Medical Representative Jobs in Saudi

Major Responsibilities Ensures through his action, either directly or indirectly, that a superior quality of medical treatment, compassion and understanding is given to every patient served at the Hospital and Clinics Plan, develop and maintain a system of Medical Report to attain the hospital goals and meet standards of CBAI I l & JCIA. Prepares technical reports reflecting the volume of work, procedures utilized and Medical Reports services: coordinate the preparation of reports and analyses setting forth progress. Adverse trends and appropriate recommendations or conclusions. Implements policies and procedures for processing/handling medical Report & reports (OP & Il)). Release of patient information. Incomplete medical Reports, and diagnostic data services (JCIA& CBAIII standard). Maintain sufficient inventory of materials and equipment for performance of duties and maintain standard Medical Report Department equipment with budgetary guidelines. Assure implementing Quality Assurance and Safety to comply with internal and external regulations. Train. Supervise and evaluate the performance of Medical Report Technicians, develop work performance standards. Schedule/assigns work and priorities and provide technical expertise as needed or requested. Organization and operation of Medical Reports services (OP & IP) in relation to the standards and in relation to new technology, e.g. computers, etc. and make appropriate revisions. Provides for a staff education and development program for new hire orientation, teaching, new procedures and techniques. Upgrading skills. Approves or recommends annual leave, educational leave, and training assignments. Taking an active role in helping the medical staff comply with the JCIA & CBAHI requirements for medical Report review.<br>Supplying data and assisting physicians in conducting research studies. Recommends employment promotion and release of personnel. Interfaces with the other departments to coordinate and resolve problems. Submits monthly reports to Hospital Administration and any additional reports as required. Submits Health Care Statistics to Manager Health Information Management (OP &IP) monthly. Quarterly. Half yearlong and annually. Maintain Medical Report code of ethics Performs applicable tasks and duties assigned within the realm of the employee is knows ledge. Skills and duties.<br>Reporting to• Director of Health Information Management<br>Supervises• Assistants.• Clerks.• Encoders.• Orderlies.<br>Experience:Required(5) years’ experience in a supervisor post in 350 beds hospital.<br>Competencies:Fluency in verbal and written English. Must possess complete familiarity with required medical Report documentation, Medical Terminology, Anatomy, Pathology and Health care statistics. Competent knows ledge and understanding of current medical records functions guidelines and principles.• Ability to understand diverse documentation style and read various diagnostic reports contained in the Medical Report. Ability to operate computerized patient information system and the personal Computer. Exhibits professionalism and excellent interpersonal communication skills

<div dir="rtl"><h3 >نبذة عن الوظيفة</h3> <p >تبحث شركة دار المعدات الطبيه والعلميه عن <strong >فني أجهزة طبية</strong> للانضمام إلى فريقها في منطقة عسير. يركز هذا الدور على متابعة تركيب وتشغيل وصيانة الأجهزة الطبية، بما في ذلك الصيانة العلاجية والوقائية، لضمان عملها بكفاءة وفقاً لتعليمات الشركات المصنعة. الوظيفة بدوام كامل وتتطلب خبرة تتراوح من 0 إلى 1 سنة.</p> <h3 >المهام والمسؤوليات الرئيسية</h3> <ul > <li >تتبع مخططات تركيب الأجهزة الطبية المتنوعة مثل أجهزة غسل الكلى، وأجهزة دعم القلب والتنفس والرئة، وأجهزة التصوير والتخطيط الطبي وغيرها.</li> <li >تحديد مواقع تركيب الأجهزة الطبية ومتابعة إجراءات التركيب.</li> <li >إعداد قوائم بقطع الغيار الاحتياطية اللازمة.</li> <li >متابعة إجراءات التشغيل التجريبي للأجهزة الطبية والتحقق من تشغيلها بحسب أدلة التشغيل.</li> <li >تدريب مستخدمي الأجهزة الطبية على إجراءات التشغيل السليم والضبط.</li> <li >تتبع مخططات الدارات الإلكترونية للأجهزة الطبية وتشخيص أعطالها باستخدام أجهزة الفحص والقياس.</li> <li >تنفيذ إجراءات الإصلاح والضبط.</li> <li >تنفيذ برامج الصيانة الوقائية للأجهزة الطبية بحسب تعليمات الشركة الصانعة.</li> <li >إعداد تقارير العمل وتقديمها وتوثيقها وحفظها.</li> </ul> <h3 >الخبرات المطلوبة</h3> <ul > <li >خبرة عملية تتراوح من <strong >0 إلى 1 سنة</strong> في مجال صيانة الأجهزة الطبية أو مجال تقني ذي صلة.</li> </ul> <h3 >المهارات والمتطلبات الأساسية</h3> <ul > <li >القدرة على قراءة وتتبع المخططات الفنية والكهربائية والإلكترونية للأجهزة الطبية.</li> <li >مهارة في استخدام أجهزة الفحص والقياس لتشخيص الأعطال.</li> <li >الالتزام بتعليمات الشركات المصنعة وإجراءات الصيانة الوقائية.</li> <li >مهارات جيدة في إعداد التقارير الفنية وتوثيق العمل.</li> </ul> <h3 >تفاصيل العمل</h3> <p >هذه الوظيفة بدوام كامل ومقرها في منطقة <strong >عسير</strong>. سيعمل الفني ضمن فريق متخصص لضمان الأداء الأمثل للأجهزة الطبية في المنشآت الصحية.</p> <h3 >التقديم</h3> <p >ندعو المهتمين الذين يستوفون المتطلبات المذكورة للتقديم لهذه الفرصة ضمن شركة دار المعدات الطبيه والعلميه.</p></div>

