Pharmacist Assistant Jobs in Egypt
4204 Jobs Found
Job purpose:To manage the complete lifecycle of an assigned pharmaceutical product or portfolio, from strategic planning to tactical execution. This role is responsible for developing and implementing marketing plans to achieve sales, market share, and profitability goals for the brand.<br>Key accountabilities and decision ownership:Develop and execute the annual brand plan, including marketing strategies, promotional campaigns, and budget allocation. Conduct market analysis, monitor competitor activities, and identify customer insights to drive brand strategy. Collaborate with the sales team to develop promotional materials and provide training to ensure effective delivery of messages. Coordinate with internal cross function teams (Sales, Medical, Finance, Regulatory, Supply Chain) to ensure timely execution of marketing activities. Work with advertising agencies and other vendors to create and implement marketing campaigns across multiple channels. Drive successful new product launches and lifecycle management across the portfolio through product expansion and development. Manage the brand's P&L, including forecasting sales, managing the marketing budget, and tracking performance against KPIs. Engage with Key Opinion Leaders (KOLs) to gather insights and support brand advocacy.<br>Specifications of job holder<br>Functional Competencies Proficiency Level:Brand Planning & Strategy: Advanced Market Analysis: Advanced Marketing Campaign Execution: Advanced Financial Acumen (P&L Management): Intermediate Cross-Functional Collaboration: Advanced<br>Leadership Competencies Proficiency Level:Strategic Thinking: Intermediate Project Management: Advanced Influence & Communication: Advanced Analytical Skills: Advanced<br>Must have technical / professional qualifications:<br>Academic, technical, and professional qualifications: Bachelor’s degree in pharmacy, medical related field, or Marketing. Minimum 3-5 years of experience in pharmaceutical marketing or sales Direct experience as a Product Manager or Associate Product Manager is required.<br>Skills: Analytical Skills: Advanced Project Management: Advanced Communication & Presentation: Advanced Digital Marketing Tools: Intermediate
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<p><b>Strategic Oncology Account Director - Southeast - FL and Puerto Rico.</b></p><br><br><br><p><b>GSK ONCOLOGY</b></p><br><br><p>GSK is a place to build a career in Oncology where purpose, science and growth come together. As a focused, global biopharma company, we unite science, technology, and talent to get ahead of disease together — with a clear ambition to deliver impact for patients at scale.</p><br><br><p>For people looking to make a difference, that means joining a company with the capabilities, investment and momentum to translate innovation into meaningful improvements in patient outcomes — and to do it as part of a business entering a sustained period of growth.</p><br><br><br><p>GSK Oncology is building real momentum — advancing a growing portfolio of approved medicines while investing in a pipeline designed to redefine cancer care. Recent progress, including approvals in endometrial cancer and multiple myeloma, alongside targeted business development to expand into areas such as lung cancer, reflects a business that is delivering today while building for the future.</p><br><br><p>What sets GSK apart is the combination of scientific depth and culture. With substantial investment in R&D, a broad development pipeline, expertise in genetics and advanced technologies, and a strong partnership model, GSK offers the opportunity to work at the forefront of innovation.</p><br><br><p>Just as importantly, GSK is a place where people can thrive. Our culture is grounded in being ambitious for patients, accountable for impact, and committed to doing the right thing — creating an environment where individuals are supported to grow and contribute at their full potential. </p><br><br><p>For talent in Oncology, GSK offers the opportunity to be part of a science‑led, high‑growth business — contributing to work that is shaping the future of cancer care and making a meaningful difference for patients.</p><br><br><br><p><b>ROLE SUMMARY:</b></p><br><br><p>The Strategic Oncology Account Director serves as the primary strategic lead to complex oncology provider accounts across academics, health systems, free-standing cancer centers, and community oncology practices. This role bridges clinical, economic, and operational execution to advance GSK goals in Oncology, including access and account strategies that remove access barriers and deliver growth. </p><br><br><br><p>The Strategic Oncology Account Director develops and executes multi-stakeholder account plans that generate durable institutional adoption, formulary, and on-label access to our therapies. This role requires fluency across clinical science, real-world evidence, healthcare economics, and oncology practice operations—and the executive presence to engage C-suite, clinical leadership, and pharmacy decision makers with equal credibility.</p><br><br><br><p><b>KEY RESPONSIBILITIES:</b></p><br><br><ul><li><p>Develop and maintain trusted relationships with key Population Based Decision Makers (PBDM) (P&T committee, clinical and pharmacy leaders among others) across assigned academic cancer centers, IDNs and community oncology accounts</p><br><br></li><li><p>Support in-field regional engagement with cross-functional field partners, working closely with your partner RSDs on account plans and execution</p><br><br></li><li><p>Deliver clinical value prop discussions on mechanism of action, clinical trial data, safety profiles, and patient selection criteria for portfolio products</p><br><br></li><li><p>Deliver total cost-of-care analyses, including comparative effectiveness, toxicity burden, and administration cost modeling with close input into approved material development with Market Access strategy teams</p><br><br></li><li><p>Support on-label formulary, EHR and pathway inclusion to GSK products</p><br><br></li><li><p>As