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governmental affairs specialist

Nawy

<div>
 The Governmental Affairs Specialist at Nawy Real Estate will play a crucial role in engaging with governmental bodies and regulatory agencies. This position entails monitoring policy developments, advocating for the company's interests, and ensuring compliance with relevant laws and regulations.
 <br/>
 <br/>
 <strong>
  Key Responsibilities:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Monitor and analyze legislative and regulatory developments that may impact Nawy's operations
  </li>
  <li>
   Develop and maintain strong relationships with governmental officials, industry associations, and other stakeholders
  </li>
  <li>
   Prepare reports and position papers to inform senior management on key issues impacting the business
  </li>
  <li>
   Coordinate with internal teams to ensure consistent messaging and strategic alignment in advocacy efforts
  </li>
  <li>
   Assist in the development and execution of governmental affairs strategies and initiatives that align with Nawy's business goals
  </li>
  <li>
   Represent Nawy at meetings, conferences, and public hearings to advocate for policies beneficial to the company
  </li>
  <li>
   Facilitate communication between Nawy and various governmental entities
  </li>
  <li>
   Prepare advocacy materials, policy briefs, and presentations for stakeholders
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Requirements
  <br/>
  <br/>
 </strong>
 <strong>
  Requirements:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor's degree in Political Science, Law, Public Affairs, or a related field
  </li>
  <li>
   2-4 years of experience in governmental affairs, public policy, or a similar role, preferably within the real estate industry
  </li>
  <li>
   Strong understanding of the legislative process and governmental structures
  </li>
  <li>
   Excellent communication and interpersonal skills, with the ability to build relationships with a variety of stakeholders
  </li>
  <li>
   Proven ability to analyze policy issues and communicate complex ideas effectively
  </li>
  <li>
   Strong organizational and time management skills, with the ability to manage multiple tasks concurrently
  </li>
  <li>
   Proficiency in Microsoft Office Suite and familiarity with CRM systems
  </li>
  <li>
   Ability to work independently and collaboratively within a team
  </li>
 </ul>
</div>


Governmental Affairs Specialist

Nawy Real Estate

<div><p>The Governmental Affairs Specialist at Nawy Real Estate will play a crucial role in engaging with governmental bodies and regulatory agencies. This position entails monitoring policy developments, advocating for the company's interests, and ensuring compliance with relevant laws and regulations.</p><p><b>
Key Responsibilities:</b></p><ul>
<li>Monitor and analyze legislative and regulatory developments that may impact Nawy&rsquo;s operations.</li>
<li>Develop and maintain strong relationships with governmental officials, industry associations, and other stakeholders.</li>
<li>Prepare reports and position papers to inform senior management on key issues impacting the business.</li>
<li>Coordinate with internal teams to ensure consistent messaging and strategic alignment in advocacy efforts.</li>
<li>Assist in the development and execution of governmental affairs strategies and initiatives that align with Nawy's business goals.</li>
<li>Represent Nawy at meetings, conferences, and public hearings to advocate for policies beneficial to the company.</li>
<li>Facilitate communication between Nawy and various governmental entities.</li>
<li>Prepare advocacy materials, policy briefs, and presentations for stakeholders.</li><br>
</ul><br>
<br>
<b>Requirements</b><p><b><br>
Requirements:</b></p><ul>
<li>Bachelor's degree in Political Science, Law, Public Affairs, or a related field.</li>
<li>2-4 years of experience in governmental affairs, public policy, or a similar role, preferably within the real estate industry.</li>
<li>Strong understanding of the legislative process and governmental structures.</li>
<li>Excellent communication and interpersonal skills, with the ability to build relationships with a variety of stakeholders.</li>
<li>Proven ability to analyze policy issues and communicate complex ideas effectively.</li>
<li>Strong organizational and time management skills, with the ability to manage multiple tasks concurrently.</li>
<li>Proficiency in Microsoft Office Suite and familiarity with CRM systems.</li>
<li>Ability to work independently and collaboratively within a team.</li></ul></div>