<div dir="rtl"><h3 >نبذة عن الدور</h3> <p >تبحث شركة دار المعدات الطبيه والعلميه عن <strong >فني أجهزة طبية</strong> للانضمام إلى فريقها في منطقتي الرياض والخرج. يمثل هذا الدور فرصة للمرشحين ذوي الخبرة التي تتراوح بين 0-1 سنة للعمل بدوام كامل في مجال حيوي يخدم القطاع الطبي.</p> <h3 >الغرض من الوظيفة</h3> <p >يتولى شاغل هذه الوظيفة مسؤولية متابعة جميع مراحل تركيب وتشغيل الأجهزة الطبية المتنوعة. كما يشمل الدور تنفيذ إجراءات الصيانة العلاجية وتطبيق برامج الصيانة الوقائية بدقة، وذلك لضمان الأداء الأمثل للأجهزة وفقاً للمواصفات وتعليمات الشركات المصنعة.</p> <h3 >المهام والمسؤوليات الرئيسية</h3> <ul > <li >تتبع مخططات تركيب الأجهزة الطبية مثل أجهزة غسل الكلى، وأجهزة دعم القلب والتنفس والرئة، وأجهزة التصوير والتخطيط الطبي، وغيرها.</li> <li >تحديد مواقع تركيب الأجهزة الطبية ومتابعة إجراءات التركيب لضمان الامتثال للمعايير.</li> <li >إعداد قوائم تفصيلية بقطع الغيار الاحتياطية اللازمة للأجهزة.</li> <li >متابعة إجراءات التشغيل التجريبي للأجهزة الطبية، وضمان تشغيلها الفعلي وفقاً لأدلة التشغيل المعتمدة.</li> <li >تدريب مستخدمي الأجهزة الطبية على إجراءات التشغيل السليم والضبط الصحيح.</li> <li >تتبع مخططات الدارات الإلكترونية للأجهزة الطبية وتشخيص الأعطال باستخدام أجهزة الفحص والقياس المتخصصة.</li> <li >تنفيذ إجراءات الإصلاح والضبط اللازمة للأجهزة المعطلة.</li> <li >تطبيق برامج الصيانة الوقائية للأجهزة الطبية بحسب تعليمات الشركة الصانعة لضمان استمرارية الأداء.</li> <li >إعداد وتقديم وتوثيق وحفظ تقارير العمل الدورية.</li> </ul> <h3 >المتطلبات والمؤهلات</h3> <ul > <li >خبرة عملية تتراوح بين <strong >0 إلى 1 سنة</strong> في مجال صيانة وتركيب الأجهزة الطبية.</li> </ul> <h3 >تفاصيل العمل والراتب</h3> <p >تُقدم شركة دار المعدات الطبيه والعلميه راتباً شهرياً يتراوح بين <strong >5900 إلى 6000 ريال سعودي</strong> لهذا الدور. الوظيفة بدوام كامل، وتقع في مدينتي الرياض والخرج، مما يوفر بيئة عمل مستقرة ضمن فريق متخصص.</p> <h3 >ختاماً</h3> <p >تلتزم شركة دار المعدات الطبيه والعلميه بتوفير بيئة عمل داعمة تساهم في تطوير الكفاءات الفنية في مجال الأجهزة الطبية.</p></div>

Job Summary The Medical Director is responsible for providing clinical leadership and oversight of medical services across the hospital. The role ensures high standards of patient care, clinical governance, physician performance, patient safety, and regulatory compliance while supporting the hospital’s strategic and operational objectives.<br>Key Responsibilities Provide clinical leadership and oversee the quality and performance of medical services across the hospital Lead medical staff governance, physician performance, credentialing, and clinical quality improvement activities Monitor clinical outcomes, patient safety indicators, and adherence to evidence-based clinical standards Collaborate with hospital leadership, department heads, nursing, and other teams to improve clinical and operational performance Ensure medical services comply with hospital policies, accreditation standards, ethical requirements, and applicable healthcare regulations<br>Qualifications Medical degree (MBBS, MD, or equivalent) from a recognized institution Valid SCFHS professional classification and registration Minimum 10 years of clinical experience, including medical leadership or management responsibilities Strong experience in clinical governance, quality improvement, patient safety, and physician management Healthcare or hospital leadership experience is required