appropriate, negotiate and pull through contract agreements aligned to access and customer strategies</p><br><br></li><li><p>Identify pain points within the account across clinical, economic, and operational execution related to GSK brands and work with cross-functional partners to appropriately address</p><br><br></li><li><p>Build a regular cadence of business reviews, executive exchanges and clinical education sessions with pharmacy and clinical leadership</p><br><br></li><li><p>Represent GSK at sponsored industry events, with proper planning, execution, and follow-up</p><br><br></li><li><p>Own enterprise-level relationships and lead on access strategies for our products for priority accounts, mapping influence hierarchies across academic cancer centers, IDNs and community practice networks and keep updated regularly</p><br><br></li><li><p>Lead and coordinate cross-functional account planning (Medical Affairs, Market Access, Patient Services, BU Sales, GPO lead) to present a unified engagement strategy</p><br><br></li><li><p>Identify opportunities to support broader account engagement that align with institutional priorities and portfolio positioning and, when needed, facilitate appropriate hand-offs internally</p><br><br></li><li><p>Accurately forecast business performance by account and maintain CRM records with discipline and precision</p><br><br></li><li><p>Contribute competitive intelligence, field insights, and account dynamics to inform regional and national commercial strategy</p><br><br></li></ul><br><p><b>Basic Qualifications:</b></p><br><br><ul><li><p>Bachelor’s Degree</p><br><br></li><li><p>8+ years in pharmaceutical/biotech commercial roles</p><br><br></li><li><p>4+ years in pharmaceutical/biotech commercial roles working in Oncology</p><br><br></li><li><p>Account management experience in complex settings (E.G., Academic, IDN Accounts, or Community Provider Networks) at the enterprise (C/D suite) level</p><br><br></li></ul><br><p><b>Preferred Qualifications:</b></p><br><br><ul><li><p>Experience in solid tumor and/or hematologic malignancy therapeutic areas</p><br><br></li><li><p>Familiarity with community oncology practice management, GPO relationships and oncology group purchasing dynamics</p><br><br></li><li><p>Experience working with oncology care models, value-based contracts, or risk-bearing provider groups</p><br><br></li><li><p>Prior cross-functional roles in Market Access, Sales Leadership, Medical Affairs, or HEOR</p><br><br></li><li><p>Demonstrated clinical fluency including the ability to discuss oncology clinical trial data, pathology, biomarker testing, and treatment algorithms with key stakeholders</p><br><br></li><li><p>Economic acumen including a working knowledge of oncology reimbursement, 340B program, GPO contracting, buy-and-bill, and specialty pharmacy dynamics</p><br><br></li><li><p>Experience supporting or leading a pharmaceutical oncolytic product launch</p><br><br></li><li><p>Experience using MS Office Suite, Veeva CRM, and Power BI or equivalent analytics platforms</p><br><br></li></ul><br><p>#GSKOncology 2026</p><br><br><p>#LI-GSK</p><br><br><br><p><b>Skills</b></p><br><br>Account Management, Cross-Functional Work, Data to Insights, Digital Fluency, Omnichannel, Scientific Literacy<br><br><br><p>Please visit <span><u>GSK US Benefits Summary</u></span> to learn more about the comprehensive benefits program GSK offers US employees. </p><br><br><br><br><p><b>Why GSK?</b></p><br><br><p><b>Uniting science, technology and talent to get ahead of disease together.</b></p><br><br><br><p>GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.</p><br><br><br><p>People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.</p><br><br><br><p><span>If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at - </span><span><u>usrecruitment.adjustments@gsk.com</u></span> </p><br><br><br><p>GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.</p><br><br><br><p><b>Important notice to Employment businesses/ Agencies</b></p><br><br><p>GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.</p><br><br><br><p>Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <span><u>https://openpaymentsdata.cms.gov/</u></span></p><br><br><br> </div>
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<span>TJM Labs builds AI-driven automation that strips away the repetitive, error-prone tasks slowing pharmacies down so teams can focus on patient care.<br> Our bots handle prescription intake, fax processing, insurance workflows and more, helping pharmacies scale efficiently without adding headcount.<br> TJM Labs is looking for a Full Stack Engineer to join our growing team.<br> This is an excellent opportunity for someone early in their software engineering career who enjoys solving problems, building thoughtful solutions, and learning quickly in a fast-paced remote environment.<br> We’re less focused on where you went to school or how many years of experience you have, and more interested in how you think, how you work, and your potential to grow.<br> As a Full Stack Engineer, you’ll support the development of internal tools, automations, and software products that help drive our business forward.<br> You’ll work closely with technical team members to build practical solutions, troubleshoot issues, and contribute to ongoing product improvements.<br> What You'll Do Design, build, and maintain software applications, services, and internal tools.<br> Develop new automation solutions and product features for pharmacy workflows.<br> Build and maintain integrations with third-party systems and APIs.<br> Troubleshoot production issues and improve system reliability and performance.<br> Write clean, maintainable, and well-tested code.<br> Participate in code reviews and technical discussions.<br> Collaborate with teammates to plan, scope, and deliver projects.<br> Use modern development tools, including AI-assisted workflows, to improve productivity and software quality.<br> Identify opportunities to simplify processes and improve engineering efficiency.<br> Contribute to architecture and technical design decisions as the platform grows.