is highly dependent on accurate &amp; complete metadata at all levels and there is also an increasing amount of data that Health Authorities are requiring to be tracked and submitted.
</div><div>The Regulatory Data Coordinator is responsible for driving key &amp; critical activities within V-RIM in support of enabling the assessment and subsequent management of new or required changes (system events).</div><div>
They will specifically review all events initiated across the product lifecycle, completing system impact assessments, and creating Activities, Regulatory Objectives, Submissions to enable GRS to take the necessary actions. The Coordinator also ensures that Event Details, Change Items &amp; Label Concepts are associated and have the appropriate details as well as creating the Global Content Plan in readiness for content authoring across the enterprise.</div><div>
The Coordinator will work with the CMC Product strategist(s), labeling leads, Clinical &amp; Country Regulatory Strategists through a mix of strategic and operational support, demanding a detailed understanding of regulatory system structures, product licences &amp; master data as well as the end-to-end regulatory change management experience within &amp; across domains.</div><div></div><div>
JOB RESPONSIBILITIES</div><ul><li>
Management of all related RIM events and their related records, including event details and registered details &ndash; ensuring structures and relationships enable accurate reflection of the product market registration while still aligning to master data, and ensuring maintenance in alignment with agency decisions.</li><li>
HA Decision/Interaction management: Interpreting communications and drive appropriate actions to update system (and potentially notify stakeholders even if accountability for that remains with the Reg Strategist), collaborating with Stakeholders across GRS &amp; CMC strategists, PGS, and other teams to understand data requirements and ensure data needs are met.</li><li>
Review and Approve Data Changes: Evaluate and approve data change requests, ensuring compliance with data governance policies.</li><li>
Active Dossier Management: Ensuring maintenance across the lifecycle, including in alignment with agency decisions
</li><li>Provide Training and Support: Train &amp; support business users on data quality standards and data &amp; process management best practices.</li><li>
Serve as a major source of innovative ideas seeking future efficiencies and effectiveness whilst formulating new common optimum process in support of products through the development and commercial Lifecyle of a drug</li><li>
Ensure escalations, business process &amp; solution achieves business needs</li><li>
Evolve service based on strategic objectives &ndash; efficiency / quality drivers</li></ul><div></div><div>
Typical Tasks:</div><ul><li>
Collaboration and Communication: Work closely with business units, IT, and other stakeholders to understand data requirements and support data-related initiatives. Lead data review/update meetings. Provide guidance and support to system users through an advanced understanding.</li><li>
Notifications and Reporting: Ensure that notifications are sent to relevant stakeholders upon completion of data updates. Generate reports on data quality, data requests, and other relevant metrics.</li><li>
Review Event Information: Ensure understanding of the event's purpose and scope. Interpret and understand the change items to ensure appropriate event details are updated to enable proper impact assessments and GPC structure to be created.</li><li>
Create Event Details: Use the wizard to create event details, selecting appropriate actions and fields.</li><li>
Run Impact Assessment Report: Generate the report to identify impacted registrations.</li><li>
Create Related Records: Use the wizard to create activities and other related records based on the impact assessment report. Verify the records created by the wizard and confirm their accuracy. Check for any discrepancies and ensure all data is correctly entered and linked.</li><li>
Facilitates delivery and approval of Pfizer electronic and paper regulatory submissions through co-ordination and execution of CMC components to unique requirements and standards of each submission and national market.</li><li>
Through active management of status and expected deliverables, identifies risks and partners with regulatory strategists and relevant stakeholders to mitigate risks to quality and timeliness of CMC changes while ensuring status is accurately reflected at all times through maintenance of metadata in regulatory workflow and/or document management system(s).</li><li>
Contributes to the completion of moderately complex projects</li><li>
Manages own time to meet agreed targets; develops plans for short-term work activities on own projects (timelines, work plans, deliverables) within a Work Team</li><li>
Applies skills and discipline knowledge to contribute to the achievement of work within Work Team</li><li>
Makes decisions to resolve moderately complex problems in standard situations</li><li>
Makes decisions within guidelines and policies</li><li>
Participates and contributes as a team member</li></ul><div></div><div>
ORGANIZATIONAL RELATIONSHIPS</div><ul><li>
Regulatory Strategy, CMC leads, Clinical, Non-Clinical, Data Coordinators, RIO, Digital</li><li>
Will work in a highly matrixed environment and in close collaboration with Operations and Strategy.</li></ul><div></div><div>
RESOURCES MANAGED</div><ul><li>
Project specific resources &amp; vendor staff</li></ul><div></div><div>
QUALIFICATIONS / SKILLS</div><ul><li>
B.S./B.Scs. is in Pharmacy, Life Sciences, Business or Information Technology (desirable); equivalent relevant professional experience will be considered.</li><li>
2+ years of experience in regulatory, data management, data governance, or a related role within the pharmaceutical or healthcare industry.</li><li>
E2E global regulatory change management experience, including change initiation, performing impact assessments, submission to HA and management of HA decisions/queries/interactions/commitments
</li><li>Detailed understanding of regulatory system structures and how they are intended to enable regulatory business needs and support compliance</li><li>
Detailed understanding of regulatory SME processes and needs across the lifecycle, e.g. centralized registration procedures, IDMP, CMC, Artwork/Labeling</li><li>
Detailed understanding of GRS roles/responsibilities related to dossier maintenance and submissions
</li><li>Strong understanding of data governance principles and best practices.</li><li>
Experience with master data management and data quality improvement.</li><li>
Proven technical aptitude and ability to quickly learn and use new software, regulations and quality standards.</li><li>
Strong communication and collaboration skills.</li><li>
Attention to detail and commitment to data accuracy and integrity.</li></ul><div></div><div>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Regulatory Affairs</div><div></div>