Modern Methods Center is seeking an experienced Medical Director to join our team in Dammam, Saudi Arabia. Requirements:Minimum of 5 years of professional experience in the medical field. Previous experience in medical management or clinical supervision. Strong leadership, organizational, and communication skills. Good knowledge of healthcare regulations and standards in Saudi Arabia. Valid professional classification and license from the Saudi Commission for Health Specialties (SCFHS). Fluency in Arabic and English. Key Responsibilities:Oversee medical operations and clinical services within the center. Supervise and evaluate the performance of the medical team. Ensure compliance with clinical policies, quality standards, and patient safety requirements. Coordinate between the medical team and management. Maintain compliance with applicable healthcare regulations and requirements. Location: Dammam, Saudi Arabia Employment Type: Full-time Experience Required: 5+ Years

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <br>Company Description<br><br><p><strong>About AbbVie</strong></p><br><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;www.abbvie.com. Follow @abbvie on&nbsp;LinkedIn,&nbsp;Facebook,&nbsp;Instagram,&nbsp;X&nbsp;and&nbsp;YouTube.</p><br><br>Job Description<br><br><p><strong>PRIMARY FUNCTION: </strong></p><br><p>Represent the affiliate’s medical/scientific voice of expertise for assigned product(s) and relevant therapeutic area(s). Provide medical / scientific expert advice / guidance to key customers for assigned product(s) and relevant therapeutic area(s), including scientific exchange and professional relationship development with External Experts (EEs). Provide medical / scientific input into Medical Affairs strategies for the affiliate medical department and commercial plans, as required, and medical / scientific support for medical department activities under the overall direction of the Affiliate Medical Director. Provide medical affairs support to cross-functional affiliate teams. Ensure that the medical affairs role is fully integrated to support the strategy and execution of affiliate business, while being functionally independent.</p><br><p><strong>RESPONSIBILITIES:</strong></p><br><ol><li>Being an active brand team member to support overall strategy and execution. Provide medical/scientific input into marketing strategy and key commercial initiatives, as required.</li><li>Develop and maintain in-depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/area literature.</li><li>Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e., pricing and reimbursement dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.).</li><li>Establish and maintain professional and credible relationships with External Experts (EEs) and academic centers; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion forums etc.</li><li>Deliver scientific presentations and medical education programs to healthcare professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate.</li><li>Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.)</li><li>Deliver training to sales forces and other departments; develop and update relevant training materials.</li><li>Clinical Research Activities:<ol><li>Design and implement clinical research projects within defined standards and budgets (e.g., Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies).</li><li>Provide the required oversight to manage review, approval and conduct of IIS studies.</li><li>Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g., review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys).</li></ol></li><li>Review and preparation of promotional / non-promotional material. Ensure the medical/scientific content is correct, balanced fair and fully compliant with AbbVie’s internal policies and guidelines and in accordance with local laws.</li><li>Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, AbbVie’s policies and procedures and accepted standards of best practice.</li><li>Provide input, as required, into the development of product or TA specific strategic medical affairs plans for the affiliate medical department and local commercial plans; collaborate and partner with local business partners to ensure that medical activities for assigned products / therapeutic areas are aligned with local business-related strategic plans.</li><li>Ensure adherence to all applicable national laws and regulations, guidelines, codes of conduct, AbbVie standards, policies, and procedures.</li><li>Operate as a scientific interface and resource to HCPs/Customer(s), Health Care Institutions, External Experts, and professional associations regarding assigned AbbVie Products or Products in Development.</li><li>Provide specialist medical/scientific strategic input and operational support of core activities such as local clinical research, HCP/Customer interactions, generation and communication of clinical and scientific data, educational initiatives, and patient safety for assigned products / therapeutic areas.</li></ol><p><strong>LOCATION: Riyadh</strong></p><br><p>This function is hybrid in nature. Typically, up to 50% of an individual’s time may be spent working in the field.</p><br><br>Qualifications<br><br><ul><li><p><strong>QUALIFICATIONS:</strong></p><br></li><li>Advanced degree (e.g. PharmD., PharmB., MD, PhD) in a relevant scientific discipline is preferred but candidates with an undergraduate degree in a relevant discipline and demonstrated experience will be considered</li><li>Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company.</li><li>Prior experience in Medical Affairs is a must with a minimum of 2 years.