Remote Pod Lead - Life Science

Company Description Atco Pharma is a well-established pharmaceutical company specializing in both human and veterinary healthcare products and is ranked among the leading industry players in Egypt. The company manufactures its products according to Good Manufacturing Practice (GMP) standards, ensuring high levels of safety and reliability for patients. Atco Pharma also follows ISO standards and was awarded the International Quality Crown Award in 2015 for its commitment to quality and excellence. Guided by a strong understanding of the value of health and well-being, the company focuses on developing therapeutic solutions that reflect these principles. Role Description The Senior Regulatory Specialist – Pharmacist is a full-time, on-site role based in Cairo, Egypt. This position is responsible for preparing, reviewing, and submitting regulatory dossiers for human and veterinary pharmaceutical products in line with local and international requirements. The role includes maintaining up-to-date knowledge of relevant regulations, guidelines, and standards, and ensuring product registration, variations, renewals, and labeling comply with regulatory expectations. The specialist collaborates with cross-functional teams such as R&D, quality assurance, production, and marketing to provide regulatory input throughout the product lifecycle. Daily activities also involve managing regulatory documentation, responding to authority queries, supporting audits and inspections, and contributing to continuous improvement of regulatory processes. Qualifications Strong regulatory affairs expertise, including experience with product registration, variations, renewals, and labeling in the pharmaceutical sector. Solid knowledge of GMP, ISO standards, and relevant national and international regulatory guidelines for human and veterinary medicines. Professional background as a licensed Pharmacist, with a Bachelor’s degree in Pharmacy or a closely related field; advanced certifications in regulatory affairs are an advantage. Proficiency in preparing, organizing, and reviewing technical documentation, dossiers, and regulatory submissions with high attention to detail. Effective communication and collaboration skills for working with multidisciplinary teams and interacting with regulatory authorities. Strong analytical, problem-solving, and time-management abilities, with capacity to handle multiple projects and deadlines. Good command of English and Arabic, both written and spoken; strong computer and documentation management skills. Previous experience in a similar senior regulatory role within a pharmaceutical company is highly desirable. Show more

- خبره في الادويه - يشترط خبره في الجرد و التسليمات وتحضير الطلبيات -يشترط معرفه ببدائل الادويه - يشترط مستوي جيد و معرفه جيده في الاكسل. المواعيد من 9 صباحا حتي 10 مساء شفت 8 ساعات (شفتات متغيره)

FPI Is Hiring | R&D Formulation Supervisor Future Pharmaceutical Industries (FPI) is looking for an experienced and motivated R&D Formulation Supervisor to join our team! 📌 Job Requirements: Bachelor’s degree in Pharmacy. 5–7 years of relevant experience in pharmaceutical formulation and R&D. Strong knowledge of pharmaceutical formulation and product development. Good analytical and problem-solving skills. Strong team management, communication, and organizational skills. 📍 Location: FPI Plant – Badr City, Egypt. 📩 To Apply: Please send your updated CV to hr6@future-eg.com with the subject line: R&D Formulation Supervisor. Show more

Job Summary We are seeking an experienced and highly motivated Senior Consultant – Public Health & Patient Support Programs to lead and support the design, implementation, monitoring, and evaluation of public health initiatives and patient support programs (PSPs). The successful candidate will provide strategic and operational expertise across healthcare projects, collaborating with government entities, healthcare providers, pharmaceutical companies, patient advocacy groups, and other stakeholders to improve patient outcomes and access to care. The Senior Consultant will play a key role in driving program excellence, ensuring compliance with regulatory and quality standards, and delivering measurable health outcomes through innovative, patient-centric solutions. Key Responsibilities Strategic Program Development Lead the design, planning, and implementation of public health programs and patient support initiatives. Conduct healthcare landscape assessments, needs analyses, and stakeholder mapping to identify gaps and opportunities. Develop strategic recommendations to improve patient access, adherence, persistence, and health outcomes. Support business development activities, including proposal development, technical writing, and client presentations. Program & Project Management Oversee end-to-end management of patient support and public health projects, from initiation through closure. Develop project plans, timelines, budgets, risk registers, and governance frameworks. Monitor project performance against agreed KPIs, deliverables, budgets, and timelines. Identify operational challenges and develop mitigation and improvement strategies. Stakeholder & Client Engagement Build and maintain strong relationships with healthcare professionals, government authorities, payers, patient associations, NGOs, and pharmaceutical partners. Facilitate stakeholder meetings, workshops, and advisory boards. Serve as the primary point of contact for clients and key project stakeholders. Monitoring, Evaluation & Reporting Design and implement monitoring and evaluation frameworks for public health and patient support initiatives. Analyze healthcare and program performance data to generate actionable insights. Prepare reports, dashboards, presentations, and executive summaries for clients and leadership. Present project outcomes and recommendations to senior stakeholders. Quality & Compliance Ensure programs comply with local regulations, ethical standards, pharmacovigilance requirements, data privacy regulations, and company SOPs. Support quality assurance activities, audits, and process improvement initiatives. Ensure accurate documentation and maintenance of project records. Team Leadership & Mentorship Provide guidance and mentorship to program managers and project teams. Foster a culture of collaboration, accountability, and continuous improvement. Support resource planning and capability development within the team. Required Qualifications Education Bachelor’s degree in Medicine, Pharmacy, Public Health, Healthcare Management, Life Sciences, or a related field. Master’s degree in Public Health (MPH), Healthcare Management, Epidemiology, or a related discipline is preferred. Experience 7–10 years of professional experience in healthcare consulting, public health programs, patient support programs, healthcare operations, or related healthcare services. Proven experience leading large-scale patient support programs and/or public health projects. Experience working with pharmaceutical companies, governmental healthcare entities, NGOs, healthcare providers, or consulting organizations. Demonstrated success in stakeholder management and client engagement. Required Skills & Competencies Technical Competencies Strong understanding of public health principles and healthcare systems. Experience in patient support program design and implementation. Knowledge of healthcare regulations, pharmacovigilance requirements, and patient privacy standards. Advanced project/program management and governance skills. Strong data analysis, reporting, and performance management capabilities. Professional Skills Excellent strategic thinking and problem-solving abilities. Strong leadership and team management skills. Exceptional communication, presentation, and facilitation skills. Ability to manage multiple projects in a fast-paced environment. Strong client-facing and relationship management capabilities. High attention to detail and commitment to quality. Digital Skills Advanced proficiency in Microsoft Excel, PowerPoint, and Word. Experience with healthcare CRM platforms, project management tools, and reporting dashboards is preferred. Knowledge of business intelligence and data visualization tools is an advantage. Preferred Experience Candidates will ideally have experience in: Designing and managing patient access, adherence, and disease management programs. Working on Ministry of Health, national healthcare, or population health initiatives. Conducting healthcare research, needs assessments, and program evaluations. Managing cross-functional teams and multi-stakeholder healthcare projects. Supporting healthcare transformation and patient-centric care initiatives. Key Success Indicators Success In This Role Will Be Measured Through Successful delivery of projects within scope, timeline, and budget. Achievement of defined program KPIs and patient outcomes. High levels of client satisfaction and stakeholder engagement. Effective risk management and issue resolution. Continuous improvement and innovation across program operations. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. Show more