<br> Follow secure coding practices, protect company data, and adhere to internal information security policies and procedures.<br> Fully remote work environment.<br> Competitive compensation.<br> Meaningful projects with direct business impact.<br> High ownership and autonomy.<br> Opportunity to work with AI-driven technologies and modern development tools.<br> A collaborative team focused on solving real problems for healthcare customers.<br> 3+ years of software development experience.<br> Strong experience with Python.<br> Experience building web applications, APIs, or backend systems.<br> Experience with Git, GitHub, and modern software development workflows.<br> Familiarity with databases and data modeling.<br> Strong debugging, troubleshooting, and problem-solving skills.<br> Ability to work independently in a remote environment.<br> Clear written and verbal English communication skills.<br> Strong sense of ownership and accountability.<br> Nice to Have Experience with JavaScript, TypeScript, React, or modern frontend frameworks.<br> Experience building AI-powered applications, automations, or workflow systems.<br> Experience working with cloud infrastructure and deployment pipelines.<br> Experience integrating with third-party platforms and APIs.<br> Familiarity with healthcare technology or regulated industries.<br> Experience working at a startup or high-growth company.<br></span> </div>
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<b>Job Description</b><p>Job Description </p><br><p>AtkinsRéalis Global Technology Centre (GTC) Middle East Business is looking to appoint a MECH BIM Lead / Senior BIM Engineer / Assistant Technical Manager to support the delivery of complex Mechanical engineering and multidisciplinary designs across a range of major projects. </p><br><p>As the MECH BIM Lead / Senior BIM Engineer / Assistant Technical Manager you will lead a team of BIM engineers and modelers with the responsibility for guiding this team on all technical matters and perform multi discipline design management and coordination. You will be an experienced practitioner of BIM / Digital technologies, with proven track record of applying these technologies to develop engineering solutions. </p><br><p>This key post will be based on Cairo where we have thriving AtkinsRéalis office, which serve all AtkinsRéalis regions across the world. Our portfolio of work continues to grow, and we will offer a challenging and rewarding opportunity to apply knowledge, experience and problem-solving skills. </p><br><p>Your role</p><br><ul><li>MECH BIM lead experience working on multi-D projects. </li></ul><ul><li>Should have in depth knowledge on MECH systems and how its constructed in site. </li></ul><ul><li>Should have in-depth knowledge on all the latest CDE's. </li></ul><ul><li>Should have in-depth knowledge on ISO19650. </li></ul><ul><li>To collaborate with Designers, BIM leads, Planners to ensure alignment and quality BIM models. </li></ul><ul><li>Develop documentation required to support the implementation and progression of 3D & 4D BIM. </li></ul><ul><li>Should be well versed with Revit MECH & AutoCAD and able to mentor team. </li></ul><ul><li>Follow firm-wide BIM/CAD Standards, procedures and guidelines that conform to international standards, our firm's culture, and the emerging best practices. </li></ul><ul><li>Model/drawing set-up and organize. </li></ul><ul><li>Preparing 3D REVIT MECH Models, Families and Schedules. </li></ul><ul><li>Ability to create Parametric Components and vary the value of parameters assigned to groups. </li></ul><ul><li>Coordinate MEP Models with Structural and Architectural Model. </li></ul><ul><li>Able to coordinate and analyse REVIT/Navisworks clash detection reports and correct issues. </li></ul><ul><li>Coordinates work with other disciplines including Electrical, Architectural, Structural and Interior Design. </li></ul><ul><li>Prepares detailed equipment room layouts, detailed riser diagrams, plot files, PDF's, partplans. </li></ul><ul><li>Highlights completed mark-ups and return drawings to Engineer/Manager. Prints drawing sets as requested. </li></ul><ul><li>Checks drawings for quality control using standard checklist, as appropriate. </li></ul><ul><li>Maintains design files in an organized and up-to-date fashion in accordance with company standards. </li></ul><ul><li>Communicates regularly with team to ensure schedules are met. </li></ul><ul><li>Identifies and reports to Manager any project related quality, speed or scheduling issues. </li></ul><p><i>Digital Skills:</i> </p><br><ul><li>Drive technical excellence in Digital production/delivery. </li></ul><ul><li>Support the transition away from using Revit as merely a production/drafting package to a platform that is leveraged for design /engineering (and one that the team lives & breathes). </li></ul><ul><li>Promote and cultivate a more progressive style of design and communication within the team (using alternative digital tools - Rhino/ Grasshopper/CFD/Adobe Suite). </li></ul><ul><li>Dramatically enhance the output of deliverables (visually & speed of service) putting us on a level playing field with our architectural colleagues. </li></ul><ul><li>Promote the team's emerging digital initiative within AtkinsRéalis and externally, with an eye to winning work based on the developing capability and enhancing the brand. </li></ul><p>About you </p><br><p><i>Required skills and Experience:</i> </p><br><ul><li>Bachelor of Engineering with minimum 10-15 years of relevant experience. </li></ul><ul><li>Knowledge of multidisciplinary and multiregional project to comply with the relevant CAD/BIM Standard. </li></ul><ul><li>Ability to read & interpret engineering drawings & specifications. </li></ul><ul><li>Ability to work using Engineers calculations and design in producing drawings / 3D modelling. </li></ul><ul><li>Knowledge of Building design processes working within a multiple discipline engineering environment, and within a project and commercially focused business. </li></ul><ul><li>Identify, interpret and apply required industry/ client/ internal