Organon Pharmaceuticals

<p></p><div><p><b>Job Title</b>: Assoc. Dir, Medical Affairs</p><p></p><p><b>
Location / Site</b>: Cairo</p><p></p><p><b>
The Position
</b></p><p></p><p>The Medical Advisor holds primary responsibility within the country for the development and execution of the Medical Affairs Plans in his/her therapeutic areas under the guidance and supervision of the META Cluster Medical Lead. Additionally, the Medical Advisor provides Medical Affairs therapeutic area support through engaging with Scientific Leaders (SLs) / Key Decision Makers (KDMs), driving scientific initiatives and supporting the field force.</p><p></p><p><b><br>
Responsibilities</b></p><p></p><p><i>
Scientific and Technical Leadership</i></p><p></p><ul><li>Communicate scientific therapy needs credibly, appropriately, and effectively across a variety of internal and external stakeholders at all levels.</li><li>Build trust with the external scientific community via peer-to-peer scientific exchange, research and educational collaborations, interactions with scientific societies and health organizations, publications, etc.</li><li>Provide therapeutic/functional training to assigned teams and affiliate functions.</li><li>Develop and help execute country medical educational programs and symposia.</li><li>Lead country Advisory Boards and Expert Input Forums in line with strategy.</li><li>Participate in and contribute significantly to professional organizations, academic or regulatory working teams.</li><li>Provide scientific inputs for digital initiatives.</li></ul><p></p><p><i>
Medical Strategy and Therapy Leadership</i></p><p></p><ul><li>Translate Global Medical Strategies into research, data analysis, scientific communication, educational, and other tactics and solutions that improve patient outcomes and enhance access in the country.</li><li>Ensure effective communication and collaboration between field and Medical through providing scientific and medical support to the Commercial team.</li><li>Evaluate accuracy of promotional materials.</li><li>Provide Medical Affairs therapeutic area support through engaging with SLs/KDMs, driving scientific initiatives and supporting the field force.</li><li>Collect, analyze, and communicate actionable insights at the country level.</li><li>Provide scientific inputs for digital initiatives.</li><li>Successfully collaborate, provide scientific inputs, and lead resolution of Regulatory queries/issues.</li><li>Support execution of and quickly adapt tactical plans to business realities in country.</li><li>Act with ethics and integrity; Provide non-promotional, balanced, reliable and scientific information.</li><li>Support with therapy training content for Sales team.</li><li>Demonstrate strategic thinking, specifically related to asset value proposition, and clinical and value evidence.</li><li>Support creation of Medical Affairs Plans along with the TA and META cluster Medical Leads.</li></ul><p></p><p>
Medical Information</p><p></p><ul><li>Provide prompt medical information support, such as research and answering of medical inquiries from external and internal customers.</li></ul><p></p><p><b>
Required Education, Experience and Skills</b></p><p><br>
</p><ul><li>Minimum of 4 year's experience in filed medical affairs.</li><li>
Pharma industry experience required, minimum 5 years in multinational company.</li><li>
Medical degree, PhD, Pharm D or other relevant life sciences degree.</li><li>
Ability to communicate knowledge of the therapeutic area, through scientific exchange in different environments and with different stakeholders (one on one, lectures, etc.)</li><li>
Ability of critical lecture of the medical literature related to the therapeutic area</li><li>
Ability to analyze medical literature in order to evaluate the different tendencies in research</li><li>
Strong scientific baseline knowledge in assigned therapeutic area(s).</li><li>
Scientific leadership</li><li>
Ability to communicate knowledge of the therapeutic area, through scientific exchange in different environments and with different stakeholders (one on one, lectures, etc)</li><li>
Ability of critical lecture of the medical literature related to the therapeutic area</li><li>
Demonstrate strategic thinking, specifically related to asset value proposition, and clinical and value evidence</li><li>
Strategic planning</li><li>
High level of scientific and ethical integrity.</li><li>
Excellent communication skills, including listening and probing skills, across a variety of internal and external audiences.</li><li>
Strong collaboration and negotiation skills and ability to function within a team environment.</li><li>
Problem solving</li><li>
Analytical skills</li><li>
Understanding of core systems, tools and metrics related to medical literature</li><li>
Excellent written and oral proficiency in English</li><li>
Complex projects management</li><li>
Candidate must be based in Cairo</li></ul><p></p><p><b>
Secondary Job Description</b></p><p></p><p><b>
Who We Are:
</b></p><p>Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women&rsquo;s Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman.</p><p></p><p>
As an equal opportunity employer, we welcome applications from candidates with a diverse background. We are committed to creating an inclusive environment for all our applicants.</p><p></p><p><b>
Search Firm Representatives Please Read Carefully</b><br>
Organon LLC, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.</p><p></p><p><b>
Annualized Salary Range</b></p><p></p><p><b>
Annualized Salary Range (Global)</b></p><p><b>
Annualized Salary Range (Canada)</b></p><p><b>
Please Note: Pay ranges are specific to local market and therefore vary from country to country.</b></p><p></p><p><b>
Employee Status:
</b></p>Regular<p></p><p><b>
Relocation:</b></p>
No relocation<p></p><p><b>
VISA Sponsorship:</b></p><p></p><p><b>
Travel Requirements: Organon employees must be able to satisfy all applicable travel and credentialing requirements, including associated vaccination prerequisites</b></p><p></p><p><b>
Flexible Work Arrangements:</b></p><p></p><p><b>
Shift:</b></p><p></p><p><b>
Valid Driving License:</b></p><p></p><p><b>
Hazardous Material(s):</b></p><p></p><p><b>
Number of Openings:
</b></p>1<p><b><br>
Requisition ID:</b>R539260</p></div>