Regulatory Data Coordinator, Senior Associate

<div>
 <strong>
  Job Summary
  <br/>
  <br/>
 </strong>
 Vault RIM process and system is highly dependent on accurate &amp; complete metadata at all levels and there is also an increasing amount of data that Health Authorities are requiring to be tracked and submitted.
 <br/>
 <br/>
 The Regulatory Data Coordinator is responsible for driving key &amp; critical activities within V-RIM in support of enabling the assessment and subsequent management of new or required changes (system events).
 <br/>
 <br/>
 They will specifically review all events initiated across the product lifecycle, completing system impact assessments, and creating Activities, Regulatory Objectives, Submissions to enable GRS to take the necessary actions. The Coordinator also ensures that Event Details, Change Items &amp; Label Concepts are associated and have the appropriate details as well as creating the Global Content Plan in readiness for content authoring across the enterprise.
 <br/>
 <br/>
 The Coordinator will work with the CMC Product strategist(s), labeling leads, Clinical &amp; Country Regulatory Strategists through a mix of strategic and operational support, demanding a detailed understanding of regulatory system structures, product licences &amp; master data as well as the end-to-end regulatory change management experience within &amp; across domains.
 <br/>
 <br/>
 <strong>
  Job Responsibilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Management of all related RIM events and their related records, including event details and registered details &ndash; ensuring structures and relationships enable accurate reflection of the product market registration while still aligning to master data, and ensuring maintenance in alignment with agency decisions .
  </li>
  <li>
   HA Decision/Interaction management: Interpreting communications and drive appropriate actions to update system (and potentially notify stakeholders even if accountability for that remains with the Reg Strategist) , collaborating with Stakeholders across GRS &amp; CMC strategists, PGS, and other teams to understand data requirements and ensure data needs are met.
  </li>
  <li>
   Review and Approve Data Changes: Evaluate and approve data change requests, ensuring compliance with data governance policies.
  </li>
  <li>
   Active Dossier Management: Ensuring maintenance across the lifecycle, including in alignment with agency decisions
  </li>
  <li>
   Provide Training and Support: Train &amp; support business users on data quality standards and data &amp; process management best practices.
  </li>
  <li>
   Serve as a major source of innovative ideas seeking future efficiencies and effectiveness whilst formulating new common optimum process in support of products through the development and commercial Lifecyle of a drug
  </li>
  <li>
   Ensure escalations, business process &amp; solution achieves business needs
  </li>
  <li>
   Evolve service based on strategic objectives &ndash; efficiency / quality drivers
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Typical Tasks:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Collaboration and Communication: Work closely with business units, IT, and other stakeholders to understand data requirements and support data-related initiatives. Lead data review/update meetings. Provide guidance and support to system users through an advanced understanding.
  </li>
  <li>
   Notifications and Reporting: Ensure that notifications are sent to relevant stakeholders upon completion of data updates. Generate reports on data quality, data requests, and other relevant metrics.
  </li>
  <li>
   Review Event Information: Ensure understanding of the event's purpose and scope. Interpret and understand the change items to ensure appropriate event details are updated to enable proper impact assessments and GPC structure to be created.
  </li>
  <li>
   Create Event Details: Use the wizard to create event details, selecting appropriate actions and fields.
  </li>
  <li>
   Run Impact Assessment Report: Generate the report to identify impacted registrations.
  </li>
  <li>
   Create Related Records: Use the wizard to create activities and other related records based on the impact assessment report. Verify the records created by the wizard and confirm their accuracy. Check for any discrepancies and ensure all data is correctly entered and linked.
  </li>
  <li>
   Facilitates delivery and approval of Pfizer electronic and paper regulatory submissions through co-ordination and execution of CMC components to unique requirements and standards of each submission and national market.
  </li>
  <li>
   Through active management of status and expected deliverables, identifies risks and partners with regulatory strategists and relevant stakeholders to mitigate risks to quality and timeliness of CMC changes while ensuring status is accurately reflected at all times through maintenance of metadata in regulatory workflow and/or document management system(s).
  </li>
  <li>
   Contributes to the completion of moderately complex projects
  </li>
  <li>
   Manages own time to meet agreed targets; develops plans for short-term work activities on own projects (timelines, work plans, deliverables) within a Work Team
  </li>
  <li>
   Applies skills and discipline knowledge to contribute to the achievement of work within Work Team
  </li>
  <li>
   Makes decisions to resolve moderately complex problems in standard situations
  </li>
  <li>
   Makes decisions within guidelines and policies
  </li>
  <li>
   Participates and contributes as a team member
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  ORGANIZATIONAL RELATIONSHIPS
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Regulatory Strategy, CMC leads, Clinical, Non-Clinical, Data Coordinators, RIO, Digital
  </li>
  <li>
   Will work in a highly matrixed environment and in close collaboration with Operations and Strategy.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  RESOURCES MANAGED
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Project specific resources &amp; vendor staff
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Qualifications / Skills
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   B.S./B.Scs. is in Pharmacy, Life Sciences, Business or Information Technology (desirable); equivalent relevant professional experience will be considered.
  </li>
  <li>
   2+ years of experience in regulatory, data management, data governance, or a related role within the pharmaceutical or healthcare industry.
  </li>
  <li>
   E2E global regulatory change management experience, including change initiation, performing impact assessments, submission to HA and management of HA decisions/queries/interactions/commitments
  </li>
  <li>
   Detailed understanding of regulatory system structures and how they are intended to enable regulatory business needs and support compliance
  </li>
  <li>
   Detailed understanding of regulatory SME processes and needs across the lifecycle, e.g. centralized registration procedures, IDMP, CMC, Artwork/Labeling
  </li>
  <li>
   Detailed understanding of GRS roles/responsibilities related to dossier maintenance and submissions
  </li>
  <li>
   Strong understanding of data governance principles and best practices.
  </li>
  <li>
   Experience with master data management and data quality improvement.
  </li>
  <li>
   Proven technical aptitude and ability to quickly learn and use new software, regulations and quality standards.
  </li>
  <li>
   Strong communication and collaboration skills.
  </li>
  <li>
   Attention to detail and commitment to data accuracy and integrity.
   <br/>
   <br/>
  </li>
 </ul>
 Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
 <br/>
 <br/>
 Regulatory Affairs
</div>