CAD/BIM standards. To ensure that our finished product is Project, Client and BIM compliant. </li></ul><ul><li>Work independently and take proactive initiative. </li></ul><ul><li>Self-motivated development. </li></ul><ul><li>Competent to check the work. </li></ul><ul><li>Able to present / represent their technical work. </li></ul><ul><li>Working knowledge of standard codes and EDMS (Electronic Data Management System. </li></ul><ul><li>Shows flexibility in work tasks and locations. </li></ul><ul><li>Responsible for completion of specifically assigned tasks to time and cost. </li></ul><ul><li>Required Skills for Digital Part. </li></ul><ul><li>A thorough understanding of the data, information management and BIM including compliance to ISO 19650 standards. </li></ul><ul><li>Sound knowledge in engineering design and to assist design team in Self/Inter disciplinary. </li></ul><ul><li>services coordination, quality compliance etc. </li></ul><ul><li>Expert knowledge of BIM authoring tools from various software providers such as Autodesk, Bentley in delivery of multi-disciplinary projects. </li></ul><ul><li>Expert knowledge of model federation and co-ordination platforms such as Navisworks, Revizto, BIM Track (New forma Konekt) for performing tasks like clash detection and resolution, model walkthrough and issue tracking and management. </li></ul><ul><li>Expert knowledge of Common Data Environment (CDE) such as BIM360, ACC and ProjectWise. </li></ul><ul><li>Knowledge of automation tools such as Dynamo. </li></ul><ul><li>Ability to develop technical documentation for Information Management/BIM. </li></ul><ul><li>Effective communication, coordination and collaboration skills. </li></ul><ul><li>Excellent problem-solving and critical thinking skills. </li></ul><ul><li>Desirable Skills and Experience: </li></ul><ul><li>Professional accreditation to the level of an Incorporated or Chartered Engineer or working towards professional qualifications. </li></ul><ul><li>Must be an advanced user or expert user in Autodesk Navisworks with capabilities to federate individual discipline BIM Models. Setup, maintain and run clash rules and clash tests across federated BIM Models. Must know how to create search sets, query, find and navigate through BIM Models. </li></ul><ul><li>Must be able to use Navisworks to generate clash results, manage clash resolution, redline BIM Models, capture viewpoints and cascade reports to discipline teams. Must be able to perform Navisworks model management. </li></ul><ul><li>Computational / Generative design tool experience such as Autodesk Dynamo or Grasshopper / Rhino. </li></ul><ul><li>Technical proficiency in the use of the latest common CDE systems: Bentley ProjectWise and Autodesk BIM360. </li></ul><p><i>Required attributes: </i> </p><br><ul><li>High performing ability to work and integrate into multi-disciplinary teams and work independently. Ensuring your work is to the highest appropriate standards and in compliance with AtkinsRéalis quality systems and standards. </li></ul><ul><li>Energetic and enthusiastic, with the desire to take on extra responsibilities and constantly upskilling team and oneself. </li></ul><ul><li>Excellent written and spoken English communication within a business environment. </li></ul><ul><li>Ability to exercise initiative, take ownership of project issues and work independently with excellent time management skills. </li></ul><ul><li>You will demonstrate a high level of commitment, flexibility and be eager to accept responsibility and learn new skills, whilst always exercising an active interest in helping to solve technical problems faced by any member of the team. </li></ul><ul><li>You will act with integrity and professionalism, gaining the trust of colleagues and setting an example to junior staff. </li></ul><p>Rewards & benefits </p><br><p>Explore the rewards and benefits that help you thrive – at every stage of your life and your career. </p><br><p>This includes: </p><br><p>• Comprehensive life insurance coverage </p><br><p>• Medical insurance for you and your dependents </p><br><p>• Annual leave balance in accordance with local labour law </p><br><p>• Flexible and hybrid work solutions </p><br><p>• Opportunity for local and global internal transfers </p><br><p>• Company gratuity scheme </p><br><p>• Discretionary bonus program </p><br><p>• Employee Wellbeing Program: 24/7 access to specialists in finance, legal matters, family care, personal health, fitness, and nutrition </p><br><p>Seize every opportunity to sharpen your skills, expand your expertise, and be recognized for the impact you make. </p><br><p>About AtkinsRéalis </p><br><p>We're AtkinsRéalis, a world-class engineering services and nuclear organization. We connect people, data and technology to transform the world's infrastructure and energy systems. Together, with our industry partners and clients, and our global team of consultants, designers, engineers and project managers, we can change the world. We're committed to leading our clients across our various end markets to engineer a better future for our planet and its people. </p><br><p>Find out more. </p><br><p>Best Regards</p><br><p><b>Yasser M. Adam</b> </p><br><p><b>AtkinsRéalis</b></p><br><p>A photo of the podcast recording discussing future mobility in the Middle East Watch the podcast</p><br><p>Balados</p><br><p>Au-delà du génie</p><br><p>Carrières</p><br><p>Podcasts</p><br><p>Beyond Engineering</p><br><p>Careers</p><br><p><i>À AtkinsRéalis, nous travaillons selon des horaires flexibles partout dans le monde. Ce courriel a été envoyé à un moment propice pour moi, mais je ne m’attends à une réponse de votre part qu’au moment qui vous conviendra.</i> | <i>At AtkinsRéalis, we work flexible hours around the world. Although I have sent this email at a time convenient for me, I don’t expect you to respond until it works for you.</i></p><br><b>Worker Type</b>Employee<b>Job Type</b>Regular<p><span><i>At </i></span> <i><span>AtkinsRéalis</span></i><span><i>, we seek to hire individuals with diverse characteristics, backgrounds and perspectives. We strongly believe that world-class talent makes no distinctions based on gender, ethnic or national origin, sexual identity and orientation, age, religion or disability, but enriches itself through these differences. </i></span></p><br> </div>