Associate Director, Medical Affairs - Egypt

<div>
 <p>
  The Client Affairs Director is responsible for leading and managing all client-facing operations across the post-sales customer journey, including property handover, customer service operations, and call center management. This role ensures a seamless and positive customer experience from unit readiness through handover and ongoing client support.
 </p>
 <p>
  <br/>
 </p>
 <p>
  The Client Affairs Director plays a critical role in strengthening customer trust, enhancing brand reputation, and ensuring the successful delivery of projects from a client experience perspective. Real estate development experience is essential, while community management exposure is considered a strong advantage.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Job Responsibilities:
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Lead and manage the Client Affairs function, overseeing customer service, call center operations, and property handover activities to ensure a consistent and high-quality client experience.
  </li>
  <li>
   Develop and implement client service strategies, policies, and procedures to enhance customer satisfaction and strengthen long-term relationships with clients.
  </li>
  <li>
   Oversee the end-to-end handover process, ensuring proper coordination with Development, Construction, Finance, and Legal teams to deliver units to clients smoothly and in line with company standards.
  </li>
  <li>
   Ensure efficient management of customer inquiries, requests, complaints, and escalations across all service channels including call center, digital platforms, and customer service offices.
  </li>
  <li>
   Establish and monitor service level agreements (SLAs), quality standards, and operational procedures to maintain high performance in customer service and call center operations.
  </li>
  <li>
   Monitor client feedback, satisfaction surveys, and service performance data to identify improvement opportunities and enhance overall client experience.
  </li>
  <li>
   Coordinate with internal departments to resolve technical, contractual, or financial client issues and ensure timely resolution of client concerns.
  </li>
  <li>
   Develop reporting dashboards and performance metrics related to handover operations, customer satisfaction, service response times, and complaint resolution.
  </li>
  <li>
   Lead, mentor, and develop the Client Affairs team to ensure high performance, service excellence, and alignment with the company&rsquo;s customer experience strategy.
  </li>
  <li>
   Support the transition of clients from handover to community management or property management teams to ensure continuity of service and resident satisfaction.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  Job Requirements:
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   - Education:
  </strong>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Business Administration, Marketing, Management, or a related field.
  </li>
  <li>
   Professional certifications in Customer Experience or Service Management are considered an advantage.
  </li>
 </ul>
 <p>
  <strong>
   - Previous Experience:
  </strong>
 </p>
 <ul>
  <li>
   Minimum 5 years in a leadership role in customer service, client relations, or customer experience within the real estate development sector.
  </li>
  <li>
   Proven experience managing property handover operations, customer service teams, and call center functions in real estate developers.
  </li>
 </ul>
 <p>
  <strong>
   - Special requirements:
  </strong>
 </p>
 <ul>
  <li>
   Community management or property management exposure is a plus.
  </li>
  <li>
   Strong knowledge of the real estate customer lifecycle including sales support, unit handover, and post-handover service.
  </li>
  <li>
   Strong problem-solving and conflict resolution capabilities with a customer-centric mindset.
  </li>
  <li>
   Ability to analyze customer feedback and operational data to drive service improvements.
  </li>
 </ul>
</div>