</li><li>Prior experience in solid tumors and/or companion diagnostics, or in specialty therapeutic areas, is required.</li><li>Experience in evidence generation, including Real-World Evidence (RWE), non-interventional studies, registries and/or investigator-initiated studies.</li><li>Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research.</li><li>Ability to comprehensively learn about new subject areas and environments.</li><li>Excellent written and spoken communication and presentation skills, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians, and other healthcare decision makers.</li><li>An excellent understanding of written and oral English is mandatory.</li><li>Collaborative, team-oriented approach, able to develop and support relationships across an organization as well as with key external stakeholders and the healthcare community at large.</li><li>Experience being an active contributor to cross-functional teams and/or working in matrix organizations will be an advantage. </li><li>Works independently: limited guidance/oversight. Works broadly across functions to facilitate and support the affiliate’s medical and clinical activities as necessary.</li><li>Sound judgment, strong planning and organizational skills, and the ability to get things done. Demonstrated strong sense of urgency.</li><li>High customer orientation and high digital savviness skills.</li><li>Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity</li><li>Ability to travel regularly (approximately 50%)</li></ul><br>Additional Information<br><br><p><strong>INTERNAL / EXTERNAL CONTACTS AND INTERACTIONS:</strong></p><br><ul><li>In-Field/Brand Team members (as applicable)</li><li>Affiliate R&amp;D personnel: Medical Director, Medical operation and Evidence Generation Specialist, Medical Managers/Advisors; Medical Information team / specialists; affiliate pharmacovigilance / drug safety personnel (as applicable)</li><li>Marketing and Sales of assigned product and therapeutic area; Market access teams; Affiliate Brand teams.</li><li>Affiliate Government Affairs; Affiliate Public Affairs; Regulatory Affairs; Legal; OEC.</li><li>Area and HQ based Therapeutic Area medical affairs teams.</li><li>Area Medical Affairs teams</li><li>Medical Directors and Clinical Teams within Clinical Development Operations and Global Medical Affairs.</li><li>Healthcare personnel (including physicians, nurses, pharmacists).</li><li>Participating Research Investigators; thought leaders/external experts.</li><li>Institutions and Scientific or Medical Societies.</li><li>Hospitals, other healthcare providers, payers, and Local Regulatory Authorities.</li></ul><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.&nbsp;</p><br><p>US &amp; Puerto Rico only - to learn more, visit&nbsp;https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</p><br><p>US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><br><p>https://www.abbvie.com/join-us/reasonable-accommodations.html</p><br> </div><h2 data-automation-id="subHeaderPreferredCandidate" class="h5"> Preferred candidate </h2> <div class="row is-m v-align-top t-small bg-mute"> <div class="col is-3 p5" data-automation-id="label_Years_of_experience"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> 1+ years </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Nationality"> <b>Nationality</b> </div> <div class="col is-9 p5" data-automation-id="data_Nationality"> Saudi Arabia </div> </div> <div class="row is-m v-align-top t-small bg-mute"> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<div dir="rtl"><h3 >نبذة عن الدور</h3> <p >تبحث شركة أزير التجارية عن <strong >فني أجهزة طبية</strong> للانضمام إلى فريقها في مدينة الرياض. يركز هذا الدور على ضمان الأداء السليم والفعال للأجهزة الطبية من خلال الإشراف على التركيب والتشغيل، وتنفيذ برامج الصيانة الوقائية والعلاجية وفقًا لمعايير الشركة المصنعة.</p> <h3 >الغرض من الوظيفة</h3> <p >يتولى شاغل هذه الوظيفة مسؤولية متابعة جميع مراحل دورة حياة الأجهزة الطبية، بدءًا من التركيب والتشغيل الأولي، مروراً بتدريب المستخدمين، وصولاً إلى تنفيذ إجراءات الصيانة الدورية والعلاجية. يهدف الدور إلى الحفاظ على جاهزية الأجهزة الطبية وكفاءتها التشغيلية لضمان استمرارية العمليات.</p> <h3 >المهام والمسؤوليات الرئيسية</h3> <ul > <li >تتبع مخططات تركيب الأجهزة الطبية، مثل أجهزة التنفس والرئة والتخطيط الطبي وغيرها، وتحديد مواقع التركيب المناسبة.</li> <li >متابعة إجراءات تركيب الأجهزة الطبية وإعداد قوائم بقطع الغيار الاحتياطية اللازمة لضمان توفرها.</li> <li >الإشراف على إجراءات التشغيل التجريبي للأجهزة الطبية ومتابعة تشغيلها الفعلي وفقًا لأدلة التشغيل المعتمدة.</li> <li >تدريب مستخدمي الأجهزة الطبية على إجراءات التشغيل السليم والضبط الصحيح لضمان الاستخدام الأمثل.</li> <li >تتبع مخططات الدارات الإلكترونية للأجهزة الطبية وتشخيص الأعطال باستخدام أجهزة الفحص والقياس المتخصصة.</li> <li >تنفيذ إجراءات الإصلاح والضبط اللازمة للأجهزة الطبية المعطلة.</li> <li >تنفيذ برامج الصيانة الوقائية للأجهزة الطبية بحسب تعليمات الشركة الصانعة لضمان استمرارية الأداء.</li> <li >إعداد وتقديم وتوثيق وحفظ تقارير العمل المتعلقة بجميع المهام المنجزة.</li> </ul> <h3 >المؤهلات والخبرات المطلوبة</h3> <ul > <li >خبرة تتراوح من <strong >0 إلى 1 سنة</strong> في مجال صيانة وتركيب الأجهزة الطبية.</li> <li >القدرة على قراءة وتتبع المخططات الفنية والكهربائية للأجهزة الطبية.</li> <li >مهارات جيدة في استخدام أجهزة الفحص والقياس لتشخيص الأعطال.</li> </ul> <h3 >بيئة العمل ونوع الدوام</h3> <p >تتطلب هذه الوظيفة العمل بدوام كامل في مدينة الرياض. سيعمل الفني ضمن فريق متخصص لتقديم الدعم الفني للأجهزة الطبية.</p> <h3 >التقديم للوظيفة</h3> <p >ندعو المهتمين الذين يستوفون المتطلبات المذكورة أعلاه للتقدم لهذه الفرصة في شركة أزير التجارية.</p></div>

