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corporate affairs manager

Giza Systems

<div>
 
 
 Job Description
 
 
 
 The Corporate Affairs Manager serves as a strategic legal advisor across Giza Systems functions, providing expert counsel on corporate governance, compliance, and regulatory matters. This role supports key initiatives such as M&amp;A transactions, risk management, and corporate strategy, while ensuring adherence to governance frameworks and legal obligations.
 
 
 
 Responsibilities
 
 include overseeing board and committee processes, preparing and maintaining critical documentation, and collaborating with stakeholders to mitigate legal risks through robust controls and procedures.
 
 
 Acting as a trusted partner to executive management, the Corporate Affairs Manager delivers actionable insights and guidance to safeguard the organisation&rsquo;s interests and enable informed decision-making.
 
 
 
 Legal Advisory &amp; Risk Management
 
 
 <ul>
 <li>
 Provide legal advice, guidance, and recommendations across GS functions based on thorough research and analysis.
 </li>
 <li>
 Support corporate strategy &amp; planning with legal counsel on potential M&amp;A transactions.
 </li>
 <li>
 Advise the Governance, Risk, and Compliance (GRC) team on applicable laws, regulations, and compliance obligations.
 </li>
 <li>
 Monitor business operations to identify legal risks and collaborate on mitigation strategies, including controls, insurance, and documentation.
 </li>
 <li>
 Respond to executive management enquiries on strategic legal matters, offering insights and risk assessments.
 </li>
 </ul>
 
 
 Corporate Governance &amp; Compliance
 
 
 <ul>
 <li>
 Oversee and manage all legal processes related to corporate governance and compliance.
 </li>
 <li>
 Ensure adherence to governance frameworks and regulatory requirements.
 </li>
 <li>
 Prepare and review agendas, resolutions, and minutes for Board, OGA, and EOGA meetings.
 </li>
 <li>
 Coordinate logistics and documentation for board and committee meetings.
 </li>
 <li>
 Manage archiving of all related documentation in coordination with the Contracts team, ensuring proper accessibility.
 </li>
 </ul>
 
 
 Personal Skills
 
 
 <ul>
 <li>
 Strong Communication &amp; Negotiation
 </li>
 <li>
 Exceptional analytical and problem-solving abilities
 </li>
 <li>
 Strong leadership and team management skills
 </li>
 <li>
 Excellent communication and negotiation skills
 </li>
 </ul>
 
 
 Technical Skills
 
 
 <ul>
 <li>
 Bachelor of Law with experience from 12 to 15 years
 </li>
 <li>
 Corporate Law &amp; Governance
 </li>
 <li>
 Regulatory Compliance &amp; GRC Advisory
 </li>
 <li>
 Mergers &amp; Acquisitions (M&amp;A) Legal Support
 </li>
 <li>
 Legal Risk Assessment &amp; Mitigation
 </li>
 <li>
 Executive-Level Legal Counsel
 </li>
 <li>
 Cross-Functional Collaboration (Strategy, GRC, Operations)
 </li>
 <li>
 Business Risk Analysis &amp; Operational Controls
 </li>
 </ul>
</div>

Corporate Affairs Manager

MAGRABi Retail Group

<div>
 
 
 JOB PURPOSE
 
 
 
 
 
 
 The Lead &ndash; Legal Affairs &amp; Compliance provides advanced legal support across all MAGRABi entities within the region. The role ensures effective legal risk management, delivers high-quality legal advice to business units, and supports the implementation of standardized legal processes, templates, and governance frameworks. This position plays a central role in contract negotiation, corporate documentation, and the development of a unified regional legal function.
 
 
 
 
 
 Qualifications and Education:
 
 
 
 
 
 &bull; Bachelor&rsquo;s degree in law from a recognized university.
 
 
 &bull; Master&rsquo;s degree in law or relevant certification (preferred).
 
 
 &bull; Admitted to the bar in Egypt.
 
 
 &bull; Excellent legal drafting, negotiation, and analytical skills.
 
 
 &bull; Strong understanding of corporate governance and regulatory requirements.
 
 
 &bull; Familiarity with legal archiving systems and contract management processes.
 
 
 &bull; Proficiency in MS Office; exposure to legal automation tools is an advantage.
 