<ul><li><p>Review and verify medical records for accuracy and completeness.</p></li><li><p>Identify, address, and report any discrepancies, issues, or errors found in medical documentation.</p></li><li><p>Analyze and validate medical data to ensure consistency and compliance with regulatory and organizational requirements.</p></li><li><p>Coordinate with healthcare professionals to clarify and resolve documentation issues when necessary.</p></li><li><p>Collect blood samples from patients for laboratory analysis while following proper clinical and safety procedures.</p></li></ul><p></p><p><strong>Requirements</strong></p><ul><li><p>Bachelor’s degree in Medicine, Nursing, Pharmacy, Medical Laboratory Sciences, or a related healthcare field.</p></li><li><p>Previous experience in medical record review, clinical documentation, laboratory work, or healthcare operations is preferred.</p></li><li><p>Strong knowledge of medical terminology, clinical procedures, and healthcare documentation standards.</p></li><li><p>Ability to analyze medical data with high attention to detail and accuracy.</p></li><li><p>Familiarity with healthcare regulations, patient confidentiality, and compliance standards.</p></li><li><p>Excellent organizational, analytical, and problem-solving skills.</p></li><li><p>Good communication and interpersonal skills.</p></li><li><p>Ability to work independently and manage multiple tasks efficiently.</p></li><li><p>Proficiency in Microsoft Office applications and electronic medical record (EMR) systems is an advantage.</p></li><li><p>Experience in blood sample collection and phlebotomy procedures is preferred.</p></li><li><p>Strong commitment to patient safety and professional ethics.</p></li></ul><p></p>
<p>Omega Pharma is seeking a motivated Research & Development (R&D) Specialist to join our growing team. The successful candidate will contribute to the development and optimization of pharmaceutical formulations while supporting product scale-up, technology transfer, and regulatory documentation.</p><p>Key Responsibilities:</p><p>* Develop and optimize pharmaceutical formulations for human and veterinary products.</p><p>* Conduct laboratory trials and prepare technical documentation (BMR, MFR, Formulation Sheets).</p><p>* Perform product scale-up and support technology transfer to manufacturing sites.</p><p>* Evaluate raw materials and Active Pharmaceutical Ingredients (APIs).</p><p>* Support stability studies and prepare regulatory documentation.</p><p>* Collaborate with QA, RA, Production, and Toll Manufacturing teams to ensure successful project execution.</p><p>* Ensure compliance with GMP and company quality standard</p><p><strong>Requirements</strong></p><p>Bachelor’s degree in Pharmacy or a related scientific field.</p><p>* 1–3 years of experience in Pharmaceutical Research & Development.</p><p>* Experience in formulation development of pharmaceutical dosage forms.</p><p>* Good knowledge of oral solid and liquid dosage forms is preferred.</p><p>* Familiarity with GMP requirements and pharmaceutical documentation.</p><p>* Good command of English.</p><p>* Proficiency in Microsoft Office.</p><p>* Strong analytical, documentation, communication, and time management skills.</p><p>* Ability to work effectively within a cross-functional team.</p>
<ul><li><p>Responsible for preparation of Registration dossiers of all new products and Re-registered products.</p></li><li><p>Submitting variations of existing products.</p></li><li><p>Responsible for preparation and submission of Analytical dossiers to NODCAR ( National Organization for Drug Control and Research ).</p></li><li><p>Follow up submission and any supporting documents along with registration lead time.</p></li><li><p>Support logistic team with all references, legalized certificates and material needed for regular analysis and release.</p></li><li><p>Prepare analytical files to be submitted to different authorized labs</p></li><li><p>Follow up analysis and supply all needed requirements to get release certificates f samples.</p></li><li><p>Ensures confidentiality in respect of registration files contents.</p></li><li><p>Completing all registration requirements for all shipments at EDA.</p></li><li><p>Responsible for obtaining Ministry of Health importation approvals, inspection & release.</p></li></ul><p></p><p><strong>Requirements</strong></p><ul><li><p>Bachelor’s degree in Science, pharmacy or vet medicine.</p></li><li><p>Knowledge of EDA regulatory affairs is a must.</p></li><li><p>Hands-on experience in medical devices registration is a must</p></li><li><p>Experience mainly in sterile medical devices regulatory and submissions in CAPA, NODCAR.</p></li><li><p>Good knowledge of preparation of registration files.</p></li><li><p>Excellent command of English and Arabic</p></li><li><p>1-3 years of experience.</p></li></ul><p></p>
<p><strong>Calculate the needs of raw materials and packaging materials necessary to implement the production plan.</strong></p><p><strong>• Issuing purchasing orders, sending them for purchases, and following up on supply.</strong></p><p><strong>• Issuing reports of the required quantities of goods and samples and comparison between the port and the export port.</strong></p><p>Determine the quantities required to be manufactured and review them with the planning manager.</p><p>• Calculating the raw materials and packaging materials required to implement the sales plan on a monthly, quarterly and annual basis.</p><p>• Issuing need orders on Oracle and following them up with purchases after their approval by the department director and the sector head.</p><p>• Issuing lists of new products and approving them from the concerned departments.</p><p>• Follow up on Rameda’s products requirement and produce it in external factories (TOLL out).</p><p>• Supervision the implementation of ISO rules (ISO 9001, ISO 14001/2015, and ISO 45001/2018).</p><p><strong>Requirements</strong></p><ul><li><p>1-3 years of experience</p></li><li><p>Bachelor degree of pharmacy or Science</p></li><li><p>pharmaceutical background is must </p></li><li><p>Excellent analytical skills</p></li><li><p>Excellent communication skills</p></li><li><p>Problem solving skills</p></li><li><p>Use Oracle system</p></li><li><p>Excellent leader ship</p></li></ul><p></p><p></p>
