regulatory affairs sr. manager

senior legal manager

tax & finance compliance manager Jobs in Cairo

tax & finance compliance manager

acquiring business e-commerce relationship manager / senior relationship manager Jobs in Cairo

assistant manager sales operations Jobs in Cairo

assistant manager sales operations

regulatory affairs sr manager

Grifols Egypt for Plasma Derivatives (GEPD)

<div>
 
 Job Objective:
 
 
 
 Regulatory Affairs Senior Manager is the responsible for any communication and coordination with EDA , European Medicines Agency (EMA) and/or other International Health Authorities (as required).
 
 
 Liaison and support between regulatory bodies and operating divisions of the company. Responsible for reviewing and managing the regulatory function by ensuring compliance with (EDA), European Medicines Agency (EMA) and other International Health Authorities (as required), regulations and guidelines to obtain and maintain the corresponding approvals for any GMP area, including Plasma Supply Chain, Manufacturing facility, Exportation / Importation for plasma and/or Final Product in Egyptian Market or others (as required).
 
 
 
 Key responsibility:
 
 
 
 <ul>
 <li>
 Communication with local and international Health Authorities. Support, communication and coordination (as necessary) with local Health Authorities for Plasma Supply chain and Manufacturing facilities for the process of licensing, certification, exportation, importation, and finished product release.
 </li>
 <li>
 Ensure that applicable Health Authorities guidelines, rules and regulations are applied up to date, covering plasma or finished products or GMP sites and regulatory processes.
 </li>
 <li>
 Review and manage the licensing and GMP certification regulatory process for Plasma supply chain and manufacturing. Ensure any submissions related to local and international Health Authority are performed on time for initial licensing and renewal (if applicable) to maintain valid license and/ or certification is maintained in all facilities per existing regulations.
 </li>
 <li>
 Review all the documentations prepared to be submitted to EDA , International Health Authorities and any Certification entities.
 </li>
 <li>
 Change notification to Local and International Health Authorities.
 </li>
 <li>
 Change notification and customers related to Change Control implementation.
 </li>
 <li>
 To assist Direct Manager in any assigned duties.
 </li>
 <li>
 Manage Regulatory Affairs Area to ensure compliance with the above-mentioned points.
 
 
 
 </li>
 </ul>
 
 Academic &amp; Professional Experience Required
 
 
 
 <ul>
 <li>
 Bachelor s Degree in Health-related Sciences, preferably pharmaceutical area.
 </li>
 <li>
 Post-Graduate Certification in Quality Management.
 </li>
 <li>
 Knowledge of cGMP requirements preferred.
 </li>
 <li>
 Minimum of 4 years of Management or technical leadership experience is required.
 </li>
 <li>
 Minimum of 8 years of related experience in Regulatory Affairs field, including Pharma
 </li>
 <li>
 Manufacturing background, and Final Product importation and exportation experience.
 </li>
 <li>
 Preferably with experience on EMA Regulatory requirements and submissions.
 
 </li>
 </ul>
</div>

Regulatory Affairs Sr. Manager

<div>
 <ul>
 <li>
 Support the implementation of the Compliance Program across all departments, ensuring alignment with corporate and global compliance standards.
 </li>
 <li>
 Assist in conducting risk assessments, monitoring activities, and compliance audits, and follow up on corrective and preventive actions (CAPAs).
 </li>
 <li>
 Facilitates the management of Third Party interacting on behalf of GEPD, coordinating background checks on vendors, preparing comprehensive reports in accordance with due diligence processes.
 </li>
 <li>
 Maintain and update compliance-related documentation, including SOPs, training records, and assurance reports.
 </li>
 <li>
 Coordinate training sessions to promote awareness of ethics, compliance policies.
 </li>
 <li>
 Monitor and report on compliance metrics, highlighting potential gaps or process deviations.
 </li>
 <li>
 Liaise with internal stakeholders (Commercial, HR, Medical Affairs, etc.) to ensure smooth execution of compliance requirements.
 </li>
 <li>
 Provide assistance in preparing for inspections and audits, ensuring readiness and proper documentation.
 </li>
 <li>
 Participate in investigations and documentation of non-compliance events, ensuring corrective actions are tracked and closed.
 </li>
 <li>
 Promote a culture of ethics, integrity, inclusion, and transparency in all business activities.
 </li>
 <li>
 Serve as a point of contact for employees seeking clarification on compliance procedures or reporting obligations.
 </li>
 </ul>
 