 
 &bull; Fluent in Arabic and English (written and spoken).
 
 
 
 
 
 Experience:
 
 
 
 
 
 &bull; 7-9 years of post-qualification legal experience.
 
 
 &bull; Strong background in corporate, commercial, and contracts law.
 
 
 &bull; M&amp;A experience is a plus.
 
 
 &bull; Experience supporting multinational or multi-country operations.
 
 
 &bull; Proven experience handling external counsel and litigation coordination.
 
 
 &bull; Experience in corporate governance, statutory compliance, and regulatory dealings.
 
 
 
 
 
 
 JOB RESPONSIBILITIES
 
 
 
 
 
 
 &bull; Draft, review, and negotiate complex and high-value contracts to protect the company&rsquo;s commercial and legal interests.
 
 
 &bull; Prepare and manage corporate documentation, including PoAs, shareholder records, board resolutions, and filings, to ensure compliance with governance standards.
 
 
 &bull; Provide comprehensive legal advice to business units on corporate, commercial, and operational matters to minimize risk and support informed decisions.
 
 
 &bull; Support litigation and dispute resolution, coordinating with external counsel to ensure efficient case management.
 
 
 &bull; Develop and maintain standard legal templates, policies, and workflows to enhance consistency across the region.
 
 
 &bull; Mentor the Executive &ndash; Legal Affairs &amp; Compliance, ensuring effective task execution, proper
 
 
 documentation, and structured archiving.
 
 
 &bull; Support M&amp;A and restructuring matters, including due diligence, regulatory filings, and integration processes.
 
 
 &bull; Prepare regular legal, compliance, and risk reports for the Senior Legal Manager to assist in strategic decision-making.
 
 
 &bull; Support regional legal matters as assigned to ensure alignment across all MAGRABi countries and contribute to the unified regional legal function.
 
</div>

Lead - Legal Affairs & Compliance

PepsiCo

<div>
 
 Overview
 
 
 
 This role is responsible for supporting EMEA Procurement Control in financial reporting and analytics through accurate data collection, in-depth analysis, precise reporting, and process improvement initiatives. It requires strong analytical skills and excellent organizational abilities to manage complex datasets, coordinate across multiple stakeholders, and ensure timely issue resolution.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Preparing EMEA Procurement Cash Flow productivity reporting - data collection from the contracts management system and from whole legacy Europe Procurement community (ca 500 associates) as well as the legacy AMESA point of contacts; review the accuracy of provided information, perform data analysis and identification of key variance drivers; managing calculation of Cash Flow; results reporting to EMEA Business Unit Controllers and to Corporate FP&amp;A team.
 </li>
 <li>
 Mark to Market reporting from Derivatives and Forex Embedded Derivatives in legacy Europe Procurement managed contracts - data collection from contracts management tool; data analysis for the existence of derivatives/ Forex embedded derivatives: collecting information for the correct Mark to Market calculations per contract (information related to contracts from Procurement Managers, Executed Hedges, Forex Forward rates from Corporate Treasury). Data reporting to Corporate Embedded Derivatives Centre of Excellence and to EMEA Sector Control.
 </li>
 <li>
 Extended Producer Responsibility reporting for Europe - data collection from Business Units; results verification and reporting to Corporate Government Affairs.
 </li>
 <li>
 Acting as a SPOC for Benelux Accounts Payable - resolving issues with blocked POs which can cause payment delays to our suppliers; analyzing weekly report received from Benelux AP team; connecting with employees and guide on actions required for resolving issues.
 </li>
 <li>
 Supporting ad-hoc projects and process improvements initiatives assigned by Europe Procurement Control and issue resolution for the mentioned scope.
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Bachelor in Economics or Finance with main focus on Finance/Control &amp; Accounting or at least 3-4 years experience in Finance/Control &amp; Accounting, ideally in a global FMCG company
 </li>
 <li>
 Excellent English language skills (read, write, speak)
 </li>
 <li>
 Strong analytical skills
 </li>
 <li>
 Good accounting / internal controls knowledge
 </li>
 <li>
 Very good Excel knowledge
 </li>
 <li>
 Ability to work across various countries and cultures
 </li>
 </ul>
</div>

Control & Reporting Asst Analyst

WhiteCrow Research

<div>
 
 
 About WhiteCrow
 
 
 
 
 
 
 We are global talent research, insight, and sourcing specialists with offices in the UK, USA, Singapore, Malaysia, Hong Kong, Dubai, and India. Our international reach has helped us to understand and penetrate specialist markets at a global level. In addition to this, our service is also extended to complement our client&rsquo;s in-house talent acquisition teams.
 
