Pharmacist

Company Description SHIFA Hospital is a modern healthcare facility dedicated to delivering safe, high-quality patient care in New Cairo. The hospital focuses on clinical excellence, adherence to international standards, and continuous improvement of medical and support services. Multidisciplinary teams work together to provide compassionate care and a reliable patient experience. SHIFA Hospital encourages professional growth, structured training, and collaboration across departments to enhance quality and patient safety. Role Description The Quality Specialist is a full-time, on-site role based at SHIFA Hospital in New Cairo. The role involves monitoring and evaluating clinical and non-clinical processes, conducting regular quality audits, and supporting implementation of quality assurance and quality control procedures. The Quality Specialist will collect and analyze data, prepare reports, and help identify trends, risks, and opportunities for improvement. Responsibilities include collaborating with medical and administrative teams, supporting accreditation and compliance activities, and assisting in developing policies, protocols, and training materials related to quality and patient safety. Qualifications Candidates should possess strong Analytical Skills to collect, interpret, and report quality-related data. Candidates should possess Quality Assurance and Quality Control skills to maintain standards and ensure consistent service delivery. Candidates should possess Quality Auditing skills to plan, conduct, and document internal audits and compliance reviews. Candidates should possess effective Communication skills to collaborate with multidisciplinary teams and present findings clearly. Bachelor’s degree in healthcare management, nursing, pharmacy, or a related field; advanced certifications in quality or patient safety are an advantage. Experience in hospital or healthcare quality management, accreditation standards (e.g., JCI or equivalent), and policy implementation is preferred. Strong attention to detail, ability to prioritize tasks, and proficiency with office and data analysis software. Commitment to ethical practice, patient-centered care, and continuous improvement. Show more

Company Description El Ahlyia Healthcare (EHC) is a leading medical supplies distributor that has been serving the Egyptian market since 1995. The company focuses on delivering cutting-edge medical technologies and innovative healthcare solutions to hospitals, clinics, and healthcare providers. EHC has established a strong position in the market and built a solid reputation as a trusted partner in healthcare. The organization is committed to improving people’s lives by ensuring access to high-quality, reliable medical products and services. Joining EHC offers the opportunity to contribute to meaningful work that supports better patient outcomes across Egypt. Role Description The Regulatory Affairs Senior Specialist is a full-time, on-site role based in Cairo, Egypt. This position is responsible for preparing, reviewing, and maintaining regulatory documentation for medical products, ensuring accuracy, completeness, and compliance with local and international regulations. The role includes coordinating and submitting regulatory files and registration dossiers to relevant authorities, tracking approval timelines, and managing renewals and variations. The specialist monitors changes in regulatory requirements, advises internal stakeholders on compliance implications, and supports quality and commercial teams in implementing regulatory policies and procedures. Day-to-day tasks also involve liaising with regulatory bodies, responding to inquiries, supporting audits and inspections, and contributing to continuous improvement of regulatory processes. Qualifications Candidates should possess strong skills in Regulatory Documentation and Regulatory Submissions, including dossier preparation, file compilation, and tracking approvals. Candidates should possess solid expertise in Regulatory Compliance and Regulatory Requirements, with the ability to interpret and apply relevant laws, guidelines, and standards. Candidates should possess foundational knowledge and experience in Regulatory Affairs, covering product registration, post-market changes, and lifecycle management. Bachelor’s degree in Pharmacy, Medicine, Life Sciences, or a related field; an advanced degree or regulatory certification is an advantage. Proven experience in regulatory affairs within medical devices, medical supplies, or pharmaceuticals, preferably in the Egyptian or MENA market. Strong attention to detail, organizational skills, and the ability to manage multiple projects and deadlines. Effective communication skills, with the ability to collaborate with cross-functional teams and interact with regulatory authorities professionally. Proficiency in MS Office and regulatory tracking tools; strong written and spoken English and Arabic skills. Show more

🏢 About Us: generations GENETICS is a scientific institution that harnesses the power of DNA technology to help individuals and families build a healthier future. We are more than just a lab – we are a fully integrated healthcare provider, operating state-of-the-art clinics staffed with professional physicians who specialize in genetic medicine. Our advanced laboratory ensures the highest standards of accuracy and reliability, while our medical team provides expert consultation and personalized care. From prenatal care and newborn screening to diagnosing heritable disorders and personalized medicine, we adopt a holistic approach to genetic health. We are committed to empowering people with the knowledge they need to make informed health decisions. 🧩 Key Responsibilities: Collect blood and other required specimens from patients of all age groups while following approved phlebotomy procedures. Ensure proper labeling, handling, storage, and packaging of samples to maintain specimen integrity before transportation to the main laboratory. Adhere to infection control protocols, safety standards, and quality procedures throughout the sample collection process. Provide a professional and reassuring experience for patients by explaining the collection procedure and addressing their concerns. Maintain accurate documentation and collaborate effectively with the clinical team to ensure efficient patient care and workflow. 🎯 Qualifications & Requirements: Bachelor's degree in Nursing, Agriculture ,or a related healthcare field. 1-3 Proven experience as a phlebotomist or Nurse in a hospital, medical laboratory, or healthcare facility. 🧠 Skills & Competencies: Strong communication and interpersonal skills, with a patient-focused and professional attitude. Ability to manage time effectively, and maintain accuracy and attention to detail. Administrative experience, including computer skills, file management, and clinic organization, is preferred. 📍 Heliopolis, ⏰ 5 days per week – Rotational shifts (8 hours/day, 12PM - 8PM). ✨ What We Offer: Competitive salary package. Social & medical insurance. Annual profit share. Employee happiness program Continuous Training & development Supportive, family-like work environment. Show more

Company Description Tetra Pharma Co. LTD is a growing pharmaceutical company specializing in toll manufacturing services for a wide range of medicinal products. The company focuses on delivering high-quality, compliant, and cost-effective manufacturing solutions to its partners in the pharmaceutical industry. With modern facilities and professional teams, Tetra Pharma supports formulation, production, and packaging activities for various dosage forms. The organization emphasizes regulatory compliance, operational excellence, and continuous improvement to meet evolving market and healthcare needs. Role Description The Pharmaceutical Toll Manufacturing role is a full-time, on-site position based in Qesm Heliopolis. The role involves managing and overseeing toll manufacturing operations, including coordinating production plans, supervising batch execution, and ensuring adherence to quality standards and regulatory requirements. Daily tasks include monitoring compliance with Good Manufacturing Practice (GMP), collaborating with quality control and laboratory teams, and documenting all manufacturing activities accurately. The role also requires interaction with internal stakeholders and external partners to support technical transfers, resolve operational issues, and optimize production efficiency. The individual will contribute to continuous improvement initiatives and support audits and inspections as needed. Qualifications Strong foundation in Pharmacy and Pharmaceuticals, with the ability to apply scientific and technical knowledge in a manufacturing environment. Demonstrated understanding of Good Manufacturing Practice (GMP), including compliance, documentation, and regulatory standards. Laboratory Skills relevant to pharmaceutical production, such as handling raw materials, performing basic tests, and supporting quality control activities. Sales or client-facing experience related to toll manufacturing services, including managing partner expectations and supporting technical discussions. Bachelor’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related field. Experience in pharmaceutical manufacturing or toll production is highly beneficial. Strong attention to detail, organizational skills, and ability to follow standardized procedures and protocols. Effective communication skills and ability to work collaboratively with cross-functional teams on-site. Familiarity with safety regulations and good documentation practices in a pharmaceutical setting. Show more