 
 Academic &amp; Professional experience required
 
 
 <ul>
 <li>
 Bachelors degree in Pharmacy, Law, Business Administration, or a related discipline.
 </li>
 <li>
 7 plus years of experience in a control function e.g. Medical affairs, Quality, or Regulatory affairs (preferably in the pharmaceutical or healthcare sector), at least 2&ndash;4 years of which is in compliance.
 </li>
 <li>
 Strong understanding of compliance frameworks, SOP management, and audit processes
 </li>
 <li>
 Proficient in Microsoft Office and reporting tools.
 </li>
 <li>
 Very Good English
 </li>
 </ul>
</div>

Corporate Compliance Lead

Glenmark Pharmaceuticals

<div>
 
 
 Position Details:
 
 
 
 Designation: Country Oncology Lead &ndash; Commercial Oncology
 
 
 Business Unit: Oncology
 
 
 Function: Commercial (Sales, Marketing &amp; Business Operations)
 
 
 Location: Egypt/Flexible
 
 
 Reporting to: Country General Manager and dotted line reporting to Global Oncology Head
 
 
 
 
 
 
 Role Overview/Purpose:
 
 
 
 This is a foundational, build-from-the-ground-up leadership role responsible for establishing Glenmark as a credible and competitive oncology player in a priority launch market.
 
 
 The Country Oncology BUD will have end-to-end responsibility for the commercial launch and growth of Glenmark&rsquo;s first innovative oncology assets in-country, including immuno-oncology, antibody&ndash;drug conjugates (ADCs), and targeted therapies (EGFR TKIs).
 
 
 With the first launch planned in &lt;12 months, the role demands a leader who can simultaneously design strategy and execute hands-on, building the organization, shaping the go-to-market model, and ensuring flawless launch readiness &mdash; all while partnering closely with the Country GM and Global Oncology teams.
 
 
 
 
 
 This role combines:
 
 
 &bull;Strategic leadership
 
 
 &bull;Operational intensity
 
 
 &bull;External oncology credibility
 
 
 &bull;A true &ldquo;general manager mindset&rdquo; within oncology
 
 
 
 
 
 
 Overall Job Responsibilities:
 
 
 
 Key Responsibilities
 
 
 1. Country Oncology Strategy &amp; Financial Accountability
 
 
 &bull; Define and lead the country oncology commercial strategy, fully aligned with global oncology franchise priorities and local market realities.
 
 
 &bull; Be accountable for oncology revenue and gross margin delivery, with shared P&amp;L ownership alongside the Country General Manager.
 
 
 &bull; Develop robust forecasts, business plans, and scenario models to support investment decisions. &bull; Represent oncology performance, risks, and opportunities at the Country Leadership Team and to Global Oncology leadership.
 
 
 
 
 
 2. Launch Excellence &amp; Execution Leadership
 
 
 &bull; Own end-to-end launch readiness for first-in-country innovative oncology assets.
 
 
 &bull; Lead integrated launch planning across:
 
 
 &bull; Sales force readiness
 
 
 &bull; Marketing strategy and execution
 
 
 &bull; Market access coordination
 
 
 &bull; Supply and demand planning
 
 
 &bull; Establish clear launch KPIs, uptake milestones, and post-launch optimization plans.
 
 
 &bull; Ensure best-in-class execution for IO, ADC, and targeted therapy launches in a highly competitive environment.
 
 
 
 
 
 3. Organization Build &amp; Commercial Capability Creation
 
 
 &bull; Build the oncology organization from near-zero, including: Sales, Marketing, Business Operations &bull; Define optimal field force size, structure, and deployment model.
 
 
 &bull; Recruit, develop, and retain high-caliber oncology talent with a strong performance culture.
 
 
 &bull; Instill strong governance, compliance, and execution discipline from day one.
 
 
 
 
 
 4. Go-to-Market &amp; Portfolio Management
 
 
 &bull; Design differentiated go-to-market models tailored to tumor types, treatment settings, and customer segments.
 
 
 &bull; Ensure strong alignment across:
 
 
 &squf; Positioning
 
 
 &squf; Pricing and access strategy (in collaboration with access/medical)
 
 
 &squf; Promotional excellence
 
 
 &squf; Omnichannel customer engagement
 
 
 &bull; Drive strong performance of in-line products while preparing the organization for pipeline expansion.
 
 
 
 
 
 5. External Stakeholder &amp; Oncology Ecosystem Leadership
 
 
 &bull; Act as the senior commercial face of Glenmark Oncology in-country.
 
 
 &bull; Build strong relationships with: Key opinion leaders (KOLs) and Oncology societies and networks &bull; Strategic partners and distributors (if applicable)
 
 
 &bull; Partner closely with Medical Affairs on scientific engagement and disease-area shaping.
 
 
 &bull; Support business development, licensing, and alliance activities where relevant at country level.
 