 
 
 
 
 
 About our client
 
 
 
 
 
 
 Our client vision is to be the world&rsquo;s best performing snacks-led powerhouse, unleashing the full potential of their differentiated brands.
 
 
 
 
 
 Powered by their strategy to Differentiate, Drive &amp; Deliver, they are a leading company in global snacking, international cereal and noodles, and North America frozen foods, with iconic, world-class brands and strong underlying growth momentum and profitability.
 
 
 Our client purpose is to create better days and a place at the table for everyone through their trusted foods brands.
 
 
 
 
 
 As part of this purpose, they are committed to advancing sustainable &amp; equitable access to food by creating Better Days for 4 billion people by the end of 2030.
 
 
 
 
 
 
 About the role
 
 
 
 
 
 <ul>
 <li>
 We are seeking a qualified and experienced Corporate Legal Counsel to join our Legal team in Egypt.
 </li>
 <li>
 This middle management role supports corporate legal operations across Egypt and support MENAT region, with a focus on contract management, governance, regulatory compliance, and internal advisory.
 </li>
 <li>
 The successful candidate will report directly to the Head of Legal and act as a legal business partner to internal stakeholders.
 </li>
 </ul>
 
 
 
 
 
 As a Corporate Legal Counsel, you will be responsible for...
 
 
 
 
 
 
 
 
 Corporate and Regional Support
 
 
 
 <ul>
 <li>
 Assisting in reviewing corporate processes and documentation within Egypt.
 </li>
 <li>
 Supporting legal coordination and compliance efforts across the MENAT region.
 </li>
 <li>
 Maintaining and updating corporate records and filings in accordance with internal and regulatory requirements.
 </li>
 <li>
 Supporting corporate secretarial functions across the region and ensure timely documentation.
 </li>
 </ul>
 
 
 
 
 
 
 Contract Management and Documentation
 
 
 
 <ul>
 <li>
 Drafting, reviewing, and revising legal documents including but not limited to contracts, NDAs, service agreements, B2B/B2C agreements, and purchase orders.
 </li>
 <li>
 Collaborating with internal teams and external counsel to ensure contractual terms meet legal and business objectives.
 </li>
 <li>
 Maintaining organized records of executed agreements and develop standardized templates.
 </li>
 </ul>
 
 
 
 
 
 
 Governance and Compliance
 
 
 
 <ul>
 <li>
 Assisting in implementing internal governance policies and monitor compliance.
 </li>
 <li>
 Conducting legal research and support risk assessments related to business decisions.
 </li>
 <li>
 Identifying potential legal risks and escalate issues to the Head of Legal with recommended solutions.
 </li>
 </ul>
 
 
 
 
 
 
 Legal Advisory and Communication
 
 
 
 <ul>
 <li>
 Providing clear explanations of legal terms and obligations to internal stakeholders.
 </li>
 <li>
 Providing legal opinion and consultations to internal stakeholders.
 </li>
 <li>
 Acting as a liaison between the legal department and other business units.
 </li>
 <li>
 Preparing legal summaries and reports for senior legal review.
 </li>
 </ul>
 
 
 
 
 
 
 Regulatory and Governmental Affairs
 
 
 
 <ul>
 <li>
 Supporting corporate matters including GAFI documentation and authentication processes.
 </li>
 <li>
 Liaising with governmental authorities regarding licensing and regulatory compliance.
 </li>
 <li>
 Ensuring adherence to company HSE policies and contribute to legal compliance in risk assessments.
 </li>
 <li>
 Handling external law firms and corporate secretariate work and have the ability to draft bilingual OGMs, EGMs and BoDs.
 </li>
 </ul>
 
 
 
 
 
 What you already have...
 