<div dir="rtl"><h3 >نبذة عن الدور</h3> <p >تبحث شركة سمايا الحديثة للخدمات الطبية عن <strong >مهندس أجهزة طبية</strong> للانضمام إلى فريقها في جدة، مكة المكرمة. يركز هذا الدور بدوام كامل على تركيب وصيانة وتشخيص الأجهزة الطبية، بالإضافة إلى إعداد برامج الصيانة الوقائية.</p> <h3 >المهام والمسؤوليات الرئيسية</h3> <ul > <li >إعداد خطط وبرامج تركيب الأجهزة الطبية، مثل أجهزة التصوير الإشعاعي والموجي وأجهزة التشخيص والمعالجة.</li> <li >تدريب المستخدمين على تشغيل الأجهزة الطبية بشكل فعال وآمن.</li> <li >تشخيص أعطال الأجهزة الطبية ومتابعة إجراءات الإصلاح والصيانة اللازمة.</li> <li >إجراء الفحوصات الضرورية للتأكد من دقة أداء الأجهزة بعد الصيانة أو الإصلاح.</li> <li >إعداد برامج الصيانة الوقائية للأجهزة الطبية وفقاً لتعليمات الشركة المصنعة ومتابعة تنفيذها.</li> <li >تطوير أساليب وإجراءات العمل ومواكبة التطورات التقنية في مجال الأجهزة الطبية.</li> <li >إعداد الوثائق والتقارير المتخصصة بالأعمال والمشروعات الهندسية، وتوضيح نسب تقدمها وحفظها في قاعدة البيانات المعتمدة.</li> </ul> <h3 >المؤهلات والخبرة</h3> <ul > <li >خبرة تتراوح من 0 إلى 1 سنة في مجال هندسة الأجهزة الطبية.</li> <li >القدرة على إعداد خطط وبرامج تركيب الأجهزة الطبية.</li> <li >مهارات تشخيص الأعطال ومعالجتها بكفاءة.</li> <li >القدرة على إعداد ومتابعة برامج الصيانة الوقائية.</li> </ul> <h3 >بيئة العمل</h3> <p >هذا الدور هو وظيفة بدوام كامل ضمن فريق شركة سمايا الحديثة للخدمات الطبية في جدة، مكة المكرمة.</p> <h3 >التقديم</h3> <p >للمهتمين بالانضمام إلى فريقنا، يرجى التقديم لهذه الفرصة في مجال هندسة الأجهزة الطبية.</p></div>

Kinetic is working with a leading Pharmaceutical company who are hiring a Medical Advisor - Oncology to be based in Riyadh.<br>***Please take the time to read the job description, you must meet all the criteria set out below for your application to be considered. We do check all applications and suitable candidates will be contacted within 5 working days. If you are not contacted by us within that time, please consider your application unsuccessful on this occasion.***<br>Key aspects of the role include:Develop and maintain scientific and medical expertise. Facilitate scientific engagement, scientific exchange, and medical information. Provide clinical presentations and respond to medical requests. Providing medical support for patients and formulary access products following global and local policies and procedures. Supporting the development, implementation, and completion of medical activities. Build good relationships with Key Opinion Leaders, healthcare professionals, and organizations. To support & back up the Marketing, Sales & Regulatory departments in scientific and medical issues to achieve the company’s objectives. Serves as a medical expert for internal medical and sales training. Support clinical research and IIS (Investigator Initiated Studies) and observational studies following guidelines & company-relevant SOPs. Attending relevant scientific meetings and conferences and supporting the development of summaries of key data, presentations, or symposiums.<br>To be successful you will need to meet the following:Due to Saudization, only Saudi nationals will be considered for this position. Medical degree (MD), Pharm D, or relevant life-science qualification. Minimum 3 years of experience in Medical Affairs within the pharmaceuticals industry. Experience in Oncology Medical Affairs is a must Strong understanding of oncology therapeutic areas and the Saudi healthcare landscape. Excellent scientific communication and presentation skills. Ability to engage effectively with external experts and internal stakeholders.<br>Hiring? If you need help filling a similar position in your company, please contact us on +971(0)4 433 4579 or click here.<br>***We check all applications and suitable candidates will be contacted within 5 working days. If you are not contacted by us within that time, please consider your application unsuccessful on this occasion.***