Venco Imtiaz Contracting Co

<p><b>Job Title: NOC Coordinator</b></p><p><b>Location: Dubai, UAE</b></p><p><b>Employment Type: Full-Time</b></p><p><b>Key Responsibilities:</b></p><ul><li>Coordinate with local authorities to obtain necessary permits, approvals, and clearances for construction projects.</li><li>Ensure that all projects comply with local regulations, building codes, and standards, including safety and environmental guidelines.</li><li>Handle the entire No Objection Certificate (NOC) process, including application preparation, submission, and follow-up with relevant authorities.</li><li>Communicate with utility companies (such as water, electricity, and telecommunications) to arrange for service connections, disconnections, and relocations as needed.</li><li>Manage and organize documentation required for regulatory submissions, including architectural plans, safety reports, and environmental assessments.</li><li>Liaise with government departments to schedule and facilitate inspections, site visits, and certifications required during various project stages.</li><li>Track and monitor the status of permits, NOCs, and other regulatory approvals to ensure timely completion and compliance.</li><li>Ensure the timely renewal and update of licenses, permits, and other necessary documentation to avoid project delays.</li><li>Assist in resolving any issues, concerns, or disputes that arise with local authorities or utility companies during the project lifecycle.</li><li>Maintain comprehensive records and documentation related to all NOCs, permits, and regulatory approvals, ensuring they are easily accessible and up-to-date for audit and compliance purposes.</li><li>Manage and process employee visas, work permits, residency applications, and renewals in compliance with UAE immigration laws</li><li>Facilitate complex medical / police procedures on event of death of any employee or next to kin.</li><li>Coordinate with government authorities for company registrations, trade licenses, and other legal requirements.</li><li>Facilitate communication and relations with various government departments, including labor, immigration, and municipal authorities.</li><li>Assist in resolving labor disputes and issues related to employee welfare and compliance with labor laws.</li><li>Prepare and submit necessary reports and documentation to government authorities as required by law.</li><li>Stay updated on changes in government regulations and ensure the company remains compliant with all legal requirements.</li></ul><p><b>Requirements:</b></p><ul><li>Bachelor's degree in Engineering, Business Administration or related field</li><li>Minimum 5+ years of experience in a similar role with in UAE.</li></ul><p>Job Type: Full-time</p><p>Application Question(s):</p><ul><li>What is your salary expectation?</li><li>Can you join immediately? If not, what is your notice period?</li></ul><p>Experience:</p><ul><li>construction: 5 years (Required)</li></ul>

NOC COORDINATOR

Search 10000+ Regulatory compliance coordinator jobs near you this December. New roles added regularly across leading industries. Apply today.

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Regulatory Data Coordinator, Senior Associate

NOC COORDINATOR