 
 
 
 
 <ul>
 <li>
 Bachelor of Law (LL.B.) or Juris Doctor (J.D.) with a minimum grade of &ldquo;Good&rdquo;.
 </li>
 <li>
 Master of Laws (LL.M) or equivalent postgraduate qualification is a plus.
 </li>
 <li>
 4 &ndash; 7 years of experience in corporate law within a reputable law firm or multinational organization.
 </li>
 <li>
 Admitted to the Egyptian Bar Association.
 </li>
 <li>
 Fluent in English and Arabic (written and spoken).
 </li>
 <li>
 Strong knowledge of contract law, corporate governance, licensing, and regulatory frameworks.
 </li>
 <li>
 Familiarity with GAFI procedures and governmental dealings.
 </li>
 <li>
 Litigation experience is a plus.
 </li>
 </ul>
</div>

Corporate Legal Counsel

Johnson & Johnson Innovative Medicine

<div>
 At Johnson &amp; Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com
 
 
 
 Job Function
 
 
 
 Medical Affairs Group
 
 
 
 Job Sub Function
 
 
 
 Medical Science Liaison
 
 
 
 Job Category
 
 
 
 Scientific/Technology
 
 
 
 All Job Posting Locations:
 
 
 
 Cairo, Egypt
 
 
 
 Job Description
 
 
 
 
 About Immunology
 
 
 
 Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.
 
 
 Our Immunology team leads in the development of transformational medicines for immunological disorders and illnesses. You can influence where medicine is going by restoring health to millions of people living with immune diseases.
 
 
 Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
 
 
 Learn more at https://www.jnj.com/innovative-medicine
 
 
 
 We are searching for the best talent Medical Science Liaison &ndash; Immunology in Cairo, Egypt.
 
 
 
 
 Summary Of The Job
 
 
 
 To be a therapeutic area scientific expert, responsible for discussing our Therapeutic areas, patients&rsquo; treatment trends and studies in the therapeutic areas in which we are involved, on a peer-to-peer basis with a defined audience of Leading Specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other stakeholders) and to be considered a trusted scientific counterpart and partner.
 
 
 
 Duties &amp; Responsibilities
 
 
 
 <ul>
 <li>
 To keep abreast of medical and scientific knowledge.
 </li>
 <ul>
 <li>
 Continuously update their knowledge of patient&rsquo;s treatment trends, guidelines, clinical activities and studies within the therapeutic area and patient`s treatment trends in the region
 </li>
 <li>
 Identify evolving scientific concepts with future clinical implications.
 
 
 </li>
 </ul>
 </ul>
 <ul>
 <li>
 Development and maintenance of a contact network with Leading Specialists.
 </li>
 <ul>
 <li>
 Understand their needs, key value drivers, practical treatment patterns and scientific activities within the therapeutic area.
 </li>
 <li>
 Develop and execute an external stakeholder management plan in close collaboration and coordination with other functions including HEMAR, Commercial, Global clinical operations, medical information and pharmacovigilance.
 </li>
 <li>
 Through scientific interactions, champion the medical value of our products fairly based on the risk-benefit profile of our drugs and contribute to the fostering of innovative approaches.
 </li>
 <li>
 Represent the company to other therapeutic area stakeholders including professional associations and patient organisations in cooperation with Medical Advisor(s)/Medical Director
 </li>
 <li>
 Recognize and nurture relationships with rising stars within the scientific community.
 
 
 </li>
 </ul>
 </ul>
 <ul>
 <li>
 Proactive and reactive communication of medical scientific data to Leading Specialists and broader external health-care related audiences:
 </li>
 <ul>
 <li>
 Communicate non-promotional general information about our company, including pipeline, research and development programs and other relevant information.
 </li>
 <li>
 Respond to unsolicited scientific queries from customers for approved products and products/indications in development, based on Medical Affairs and Medical Information documents.
 </li>
 <li>
 Use digital technologies and new media to support proactive and reactive communication.
 
 
 </li>
 </ul>
 </ul>
 <ul>
 <li>
 Organization and participation in Medical Education activities:
 </li>
 <ul>
 <li>
 Identify/support/educate speakers.
 </li>
 <li>
 Build Medical Education programs with scientific third parties and scientific steering committees.
 