<p><strong>Calculate the needs of raw materials and packaging materials necessary to implement the production plan.</strong></p><p><strong>• Issuing purchasing orders, sending them for purchases, and following up on supply.</strong></p><p><strong>• Issuing reports of the required quantities of goods and samples and comparison between the port and the export port.</strong></p><p>Determine the quantities required to be manufactured and review them with the planning manager.</p><p>• Calculating the raw materials and packaging materials required to implement the sales plan on a monthly, quarterly and annual basis.</p><p>• Issuing need orders on Oracle and following them up with purchases after their approval by the department director and the sector head.</p><p>• Issuing lists of new products and approving them from the concerned departments.</p><p>• Follow up on Rameda’s products requirement and produce it in external factories (TOLL out).</p><p>• Supervision the implementation of ISO rules (ISO 9001, ISO 14001/2015, and ISO 45001/2018).</p><p><strong>Requirements</strong></p><ul><li><p>1-3 years of experience</p></li><li><p>Bachelor degree of pharmacy or Science</p></li><li><p>pharmaceutical background is must </p></li><li><p>Excellent analytical skills</p></li><li><p>Excellent communication skills</p></li><li><p>Problem solving skills</p></li><li><p>Use Oracle system</p></li><li><p>Excellent leader ship</p></li></ul><p></p><p></p>
<p><strong>Calculate the needs of raw materials and packaging materials necessary to implement the production plan.</strong></p><p><strong>• Issuing purchasing orders, sending them for purchases, and following up on supply.</strong></p><p><strong>• Issuing reports of the required quantities of goods and samples and comparison between the port and the export port.</strong></p><p>Determine the quantities required to be manufactured and review them with the planning manager.</p><p>• Calculating the raw materials and packaging materials required to implement the sales plan on a monthly, quarterly and annual basis.</p><p>• Issuing need orders on Oracle and following them up with purchases after their approval by the department director and the sector head.</p><p>• Issuing lists of new products and approving them from the concerned departments.</p><p>• Follow up on Rameda’s products requirement and produce it in external factories (TOLL out).</p><p>• Supervision the implementation of ISO rules (ISO 9001, ISO 14001/2015, and ISO 45001/2018).</p><p><strong>Requirements</strong></p><ul><li><p>1-3 years of experience</p></li><li><p>Bachelor degree of pharmacy or Science</p></li><li><p>pharmaceutical background is must </p></li><li><p>Excellent analytical skills</p></li><li><p>Excellent communication skills</p></li><li><p>Problem solving skills</p></li><li><p>Use Oracle system</p></li><li><p>Excellent leader ship</p></li></ul><p></p><p></p>
<p><strong>Calculate the needs of raw materials and packaging materials necessary to implement the production plan.</strong></p><p><strong>• Issuing purchasing orders, sending them for purchases, and following up on supply.</strong></p><p><strong>• Issuing reports of the required quantities of goods and samples and comparison between the port and the export port.</strong></p><p>Determine the quantities required to be manufactured and review them with the planning manager.</p><p>• Calculating the raw materials and packaging materials required to implement the sales plan on a monthly, quarterly and annual basis.</p><p>• Issuing need orders on Oracle and following them up with purchases after their approval by the department director and the sector head.</p><p>• Issuing lists of new products and approving them from the concerned departments.</p><p>• Follow up on Rameda’s products requirement and produce it in external factories (TOLL out).</p><p>• Supervision the implementation of ISO rules (ISO 9001, ISO 14001/2015, and ISO 45001/2018).</p><p><strong>Requirements</strong></p><ul><li><p>1-3 years of experience</p></li><li><p>Bachelor degree of pharmacy or Science</p></li><li><p>pharmaceutical background is must </p></li><li><p>Excellent analytical skills</p></li><li><p>Excellent communication skills</p></li><li><p>Problem solving skills</p></li><li><p>Use Oracle system</p></li><li><p>Excellent leader ship</p></li></ul><p></p><p></p>
<ul><li><p><strong>Warehouse Operations:</strong> Manage day-to-day activities including receiving, put-away, inventory storage, order picking/packing, and shipping.</p></li><li><p><strong>Process Optimization:</strong> Identify operational bottlenecks and implement lean warehouse strategies to increase throughput and efficiency.</p></li><li><p><strong>Inventory Control:</strong> Conduct regular cycle counts and stock audits to maintain accurate inventory levels and minimize shrinkage/discrepancies.</p></li><li><p><strong>Team Leadership & Safety:</strong> Lead, train, and supervise warehouse personnel while enforcing strict health, safety, and compliance standards.</p></li><li><p><strong>Logistics & Order Fulfillment:</strong> Ensure timely, accurate order processing and coordinate with logistics partners for dispatch and delivery schedules.</p></li><li><p><strong>Reporting & Performance Tracking:</strong> Monitor and report key performance indicators (KPIs) such as order accuracy, space utilization, and fulfillment turnaround times.</p></li></ul><p><br></p><p><strong>Requirements</strong></p><p></p><ul><li><p><strong>Education (Mandatory):</strong> Bachelor's degree in Pharmacy (B.Pharm).</p></li><li><p><strong>Experience (Mandatory):</strong> 5–7 years of experience in pharmaceutical warehousing, logistics, or medicine distribution platforms.</p></li><li><p><strong>Regulatory Knowledge:</strong> Strong understanding of Good Storage & Distribution Practices and MOH/Drug Authority standards.</p></li><li><p><strong>Technical Skills:</strong> Proficiency with Warehouse Management Systems (WMS), ERP tools (e.g., SAP, Oracle), and advanced Excel functions.</p></li><li><p><strong>Leadership & Accuracy:</strong> Excellent leadership, problem-solving abilities, and high attention to detail.</p></li></ul><p></p>