Client Affairs Director

Glenmark Pharmaceuticals

<div>
 <p>
  <strong>
   <u>
    Role Overview:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  The Medical Science Liaison (MSL) &ndash; Oncology is a field-based medical professional responsible for executing Glenmark&rsquo;s medical affairs strategy in the region assigned for oncology products across their lifecycle, including pipeline and marketed assets.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Working in close alignment with Global Medical Affairs and the local cross-functional team, the MSL serves as a scientific expert and trusted partner to oncologists, hematologists, investigators, and other key healthcare stakeholders. The role focuses on high-quality, non-promotional scientific exchange, medical insight generation, and support of evidence generation initiatives, while ensuring full compliance with local regulations, including local regulatory requirements and the Code of Conduct
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Job Responsibilities:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Identifies, maps, and develops scientific relationships with key oncology KOLs, investigators, and cancer centers across regions assigned in alignment with the medical strategy.
  </li>
  <li>
   Conducts high-quality, non-promotional scientific exchange with HCPs, ensuring fair-balanced communication of clinical data, benefits, risks, and appropriate use of Glenmark oncology products.
  </li>
  <li>
   Gathers, analyses, and communicates actionable medical insights from the field to inform local and global medical strategies.
  </li>
  <li>
   Supports planning and execution of medical education initiatives such as advisory boards, medical education programs (MEPs), and focused group discussions.
  </li>
  <li>
   Supports clinical evidence generation activities including investigator-initiated studies, real-world evidence initiatives, and company-sponsored studies in collaboration with Global Medical and Clinical teams.
  </li>
  <li>
   Maintains in-depth knowledge of disease areas, treatment paradigms, competitive landscape, and local treatment guidelines relevant to assigned oncology assets
  </li>
  <li>
   Provides scientific training and medical input to internal stakeholders, including sales and cross-functional teams, ensuring accuracy and compliance.
  </li>
  <li>
   Attends local and regional oncology congresses and scientific meetings to remain current on emerging data and evolving standards of care.
  </li>
  <li>
   Responds to unsolicited medical information requests in a timely, accurate, and compliant manner, in collaboration with Medical Information and PV teams.
  </li>
  <li>
   Ensures all medical activities are conducted in compliance with Glenmark SOPs, health authority regulations, and the local code of conduct
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Educational Qualifications:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Advanced degree in Life Sciences or Healthcare (PharmD, M. Pharm, PhD, Msc, MBBS, BDS or equivalent)
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   <u>
    Experience:
   </u>
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  Minimum 2&ndash;4 years of experience as a Medical Science Liaison, preferably in Oncology. Experience engaging with oncology stakeholders within the country healthcare system is strongly preferred. Familiarity with local regulatory requirements, clinical research processes, and medical affairs operations
 </p>
</div>