 
 
 
 
 
 Key Relationships/Stakeholders:
 
 
 
 External
 
 
 &bull; Oncology KOLs and treatment centers
 
 
 &bull; Oncology societies and networks
 
 
 &bull; Strategic partners and service providers
 
 
 
 
 
 Internal (other than Direct Reports)
 
 
 &bull; Country General Manager and Country Leadership Team
 
 
 &bull; Global Oncology Franchise &amp; Brand Teams
 
 
 &bull; Country Medical Affairs, Market Access, Regulatory, Finance, and Supply Chain
 
 
 
 
 
 
 Desired Experience and Knowledge:
 
 
 
 Educational Knowledge:
 
 
 &bull; MBA or master&rsquo;s degree in business, Life Sciences, or related field preferred
 
 
 
 
 
 Experience:
 
 
 &bull; 12&ndash;15+ years of pharmaceutical / biotech experience, with a strong focus on innovative oncology.
 
 
 &bull; Proven track record of launching first-in-country innovative oncology products, ideally in solid tumors.
 
 
 &bull; Direct experience across IO, ADCs, and/or targeted therapies (e.g., EGFR TKIs).
 
 
 &bull; Demonstrated success in building and leading oncology teams from scratch or early stage.
 
 
 &bull; Experience operating in complex, fast-evolving oncology markets.
 
 
 &bull; Prior country-level or franchise leadership experience is strongly preferred.
 
 
 
 
 
 Knowledge and Skills (Functional and Technical):
 
 
 &bull; Strong commercial and financial acumen with a GM-like mindset.
 
 
 &bull; Deep understanding of oncology customers, treatment pathways, and competitive dynamics.
 
 
 &bull; Hands-on leader who can move seamlessly between strategy and execution.
 
 
 &bull; Exceptional stakeholder management, influence, and communication skills.
 
 
 &bull; High ethical standards with uncompromising compliance orientation.
 
 
 
 
 
 Why this role is Unique
 
 
 &bull; First-in-country launch of innovative oncology assets
 
 
 &bull; Opportunity to build the oncology business from the ground up
 
 
 &bull; Seat at the Country Leadership Team
 
 
 &bull; Direct impact on Glenmark&rsquo;s transformation into an innovation-led oncology player
 
</div>

Country Oncology Lead– Commercial Oncology

Jamjoom Pharma

<div>
 Jamjoom Pharma is seeking a seasoned legal leader to oversee our legal affairs across international markets. Reporting directly to the Group Legal Director in KSA, you will spearhead legal strategy, corporate governance, and risk management across our international operations&mdash;ensuring legal excellence and business alignment in fast-evolving environments.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Provide strategic legal counsel across multiple jurisdictions, supporting commercial, regulatory, IP, and employment matters
 </li>
 <li>
 Participate in strategic planning forums across countries and clusters, aligning legal input with core business objectives
 </li>
 <li>
 Lead contract lifecycle management and intellectual property oversight including trademarks portfolio
 </li>
 <li>
 Ensure robust governance across subsidiaries, including board resolutions, filings, and policy implementation
 </li>
 <li>
 Advise on legal compliance, risk mitigation, and emerging regulatory matters including cybersecurity and data protection
 </li>
 <li>
 Collaborate with internal stakeholders and manage external counsel for litigation and specialized matters
 
 
 </li>
 </ul>
 
 Qualifications Required
 
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in law
 </li>
 <li>
 Minimum 10 years as in-house counsel
 </li>
 <li>
 Fluent in Arabic and English (written and verbal)
 
 
 </li>
 </ul>
 
 Preferred Qualifications
 
 
 
 <ul>
 <li>
 LLM or equivalent postgraduate legal degree
 </li>
 <li>
 Licensed to practice law in a Middle Eastern jurisdiction
 </li>
 <li>
 Experience within the pharmaceutical or similar regulatory industry
 </li>
 <li>
 Proficiency in French
 </li>
 <li>
 Deep expertise in commercial, contract, and corporate law
 </li>
 <li>
 Strong business acumen and ability to offer commercially sound legal solutions
 </li>
 </ul>
</div>

Senior Legal Manager

AstraZeneca

<div>
 
 Job Title: Nominated Signatory &amp; Medical Excellence Lead
 
 
 
 
 Introduction To Role
 
 
 
 Are you ready to uphold the highest standards of medical governance while accelerating field excellence to deliver better outcomes for patients? This role places you at the center of ethical decision-making and capability building, ensuring that every activity, material, and interaction reflects our standards and enables impact at pace.
 
 
 You will bridge rigorous compliance with practical execution, helping teams move fast and do the right thing. Can you translate strategy into measurable improvements that raise the quality and reach of medical engagement? Join us to combine science, ethics, and operational excellence in a dynamic environment where bold ideas and disciplined delivery go hand in hand.
 