<h2 class="h5">Job description</h2> <div class="t-break" data-jb-field="description"> <p><b>Job Description Summary</b></p><br><br>In line with overall product strategy, the Medical Manager is a customer-facing responsible for supporting the design, implementation and execution of Medical Affairs plans for assigned Therapy Area, providing scientific information, helping design &amp; organize clinical studies, build-ing educational dialogue with MEs and regulatory stakeholders<br><p><b>Job Description</b></p><br><br><p><span><span><b><span><br>Job Description</span></b></span></span></p><br><br><p><span><span><b><span>Key Responsibilities:</span></b></span></span></p><br><br><p><span><span><span>Respond to medical enquiries accurately, compliantly, and in a timely manner, including developing standard response documents where needed.</span></span></span></p><br><br><ul><li><span><span><span>Provide medical and scientific input into clinical trial and research activities, including study initiation and oversight within the therapy area.</span></span></span></li><li><span><span><span>Support local evidence-generation activities, including non-interventional studies and investigator-initiated trials.</span></span></span></li><li><span><span><span>Build scientific partnerships across the disease journey by engaging medical experts, supporting publications, and contributing to data generation initiatives.</span></span></span></li><li><span><span><span>Review and approve medical and promotional materials in line with local and global compliance requirements.</span></span></span></li><li><span><span><span>Share actionable medical insights with cross-functional stakeholders including Pharmacovigilance, Regulatory, Market Access, Quality, and Commercial teams.</span></span></span></li><li><span><span><span>Role involves 50% external stakeholder engagement and 50% office-based responsibilities.</span></span></span></li></ul><p><span><span><b><span>Essential Requirements:</span></b></span></span></p><br><br><ul><li><span><span><span>Degree in MD, PharmD or PhD</span></span></span></li><li><span><span><span>Minimum 2 years’ experience in Medical Affairs in pharmaceutical industry, specific experience in Neuroscience is a plus</span></span></span></li><li><span><span><span>Proven ability to build credible relationships with medical experts and key decision-makers.</span></span></span></li><li><span><span><span>Strong understanding of clinical research, evidence generation, and the evolving therapeutic landscape.</span></span></span></li><li><span><span><span>Experience translating scientific insights into meaningful cross-functional action.</span></span></span></li><li><span><span><span>Confidence using digital tools and data to support stakeholder engagement, insight gathering, and decision-making.</span></span></span></li><li><span><span><span>Excellent communication, presentation, and collaboration skills in a matrix environment.</span></span></span></li><li><span><span><span>Fluency in both Arabic and English languages</span></span></span></li></ul><br><br><p><b>Skills Desired</b></p><br><br>Clinical Research, Clinical Trials, Drug Development, Health Sciences, Immunology, Internal Medicine, Medical Information, Patient Care, Stakeholder Engagement<br> </div><h2 data-automation-id="subHeaderPreferredCandidate" class="h5"> Preferred candidate </h2> <div class="row is-m v-align-top t-small bg-mute"> <div class="col is-3 p5" data-automation-id="label_Years_of_experience"> <b>Years of experience</b> </div> <div class="col is-9 p5" data-automation-id="data_Years_of_experience"> 1+ years </div> </div> <div class="row is-m v-align-top t-small "> <div class="col is-3 p5" data-automation-id="label_Degree"> <b>Degree</b> </div> <div class="col is-9 p5" data-automation-id="data_Degree"> Bachelor's degree / higher diploma </div> </div>

<p><span >MD Degree Current, active medical license in: Canada, the United States, the UK, Western Europe, Australia or New Zealand Fellowship in Breast Cancer/Breast Malignancies National Board Subspecialty Certification in Oncology from the United States, Canada, the UK, Western Europe, Australia, or New Zealand Current, active medical license in: Canada, the United States, the UK, Western Europe, Australia or New Zealand Minimum 10 years of current post-specialty certification experience working as a Consultant in Medical Oncology, specializing in Breast Cancer in a tertiary-care, academic hospital in the United States, Canada, the UK, Western Europe, Australia, or New Zealand</span></p><p><strong>Desired Candidate Profile</strong></p><p><br></p>