<p>Duties & Responsibilities: Conducting regular investigations to guarantee that workers follow safety procedures as required Conducting quality audits as required to ensure compliance with GMP, Quality standards. Performing pre and post-production quality checks and providing related reports accordingly. Carrying out the issuance and weighing process of raw materials to guarantee the conformity of specifications to quality standards, approving the release of materials to production, as well as ensuring compliance of raw material storage with regulatory guidelines Ensuring compliance of plant conditions (Humidity, Temperature, etc) with set guidelines Checking machine conformity to standards as well as ensuring periodic maintenance implementation Performing other duties related to the job as assigned by the direct supervisor Job Location: 6th of October City</p><p><strong>Desired Candidate Profile</strong></p><p><strong>Job Requirements</strong></p><p>Bachelor s degree in pharmacy with grade Very good or Excellent</p><p>Fresh graduate.</p><p>Ability to work with a team and being an effective team member</p><p>Good understanding in the QA processes and the Agile development process</p><p>Knowledge of quality assurance terminology, methods, and tools</p>
<p> Key Responsibilities: Develop and implement KPIs and performance frameworks to measure and enhance sales force effectiveness and productivity. Analyze sales performance using Power BI, Advanced Excel, CRM platforms, and IQVIA data to identify trends, gaps, and opportunities. Generate actionable, data-driven insights and recommendations to support commercial decision-making, business growth, and operational efficiency. Standardize performance reporting across regions and enhance CRM adoption through effective customer segmentation, engagement tracking, and digital touchpoints. Partner with Sales, Marketing, Finance, and Commercial leadership to optimize market coverage, resource allocation, and Sales Force Effectiveness strategies.</p><p><strong>Desired Candidate Profile</strong></p><p>Bachelor s degree in pharmacy, Business, Data Analytics, or a related field. 3-5 years of experience in Sales Force Effectiveness, Commercial Excellence, Business Analytics, or a similar role, preferably within the pharmaceutical or healthcare industry. Strong analytical skills with hands-on experience in Advanced Excel, Power BI, CRM platforms, and IQVIA/IMS data. Experience in pharmaceutical sales operations, performance management, market analysis, or business intelligence. Strong communication and presentation skills, with the ability to translate complex data into clear insights and actionable business recommendations.</p>
<p>The <strong>duties of a medical doctor</strong> include consulting with patients and determining skin ailments, prescribing medication, undertaking skin therapy treatment, or performing non-intrusive surgery. </p><p><strong>Your tasks will be : </strong></p><ul><li><p>Assist in Medical and dermatological treatments</p></li><li><p>Perform customer service and sales duties</p></li><li><p>Complete training will be offered to the candidate.</p></li></ul><p></p><p><strong>Requirements</strong></p><ul><li><p>Experience is a MUST!</p></li><li><p>Pharmacy/ Physical Therapy/</p></li><li><p><strong>People skills:</strong> An ability to interact well with others, and to be pleasant and friendly even under trying circumstances, can be invaluable.</p></li><li><p><strong>Think outside the box:</strong> Creativity and a willingness to adapt to new trends can be important.</p></li><li><p><strong>Be a good listener:</strong> People like to talk about themselves when they have time on their hands, such as when they're sitting still while you tend to them. You'll want to be able to provide appropriate feedback.</p></li><li><p><strong>Physical stamina: </strong>You'll spend a lot of time on your feet.</p></li><li><p><strong>Tidiness: </strong>This doesn't mean just your work station. Personal tidiness is very important as well. Remember, you're an example of your own work.</p></li></ul><p></p>
<p>Eva Cosmetics is currently hiring a <strong>Filling & Packaging Senior Specialist</strong> to join our Manufacturing team.</p><p>We are looking for a motivated professional who can lead filling and packaging operations, ensure high-quality production, and support our commitment to efficiency, safety, and continuous improvement across our production lines.</p><p> </p><p>Key Responsibilities</p><p>• Supervise the full filling and packaging process from work order release to final product delivery and closure.</p><p>• Ensure availability, accuracy, and readiness of all production materials, documentation, and approved packaging equipment prior to operation.</p><p>• Ensure strict compliance with GMP, GDP, ISO standards, Line Clearance requirements, and quality procedures throughout all production stages.</p><p>• Monitor production performance to achieve planned quantities with high quality while minimizing losses, deviations, and downtime.</p><p>• Lead, train, and evaluate filling and packaging operators, ensuring adherence to PPE, safety rules, and standard operating procedures.</p><p>• Prepare and submit production reports, update production systems, and coordinate with Engineering and Quality teams to resolve operational issues.</p><p><strong>Requirements</strong></p><ul><li><p>Bachelor’s Degree in Pharmacy, Agriculture or Science</p></li><li><p>Min. 2 years of related experience in Cosmetics or Pharmaceuticals Industry</p></li><li><p>Strong Knowledge of</p></li><li><p>Good English Language</p></li></ul><p></p>