Medical Science Liaison

Holcim

<div></div><div><div><div><div><div><p>Export Lead
</p></div></div></div></div><div><div><div><div><b>Location:
</b>New Cairo, Cairo, EG, 11835
</div></div></div></div><div><div><div><div><b>Requisition ID: </b>15010
</div></div></div></div><div></div><div><div><p><b>Why work for us?</b><br>
Driven by our purpose: Building progress for people and the planet. We are transforming to become the leader in innovative and sustainable building solutions. Holcim US offers an unparalleled range of innovative cement, aggregates, asphalt, concrete products and construction services that have been the foundation for infrastructure projects across the globe. To move the industry forward to a greener future we need people who are passionate about sustainability, are driven to shape and influence perception, and keen to build, grow and thrive in our high-performance culture. <b>Are you ready to build progress with us?</b></p>
</div></div><div><div><div><div><div><div><div><div><div><b>Export Lead</b></div></div></div><div><br>
<div>
<div><b>Job Purpose</b><br>
<br>
</div></div><div></div><div><ul><li>Responsible for handling clinker and cement export sales, ensuring seamless communication, coordination, and follow-up with internal and external stakeholders (production, packing, sales, finance, logistics, procurement, RT safety, transporters, ports, stevedores, and governmental authorities). The role focuses on maximizing profitability, ensuring customer satisfaction, achieving export objectives, and maintaining compliance with country and RT safety standards.</li></ul></div><br>
</div><br>
<div><div><div><b>Key Responsibilities</b></div></div><div></div><div><br>
<div><b>
 Health &amp; Safety:</b></div>
<ul>
<li>Adhere to and enforce relevant legislations and policies.</li>
<li>Ensure that highest degree of safety and safe working practices are maintained.</li></ul><br>
<div></div>
<div><b>
Functional:</b></div><br>
<div></div>
<div><b>
Business Development &amp; Customer Management</b></div><br>
<div></div>
<ul>
<li>Acquire new export business leads and manage customer accounts.</li>
<li>Maintain strong relationships with existing customers, including order processing, payment registration, financial guarantees, and addressing requirements through coordination with internal teams (production, finance, etc.).</li>
<li>Identify customer needs and support product/price development by monitoring industry trends and competitor activities.</li>
<li>Explore and pursue new business opportunities by approaching prospects and assessing their market position.</li>
<li>Present and demonstrate products and services to customers.</li></ul><br>
<div></div>
<div><b>
Sales Strategy &amp; Performance Monitoring</b></div><br>
<div></div>
<ul>
<li>Formulate and implement export sales strategies to ensure target achievement for each customer.</li>
<li>Monitor and follow up on customer performance to ensure compliance with agreed targets.</li>
<li>Prepare and update daily, weekly, and monthly reports (projections, forecasts, export dispatches, sales, and revenue).</li>
<li>Monitor export movements to develop market intelligence.</li></ul><br>
<div></div>
<div><b>
Operations &amp; Logistics Coordination</b></div><br>
<div></div>
<ul>
<li>Follow up on the execution of export operations by coordinating with stakeholders (maritime agents, stevedoring companies, inspection firms, vessel crews, port authorities, production, packing, finance, logistics, procurement, RT safety, LH trading).</li>
<li>Oversee export business activities at warehouses and ports (Adabeya, Damietta, Dekheila, Alexandria, Sokhna).</li>
<li>Coordinate with stevedoring companies to achieve agreed vessel loading rates.</li>
<li>Follow up on stevedore payments and manage debit/credit notes to settle demurrage/dispatch issues.</li>
<li>Monitor cement and bag stock levels to ensure product availability and coordinate with plant operations for material creation.</li></ul><br>
<div></div>
<div><b>
Compliance &amp; Documentation</b></div><br>
<div></div>
<ul>
<li>Handle all commercial documentation (customer and material creation, offers in SFDC, invoicing, banking, and customs clearance).</li>
<li>Liaise with governmental authorities (Customs, Chambers of Commerce, Export &amp; Import Control, and Port Authorities) to fulfill regulatory requirements and new decrees.</li>
<li>Review and validate Form 13 submissions from business partners and coordinate with the Tax department.</li>
</ul><ul><li>Handle treasury procedures to secure CBE approvals and required delegations for export activities.</li>
<li>Archive all shipment documents and ensure reporting accuracy.</li></ul></div></div><div><br>
<div>
<div></div><div><b>Education</b></div><br>
<div></div>
<div><b>
Qualifications &amp; Experience</b></div></div><div><div><br>
</div> <div><b>Education:</b></div><br>
<div></div>
<ul>
<li>Bachelor degree in Business Administration, International Trade, Logistics, or a related field.</li></ul><br>
<div></div>
<div>
 <b>Experience:</b></div>
<ul>
<li>Minimum of 6&ndash;7 years of experience in export sales, logistics, or international trade, preferably within the cement, building materials, or industrial sector.</li>
</ul>
</div></div><br>
</div></div></div></div></div></div><div><div><p><b>WHO ARE LAFARGE PEOPLE?</b><br>
Lafarge people are passionate about finding better ways to build. They embrace innovation and improvement with a pioneering spirit. They work as trusted partners, creating better solutions and experiences for their customers, communities, and colleagues.</p>
<p><b>YOUR LAFARGE EXPERIENCE</b><br>
At Lafarge, there is endless opportunity for you to play your part. Whether you&rsquo;re in a technical, managerial, or frontline role, you can shape a career that works for you. With us you&rsquo;ll have the chance to embrace the passion we share for our planet. You&rsquo;ll be encouraged to seek out diverse perspectives, share your ideas, and build the skills and connections you need to perform at your best. Because it&rsquo;s only when we work together in a culture where everyone thrives, that we can build the world we all want to live in.</p></div></div></div><p></p>