<div dir="rtl"><h3 >نبذة عن الدور</h3> <p >يبحث مجمع داهم الطبي عن <strong >أخصائي مختبرات طبية</strong> للانضمام إلى فريقه في الهفوف، المنطقة الشرقية. يركز هذا الدور على ضمان دقة الفحوصات المخبرية وتوفير الدعم اللازم للعمليات التشخيصية، مع الالتزام بمعايير السلامة والجودة. تتطلب الوظيفة خبرة تتراوح من 0 إلى 1 سنة، وهي بدوام كامل.</p> <h3 >المهام والمسؤوليات الرئيسية</h3> <ul > <li >تحديد احتياجات المختبر من المواد الأولية اللازمة للفحوصات الطبية وتوفيرها، مع التأكد من سلامتها وتعقيمها ومراقبة فترة صلاحيتها.</li> <li >استلام عينات الفحص من المرضى وحفظها بالطرق السليمة، وإجراء التحاليل الكيميائية والفيزيائية والمجهرية لتحديد وجود السكر أو البروتين أو الجراثيم والطفيليات.</li> <li >دراسة نتائج الاختبار وإعداد التقارير المتعلقة بها بدقة واحترافية.</li> <li >تطوير أساليب وإجراءات العمل في المختبر ومواكبة التطورات الحديثة في أساليب التحاليل الطبية.</li> <li >إعداد الوثائق والتقارير الطبية المتعلقة بالتحاليل الطبية للمرضى وحفظها في قاعدة البيانات الخاصة بها، وفقاً للسياسات والإجراءات المنظمة.</li> <li >ضمان تطبيق مبادئ وقواعد السلامة العامة أثناء القيام بمختلف أعمال المختبرات الطبية للحفاظ على بيئة عمل آمنة.</li> </ul> <h3 >المؤهلات والخبرات المطلوبة</h3> <ul > <li >خبرة عملية تتراوح من <strong >0 إلى 1 سنة</strong> في مجال المختبرات الطبية.</li> <li >القدرة على تحديد احتياجات المختبر من المواد الطبية وإدارتها.</li> <li >مهارات ممتازة في إجراء التحاليل المخبرية المختلفة.</li> <li >القدرة على إعداد التقارير والوثائق الطبية بدقة.</li> </ul> <h3 >بيئة العمل</h3> <p >يعمل أخصائي المختبرات الطبية ضمن فريق مجمع داهم الطبي في الهفوف، المنطقة الشرقية. تتطلب الوظيفة الالتزام بالعمل بدوام كامل في بيئة مختبرية تتطلب الدقة والتركيز.</p> <h3 >فرصة العمل</h3> <p >هذه فرصة للانضمام إلى فريق طبي متخصص والمساهمة في تقديم خدمات رعاية صحية عالية الجودة. الراتب سيتم تحديده بناءً على الخبرة والمؤهلات.</p></div>

<h3 >About Dallah Healthcare and the Role</h3> <p >Dallah Healthcare is seeking a dedicated <strong >Medical Insurance Coordinator</strong> to join our team in a full-time capacity. This role is integral to supporting the Revenue Cycle management by providing essential medical administration and coordination services, ensuring efficient interaction with clients, medical staff, and insurance providers.</p> <h3 >Core Insurance Coordination Responsibilities</h3> <ul > <li >Participate in the creation and review of contractual agreements with clients.</li> <li >Coordinate effectively with medical staff regarding client contracts, requirements, and necessary forms.</li> <li >Liaise with insurance companies to address rejections and manage responses to ensure smooth processing.</li> </ul> <h3 >Revenue Cycle Support and Financial Settlement</h3> <ul > <li >Provide medical support to the approval section for various medical procedures and services.</li> <li >Offer medical support to the claims processing center to facilitate accurate and timely claim submissions.</li> <li >Assist the billing section with medical expertise to ensure correct invoicing.</li> <li >Manage reconciliation processes with insurance companies to achieve final settlements.</li> </ul> <h3 >Operational Compliance and Quality Improvement</h3> <ul > <li >Maintain full awareness of and actively implement departmental policies and procedures, alongside local and international standards.</li> <li >Contribute to indicator development and data collection to measure performance of departmental functions, processes, and outcomes.</li> <li >Conduct analysis and interpretation of collected data and information as required.</li> <li >Participate in hospital Safety Management and Risk Management Programs.</li> <li >Actively report incidents within the system and engage in incident review and root cause analysis when necessary.</li> <li >Perform additional duties within professional knowledge and skills as directed by the Revenue Cycle Director.</li> </ul> <h3 >Required Qualifications and Experience</h3> <ul > <li >A minimum of <strong >3 years of postgraduate experience</strong> in medical practice.</li> <li >A minimum of <strong >2 years of practical experience</strong> in medical administration.</li> <li >Must hold a valid license from the Saudi Ministry of Health.</li> </ul> <h3 >Application Process</h3> <p >Candidates who meet the above qualifications are encouraged to apply for this full-time position. Salary details will be discussed during the interview process.</p>