<ul><li><p>Responsible for preparation of Registration dossiers of all new products and Re-registered products.</p></li><li><p>Submitting variations of existing products.</p></li><li><p>Responsible for preparation and submission of Analytical dossiers to NODCAR ( National Organization for Drug Control and Research ).</p></li><li><p>Follow up submission and any supporting documents along with registration lead time.</p></li><li><p>Support logistic team with all references, legalized certificates and material needed for regular analysis and release.</p></li><li><p>Prepare analytical files to be submitted to different authorized labs</p></li><li><p>Follow up analysis and supply all needed requirements to get release certificates f samples.</p></li><li><p>Ensures confidentiality in respect of registration files contents.</p></li><li><p>Completing all registration requirements for all shipments at EDA.</p></li><li><p>Responsible for obtaining Ministry of Health importation approvals, inspection & release.</p></li></ul><p></p><p><strong>Requirements</strong></p><ul><li><p>Bachelor’s degree in Science, pharmacy or vet medicine.</p></li><li><p>Knowledge of EDA regulatory affairs is a must.</p></li><li><p>Hands-on experience in medical devices registration is a must</p></li><li><p>Experience mainly in sterile medical devices regulatory and submissions in CAPA, NODCAR.</p></li><li><p>Good knowledge of preparation of registration files.</p></li><li><p>Excellent command of English and Arabic</p></li><li><p>1-3 years of experience.</p></li></ul><p></p>
<p>To meet the key performance indicators for executing the strategic directions and Goals by promoting and provide the access of our products to the healthcare professionals in reference to the company guidelines and policies.</p><p><strong>Desired Candidate Profile</strong></p><p>Bachelors degree of pharmacy. Experience in Neurology is essential, and experience in Multiple Sclerosis is a definite plus. Considerable proven commercial experience and successful track records of product enlisting & achievements for at least two year in the pharmaceutical industry. Demonstrate strong selling skills & possess flexible interpersonal skills that tends to collaborate to achieve the goals. Excellent negotiation skills. Valid Driving License. Good command of English language written/Spoken. Good command of computer & Microsoft office skills. Strong commitment to timelines and task achievements. Problem solving skills. Able to analyze situation & identify rising issues, seek solutions, and provide options for decision making. Identify opportunities and challenges and can communicate it effectively to management. Demonstrate the good values of integrity, respect, accountability, excellence, ownership & teamwork. Tendency to exert extra miles efforts in the territory to achieve the territory goals.</p>
<ul><li><p>Develop and execute the business unit strategy in line with the company's vision and objectives.</p></li><li><p>Achieve sales, market share, and profitability targets while ensuring sustainable business growth.</p></li><li><p>Lead, inspire, and develop high-performing Sales, Marketing, and cross-functional teams.</p></li><li><p>Analyze market trends, customer insights, and competitor activities to identify new business opportunities.</p></li><li><p>Build and maintain strong relationships with key opinion leaders (KOLs), customers, and strategic partners.</p></li><li><p>Develop annual business plans, sales forecasts, and budgets, while monitoring business performance through KPIs.</p></li><li><p>Collaborate closely with Medical, Regulatory, Supply Chain, and Finance teams to ensure successful product lifecycle management.</p></li><li><p>Ensure full compliance with company policies and pharmaceutical industry standards.</p></li></ul><p></p><p><strong>Requirements</strong></p><ul><li><p><strong>Bachelor’s degree in veterinary medicine, Science, or Pharmacy.</strong></p></li><li><p><strong>MBA is a strong advantage.</strong></p></li><li><p><strong>Minimum 8–10 years of experience</strong> in the pharmaceutical industry.</p></li><li><p><strong>At least 3 years of experience</strong> as a Business Unit Manager.</p></li><li><p>Proven track record of achieving business growth and exceeding commercial targets.</p></li><li><p>Strong strategic thinking, leadership, coaching, and decision-making skills.</p></li><li><p>Excellent communication, negotiation, and presentation skills.</p></li><li><p>Strong analytical mindset with outstanding business acumen.</p></li><li><p>Excellent command of English.</p></li></ul><p></p>
<p><b>About the Role</b></p><p>Key Responsibilities</p><p><br></p><p>Perform raw material testing and analysis using chromatography and related laboratory techniques.</p><p>Support compliant material release decisions to ensure production readiness and uninterrupted supply.</p><p>Maintain accurate documentation and strong data integrity across testing and quality records.</p><p>Ensure full compliance with Good Manufacturing Practices and site quality standards.</p><p>Support investigations and quality issue resolution in a high-pressure manufacturing environment.</p><p>Collaborate with production, procurement, and suppliers to prevent delays and resolve risks.</p><p>Contribute technical expertise to inspection readiness and continuous improvement initiatives.</p><p>Essential Requirements</p><p><br></p><p>Bachelor’s degree in Pharmacy or a related scientific field.</p><p>At least two years of experience in pharmaceutical quality control.</p><p>Hands-on experience in raw material testing, including chromatography-based analysis.</p><p>Strong knowledge of Good Manufacturing Practices and quality compliance requirements.</p><p>High attention to data integrity, documentation accuracy, and reliable execution.</p><p>Ability to manage complexity, solve problems quickly, and collaborate across teams.</p><p>Desirable Requirements</p><p><br></p><p>Experience in environmental monitoring</p><p>Exposure to quality control, analytical science and technology, or quality assurance environments.</p><p><strong>Desired Candidate Profile</strong></p><ul><li><br></li></ul>