 
 </li>
 </ul>
 </ul>
 <ul>
 <li>
 Participation in Advisory Boards in cooperation with Medical Lead/Medical director
 </li>
 <li>
 Provision of scientific support to company Sales Representatives
 </li>
 <ul>
 <li>
 Provide medical and product training and scientific support to Sales Representatives in coordination with Training Departments as appropriate.
 </li>
 <li>
 Act as a reference point for sales representatives for any scientific query, in collaboration with Medical Information as appropriate
 
 
 </li>
 </ul>
 </ul>
 <li>
 Support Medical Affairs clinical activities strategy, planning, design and execution in close co-operation with GCO and CROs when applicable.
 </li>
 <ul>
 <li>
 Support the set up and follow up of registries and other non-interventional Medical Affairs studies.
 </li>
 <li>
 Understand Real World Evidence (RWE) methodologies, identify data needs and opportunities, support protocol development and engage in discussions with customers to help design RWE projects.
 </li>
 <li>
 Propose investigators and sites for interventional and non-interventional Medical Affairs studies.
 </li>
 <li>
 Support GCO and CROs in site set up, management and issue resolution.
 </li>
 <li>
 Contribute to preparation and conduct of investigator meetings, recruitment follow-up and study result presentation.
 </li>
 <li>
 Manage investigator proposals for IISs and ensure they are discussed within the Medical Affairs department for decision.
 </li>
 <li>
 Support post marketing surveillance and expanded access programs
 </li>
 <li>
 Manage field based medical projects.
 </li>
 <li>
 Through scientific interactions, gain valuable insights into treatment patterns, and scientific activities in the therapeutic area and provide strategic input to the company Medical Affairs plan/ business decision-making.
 
 
 </li>
 </ul>
 
 Main performance measures (Performance Goals)
 
 
 
 <ul>
 <li>
 80% of time is spent in the field.
 </li>
 <li>
 Ability to shape the treatment algorithm in the respective TA through Medical education/peer to peer interactions.
 </li>
 <li>
 Establishing Janssen as #1 scientific partners to leading specialists
 </li>
 <li>
 Establish the value of Janssen brands among the scientific community
 
 
 </li>
 </ul>
 
 Experience Required
 
 
 
 <ul>
 <li>
 MD/Pharmacist/Physicians/Dentist degree.
 </li>
 <li>
 Minimum 4+ years of experience in a multinational pharmaceutical company.
 </li>
 <li>
 Experience in immunology is preferable.
 </li>
 <li>
 Experience of 1-2 years as an MSL is an advantage, or pharmacist holding master degree/Pharm D.
 
 
 </li>
 </ul>
 
 Leadership Behaviors Required
 
 
 
 <ul>
 <li>
 LIVE OUR CREDO: Puts the needs of Our Credo stakeholders first, pursues the highest standards of quality, safety, compliance &amp; ethics and ensures everyday actions contribute to Our Purpose
 </li>
 <li>
 CONNECT: Builds internal and external relationships based on respect, collaborates openly across boundaries and acts as a team player.
 </li>
 <li>
 SHAPE: Inspires and contributes ideas that challenge thinking, demonstrates resilience and agility to drive and adapt to change.
 </li>
 <li>
 Grow: Develops self and others to reach their goals, engages in open &amp; honest conversations and Drives performance by managing energy and taking ownership for outcomes.
 
 
 </li>
 </ul>
 
 Required Skills
 
 
 
 
 Preferred Skills:
 
</div>

Medical Science Liaison - Immunology

Novo Nordisk

<div>
 Shape how Novo Nordisk Egypt tells its story &mdash; lead integrated communications with a robust focus on media and digital channels (including social media), and sustainability initiatives that strengthen reputation, support business priorities in cardiometabolic and rare diseases, and engage both external stakeholders and our people.
 
 
 
 Your new role
 
 
 
 You will plan, produce and execute integrated communication initiatives across internal and external channels to support corporate and divisional goals.
 