 
 
 Accountabilities
 
 
 
 <ul>
 <li>
 Ethical Interactions Governance: Own and maintain local Ethical Interactions (EI) SOPs; translate global Code of Conduct into robust local procedures covering patient interactions, digital communications, diagnostics, patient affordability, and external funding.
 </li>
 <li>
 Nominated Signatory Leadership: Lead a team of risk assurance managers/signatories; review and approve materials and activities to meet ABAC, data privacy, local regulatory, and company standards; sign HCP/HCO agreements on behalf of the business.
 </li>
 <li>
 External Funding Oversight: Chair the Ethical Interactions Committee; assess, approve, and monitor external funding and third‑party engagements, ensuring transparency, fairness, and appropriate documentation.
 </li>
 <li>
 Risk and Assurance: Conduct first-line monitoring and quality checks; partner with Compliance and Assurance to execute risk assessments, define CAPAs, and track remediation to closure with evidence and sustainability plans.
 </li>
 <li>
 Medical Quality and Standards: Guide medical and marketing collaboration to ensure scientific accuracy, fair balance, and adherence to codes and SOPs across congresses, advisory boards, digital engagement, and field medical activities.
 </li>
 <li>
 Digital Compliance: Govern compliant HCP digital engagement platforms and content, ensuring consent, privacy-by-design, and appropriate content governance across channels.
 </li>
 <li>
 Process Improvement: Drive simplification and continuous improvement of governance processes, templates, and systems; embed controls proportionate to risk while enabling business agility.
 </li>
 <li>
 Cross-Functional Partnership: Advise cross‑functional teams on ethical and governance considerations for complex initiatives, mega events, and interactions with government officials.
 </li>
 <li>
 Medical Excellence: Purpose Elevate Medical Affairs capability across Egypt by defining competency standards, driving robust onboarding and continuous development for Medical Science Liaisons (MSLs) and Medical Advisors, and owning certification and quality assurance to improve scientific engagement, evidence generation readiness, and cross-functional impact.
 </li>
 <li>
 Liaise with the Global &amp; International Medical Excellence Team in connection to excellence programs, localize relevant initiatives to Egypt market as aligned with local strategy and compliance, and seek out opportunities for cross-market collaboration.
 </li>
 <li>
 Improve scientific engagement quality, call planning, narratives, objection handling, compliant interactions, and insight capture/translation.
 </li>
 <li>
 Equip medical managers with coaching requirements as per AZ standards.
 
 
 </li>
 </ul>
 
 Essential Skills/Experience
 
 
 
 <ul>
 <li>
 Education: Bachelor&rsquo;s degree in pharmacy or related life sciences field required.
 </li>
 <li>
 Experience: 7+ years in Medical Affairs/Compliance/Governance within pharma, including direct Nominated Signatory or equivalent approval authority.
 </li>
 <li>
 Expertise: Strong knowledge of ABAC, Data Privacy, EI codes, GxP fundamentals, and Egypt regulatory frameworks; audit and CAPA lifecycle management; digital engagement governance.
 </li>
 <li>
 Risk assessment, SOP authorship, stakeholder management, training design/delivery, analytical problem solving, change management, and clear written/oral communication in English
 
 
 </li>
 </ul>
 
 Desirable Skills/ Experience
 
 
 
 <ul>
 <li>
 Certifications : GCP/GVP quality, compliance auditing, data privacy, or ABAC training.
 </li>
 <li>
 Medical Excellence Manager Experience
 
 
 </li>
 </ul>
 
 Why AstraZeneca
 
 
 
 Join a team that blends scientific rigor with commercial precision to launch innovations that matter to patients, moving from early diagnosis through treatment with an unwavering ethical core. We operate at pace in evolving markets with the freedom to experiment, learn, and improve, bringing surprising combinations of people together to spark bold thinking. We value kindness alongside ambition, and we follow the evidence to deliver solutions that serve patients and the business without compromising on doing the right thing. Your contribution will shape a connected healthcare ecosystem through partnerships and practical innovation, powered by a science-led pipeline that keeps learning fresh and impact real.
 
 
 
 Call To Action
 
 
 
 Step forward to lead medical governance and excellence&mdash;bring your rigor and creativity to power faster, safer decisions and create meaningful patient impact!
 
 
 
 Date Posted
 
 
 
 08-مارس-2026
 
 
 
 Closing Date
 
 
 
 31-مارس-2026
 
 
 AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
</div>

Nominated Signatory & Medical Excellence Lead

Explore 246+ Regulatory affairs sr manager in Cairo this March. Find roles across top companies and apply now to boost your career.

246 regulatory affairs sr manager jobs In Cairo

Regulatory Affairs Sr. Manager

Regulatory Affairs Sr. Manager

Corporate Compliance Lead

Country Oncology Lead– Commercial Oncology

Senior Legal Manager

Senior Legal Manager

Nominated Signatory & Medical Excellence Lead