Export Lead

Amgen

<div><p><b>HOW MIGHT YOU DEFY IMAGINATION? </b>If you feel like you&rsquo;re part of something bigger, it&rsquo;s because you are. At Amgen, our shared mission&mdash;to serve patients&mdash;drives all that we do. It is key to our becoming one of the world&rsquo;s leading biotechnology companies. We are global collaborators who achieve together&mdash;researching, manufacturing, and delivering ever-better products that reach over 10 million patients worldwide. It&rsquo;s time for a career you can be proud of. Join us.</p><p></p><p>
Regulatory Affairs &quot;Labelling&quot; Manager| MEA</p><p></p><p><b>
Scope:
</b></p><p></p><p>Accountable for end‑to‑end execution of compliant, accurate, and timely local product labeling and packaging deliverables across assigned MEA markets. Ensures alignment with Global Core Labeling (GCL) and company labeling governance while incorporating local Health Authority requirements, language conventions, and lifecycle changes.</p><p></p><p><b>
Key Responsibilities:</b></p><ul><li>
Own and execute local labeling activities for assigned products/country clusters (e.g., SmPC/PI, PIL/leaflet, carton/label text, IFU), ensuring content accuracy, completeness, and compliance.</li><li>
Translate global core updates into local implementation plans: perform impact assessments, draft/redline local texts, coordinate review/approval, and support submission strategy for labeling variations/line extensions.</li><li>
Act as local/regional **source text owner** for artwork creation: deliver &lsquo;right‑first‑time&rsquo; source texts and maintain traceability from CDS/CCDS/GCL changes to country label implementation.</li><li>
Coordinate packaging and artwork lifecycle activities (leaflet, label, blister, outer pack): initiate and manage updates, support shared pack/SKU strategy execution, and ensure supply‑readiness timelines are met.</li><li>
Manage translation workflows (including engaging translation agency systems): request translations, track readiness, and perform **100% translation review** for both content and format (as required for regional languages).</li><li>
Execute labeling/artwork review and approval tasks in designated systems (e.g., Veeva Vault, RIM/Regulatory Information Management, artwork management tools), maintaining version control and inspection‑ready documentation.</li><li>
Monitor and report operational metrics (e.g., right‑first‑time labels, cycle time, on‑time delivery) and drive corrective actions for recurring defects or bottlenecks.</li><li>
Support biosimilars labeling redaction/maintenance activities (as applicable to assigned portfolio).</li><li>
Support track‑and‑trace/serialization intelligence gathering and execution for assigned clusters; ensure packaging/labeling requirements are reflected in artworks and implementation plans.</li><li>
Draft, update, and/or support local SOPs and work instructions related to labeling management; ensure adherence to internal procedures and quality standards.</li><li>
Identify labeling and packaging risks (compliance, timelines, translations, artwork quality) and proactively propose mitigations; escalate issues per governance.</li></ul><p></p><p><b>
Qualifications:</b></p><ul><li>
Bachelor&rsquo;s degree in Pharmacy or related life sciences (required); advanced degree is an advantage.</li><li>
Typically 4&ndash;8+ years of Regulatory Affairs experience with strong hands‑on labeling and artwork/packaging lifecycle management.</li><li>
Current or previous experience within MNCs is a must.</li><li>
Knowledge of Middle East &amp; Africa regulatory requirements and practical experience coordinating multi‑country implementations.</li><li>
Language skills: English (required); French literacy strongly preferred; Arabic preferred when the role includes Arabic translation review responsibilities.</li><li>
Demonstrated proficiency working in regulated document and workflow systems (e.g., Veeva Vault, RIM tools) and in cross‑functional matrix environments.</li><li>
Skills/behaviors: detail orientation, planning/priority management, proactive risk management, clear written/oral communication, cultural awareness, and a quality mindset.</li></ul><p></p><p><b>
Thrive What You Can Expect Of Us </b>As we work to develop treatments that take care of others, so we work to care for our teammates&rsquo; professional and personal growth and well-being.</p><br>
<ul><li>
Vast opportunities to learn and move up and across our global organization</li><li>
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act</li><li>
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits</li></ul><p><b>
Apply now for a career that defies imagination </b>In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.<br>
<br>
<b>careers.amgen.com </b>Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, gender, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p></div>

Regulatory Affairs "Labelling" Manager| MEA

Explore 182+ Governmental affairs specialist in Egypt this April. Find roles across top companies and apply now to boost your career.

182 governmental affairs specialist jobs In Egypt

Governmental Affairs Specialist

Governmental Affairs Specialist

Associate Director, Medical Affairs - Egypt

Client Affairs Director

Medical Science Liaison

Export Lead

Regulatory Affairs "Labelling" Manager| MEA