 
 Day to day you will:
 
 
 
 <ul>
 <li>
 Develop and implement proactive media relations and dynamic social media strategies that advance Novo Nordisk Egypt&rsquo;s business objectives, especially supporting the launch of key products (branded and unbranded).
 </li>
 <li>
 Lead digital content and campaign execution across all local social media channels, focusing on driving engagement and building buzz among target audiences.
 </li>
 <li>
 Translate business priorities into integrated communications plans, aligning messages with corporate strategy and local needs.
 </li>
 <li>
 Build and maintain strategic relationships with key media outlets, digital agencies, patient advocacy groups (PAGs), and other external stakeholders.
 </li>
 <li>
 Lead issue and crisis communication planning: prepare issues management plans, reactive statements, messaging platforms and media responses in coordination with Global Media Relations.
 </li>
 <li>
 Design and deliver internal communications to inform and engage employees &mdash; using townhalls, newsletters, SharePoint/Yammer, and other local/global tools to strengthen employer reputation and alignment.
 
 
 
 
 </li>
 </ul>
 
 Your new department
 
 
 
 You will join a collaborative corporate affairs team that partners closely with commercial, medical, HR colleagues. The team&rsquo;s purpose is to protect and enhance Novo Nordisk&rsquo;s reputation, enable business outcomes and foster a culture of engagement and trust.
 
 
 
 Your Skills &amp; Qualifications
 
 
 
 We are looking for someone who can combine strategic thinking with strong execution:
 
 
 
 <ul>
 <li>
 University degree, preferably in Communications, Journalism, Public Relations or a related field.
 </li>
 <li>
 At least 5 years&rsquo; experience in communications within the private sector, ideally in FMCG or related industries.
 </li>
 <li>
 Demonstrated experience in communications planning, media relations, and social media/digital campaign management with a proven track record of successful campaign execution in fast-paced markets.
 </li>
 <li>
 Strong editorial skills and experience producing communication across channels (press, digital campaigns, print, social, audio and video).
 </li>
 <li>
 Proven ability to manage issues and crisis communications, and to prepare clear reactive messaging.
 </li>
 <li>
 Experience in internal communications and employee engagement programs.
 </li>
 <li>
 Experience or strong interest in sustainability communications and stakeholder partnership building.
 </li>
 <li>
 Excellent written and spoken English; Arabic language skills are an advantage.
 </li>
 <li>
 Strong interpersonal skills, stakeholder management and the ability to work cross‑functionally.
 
 
 
 
 </li>
 </ul>
 
 Working at Novo Nordisk
 
 
 
 Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination and a constant curiosity. For over 100 years this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect and a willingness to go beyond what we know delivers extraordinary results.
 
 
 
 What We Offer
 
 
 
 There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.
 
 
 
 Deadline
 
 
 
 25th of December 2025. (Applications are reviewed on an ongoing basis)
 
 
 
 Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.
 
 
 
 We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
 
 
 We&rsquo;re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.
</div>

Communication Manager

Abbott

<div>
 
 Job Title
 
 Regulatory Affairs Manager
 
 
 
 About Abbott
 
 
 
 Abbott is a global healthcare leader, creating breakthrough science to improve people&rsquo;s health. We&rsquo;re always looking towards the future, anticipating changes in medical science and technology.
 
 
 
 Working at Abbott
 
 
 
 At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You will have access to :
 
 
 <ul>
 <li>
 Career development with an international company where you can grow the career you dream of.
 </li>
 <li>
 A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
 </li>
 <li>
 A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
 
 
 </li>
 </ul>
 
 The Opportunity
 
 
 
 This position works out of our [insert location of working site] in the Established Pharmaceutical Division where we are committed to bringing the benefits of our trusted medicines to more people in the world&rsquo;s fastest-growing countries. Our broad portfolio of high-quality and differentiated branded generic medicines reaches across multiple therapeutic areas including gastroenterology, women's health, cardiometabolic, pain management/central nervous system, and respiratory.
 
 
 As the DevOps Director, you&rsquo;ll have the chance to lead a group of engineers to build code for the mobile and Web Cloud platform, working closely with product manager, customer support and testing teams. You&rsquo;ll manage operations, collaborate with security and infrastructure, and support IT defects.
 
 
 
 What You&rsquo;ll Do :
 
 
 
 Core Job Responsibilities :
 
 
 <ul>
 <li>
 Collaborate with Partners to ensure timely and clear dossier requirements are provided to Egypt Affiliate during submission planning
 </li>
 <li>
 Liaise cross-functionally to agree on submission strategy for new products, new indications, renewals and source changes/adds
 </li>
 <li>
 Ensures rapid and timely approval on of new drugs &amp;biologics and continued approved status of marketed products or medical devices.
 </li>
 <li>
 Ensure submission plans are created and maintained in Abbott Regulatory IT tools.
 </li>
 <li>
 Facilitate implementation of the Regulatory Plan in alignment with the business plans.
 </li>
 <li>
 Monitor impact of changing regulations on submission strategies.
 </li>
 <li>
 Negotiate with regulatory authorities during the development and review process to ensure submission approval.
 </li>
 <li>
 Maintain importation plan and align cross functionally on any possible risks.
 </li>
 <li>
 Oversee processes involved with maintaining annual licenses, registrations, listings and patent information.
 </li>
 <li>
 Ensure compliance with product post marketing approval requirements.
 </li>
 <li>
 Review and approve advertising and promotional items to ensure regulatory compliance.
 </li>
 <li>
 Work cross-functionally to obtain all required submission documents and ensure timely responses to Regulatory Authority requests received.
 </li>
 <li>
 Voice Region and Partner perspective and requirements to global regulatory contacts. Coordinate feedback to ensure documents are as required by Partner and use regulatory expertise to provide creative solutions/alternatives in cases where Abbott is unable to meet requirements.
 </li>
 <li>
 Document submission plans and follow-up on progress of submission/timelines with assigned Partner(s) and periodically review with Partner&rsquo;s performance metrics.
 </li>
 <li>
 Serve as affiliate regulatory point person for queries from the business or global functions (GRA, Quality, Supply Chain, Manufacturing) Regulatory Compliance.
 </li>
 <li>
 Ensure data maintenance and data integrity of internal Regulatory IT tools with defined compliance metrics.
 </li>
 <li>
 Ensure implementation of local quality system in line with the global quality system and local regulations.
 </li>
 <li>
 Support internal and external audits / assessments / self-inspections in collaboration with Quality personnel.
 </li>
 <li>
 Implement corrective/preventive actions as appropriate.
 </li>
 <li>
 Raise awareness to relevant functions on compliance issues and initiatives.
 </li>
 <li>
 Ensure timely creation of labelling projects in Agile and liaise with Medical, commercial, quality, Supply Chain and Opx to ensure new/revised labelling available in line with the business plan. Manage submissions and approvals for all labelling updates.
 </li>
 <li>
 Ensure alignment and implementation of internal regulatory initiatives.
 </li>
 <li>
 Identify and present option for risk mitigation to decision makers.
 </li>
 <li>
 Responsible for LOT Release and Submitting the withdrawn product dossiers in NODCAR for analysis.
 
 
 </li>
 </ul>
 
 Required Qualifications
 
 
 
 <ul>
 <li>
 Bachelor's degree of pharmaceutical sciences .
 </li>
 <li>
 At least 7 years industry related experience in Regulatory Affairs.
 
 
 </li>
 </ul>
 
 Preferred Qualifications
 
 
 
 <ul>
 <li>
 Team working skills with special focus on results.
 </li>
 <li>
 Ability to adapt to challenging situations.
 </li>
 <li>
 Biological / Biosimilar registration experience.
 </li>
 <li>
 Demonstrated good computer/IT skills.
 </li>
 <li>
 Good knowledge of written and spoken English &amp; Arabic.
 
 
 </li>
 </ul>
 Other Information/Additional Preferences :
 
 
 <ul>
 <li>
 Analytical, problem solving and negotiation skills.
 </li>
 <li>
 Good communication skills.
 </li>
 <li>
 Project management skills.
 </li>
 <li>
 Strong planning and priority setting.
 </li>
 <li>
 Dynamic and flexible.
 </li>
 <li>
 Problem solver.
 </li>
 <li>
 Good capability to establish positive networking both internally.
 </li>
 <li>
 Strong knowledge of quality systems.
 </li>
 <li>
 Trained on Abbott Regulatory IT tools.
 
 
 </li>
 </ul>
 
 Apply Now
 
 
 
 Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
 
 
 Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
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Regulatory Affairs Manager

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