We are seeking a detail-oriented and organized Approval Coordinator to join our healthcare team. In this role, you will be responsible for managing and facilitating the medical insurance approval process for outpatients. You will act as the primary liaison between medical practitioners, patients, and insurance companies to ensure timely approvals for procedures, medications, and paramedical services, thereby ensuring a seamless patient experience.<br><br>Key Responsibilities<br>• Insurance Verification: Verify patients' insurance eligibility, benefits, and coverage limits before medical procedures or consultations.<br>• Pre-Authorization Requests: Prepare, submit, and track pre-authorization and medical approval requests to various insurance companies.<br>• Documentation Management: Review medical files, diagnoses, and doctors' recommendations to ensure all necessary documentation is accurate and complete before submission.<br>• Liaison &amp; Communication: Serve as the main point of contact between medical providers (doctors/nurses) and insurance companies to resolve any queries or rejections.<br>• Dispute &amp; Appeal Handling: Follow up on delayed or denied approvals, gathering additional medical justification from physicians to submit effective appeals.<br>• Patient Support: Guide patients through their insurance approval status, explaining coverage details, co-payments, or out-of-pocket expenses clearly and empathetically.<br>• Data Entry: Maintain accurate and up-to-date records of all approval statuses, codes (ICD-10 / CPT), and insurance communications in the clinic’s management system.<br><br>Requirements &amp; Qualifications<br>• Education: Bachelor’s degree or Diploma in Healthcare Administration, Nursing, Medical Coding, or a related field.<br>• Experience: Minimum of 1–3 years of experience as an Approval Coordinator or Insurance Officer within a hospital or medical center in Saudi Arabia.<br>• Insurance Knowledge: Deep understanding of the Saudi health insurance market, CCHI regulations, and major insurance provider portals (e.g., Bupa, Tawuniya, Medgulf).<br>• Medical Terminology: Strong familiarity with medical terminology, diagnostic codes (ICD), and procedure codes.<br>• Skills: Excellent communication and negotiation skills. High attention to detail with strong problem-solving abilities.<br>• Languages: Fluency in both English and Arabic (written and spoken) is required.

JOB PURPOSE : Coordinate and perform the implementation of SAICO medical approval operation services<br>KEY RESPONSIBILITIES : Conduct ongoing clinical evaluation of treatment plans and return‑to‑work plans in accordance with established medical standards and protocols. Process and manage all medical approval transactions per shift, ensuring adherence to approved policies and coverage guidelines. Ensure compliance with approval Turnaround Time (TAT) as follows: Out‑Patient (VVIP, VIP, A Classes): 0–10 minutes Out‑Patient (B, C, D Classes): 0–15 minutes In‑Patient (All Classes): Less than 60 minutes Review and respond to approval requests as per policy coverage, requesting additional medical information when required to support appropriate decision‑making. Coordinate with medical providers to ensure appropriate care delivery and suggest cost‑effective treatment alternatives when medically appropriate. Maintain effective communication with healthcare providers not covered by field doctors to ensure continuity and quality of care. Obtain and review medical records and supporting documentation from providers during initial contact, with appropriate follow‑up through written correspondence. Liaise with medical providers and injured parties in cases involving medical treatment to coordinate appropriate and timely medical care. Improve the quality, clarity, and medical justification of approval responses while maintaining cost effectiveness of medical services. Identify and refer suspicious or high‑risk cases to the Fraud, Waste, and Abuse (FWA) team in line with internal guidelines. Ensure accurate documentation of all case activities, including contacts, decisions, and outcomes, within the system; submit billing or activity reports when applicable and required by standards. Participate in Learning & Development activities and complete a minimum of 25 training hours to maintain clinical, operational, and insurance knowledge. <br>QUALIFICATIONS & EXPERIENCE:Minimum Qualifications: Medicine Bachelor’s degree (MBBS). Licensed by the Saudi Commission for Health Specialties (SCFHS). <br>Minimum Related Experience: 1-3 years’ experience in related field.

Kinetic is working with a leading Pharmaceutical company who are hiring a Medical Advisor - Oncology to be based in Riyadh.<br>***Please take the time to read the job description, you must meet all the criteria set out below for your application to be considered. We do check all applications and suitable candidates will be contacted within 5 working days. If you are not contacted by us within that time, please consider your application unsuccessful on this occasion.***<br>Key aspects of the role include:Develop and maintain scientific and medical expertise. Facilitate scientific engagement, scientific exchange, and medical information. Provide clinical presentations and respond to medical requests. Providing medical support for patients and formulary access products following global and local policies and procedures. Supporting the development, implementation, and completion of medical activities. Build good relationships with Key Opinion Leaders, healthcare professionals, and organizations. To support & back up the Marketing, Sales & Regulatory departments in scientific and medical issues to achieve the company’s objectives. Serves as a medical expert for internal medical and sales training. Support clinical research and IIS (Investigator Initiated Studies) and observational studies following guidelines & company-relevant SOPs. Attending relevant scientific meetings and conferences and supporting the development of summaries of key data, presentations, or symposiums.<br>To be successful you will need to meet the following:Due to Saudization, only Saudi nationals will be considered for this position. Medical degree (MD), Pharm D, or relevant life-science qualification. Minimum 3 years of experience in Medical Affairs within the pharmaceuticals industry. Experience in Oncology Medical Affairs is a must Strong understanding of oncology therapeutic areas and the Saudi healthcare landscape. Excellent scientific communication and presentation skills. Ability to engage effectively with external experts and internal stakeholders.<br>Hiring? If you need help filling a similar position in your company, please contact us on +971(0)4 433 4579 or click here.<br>***We check all applications and suitable candidates will be contacted within 5 working days. If you are not contacted by us within that time, please consider your application unsuccessful on this occasion.***

<h3 >About the Role</h3> <p >Novartis is seeking a <strong >Medical Manager</strong> to join their team. This full-time role is customer-facing and focuses on supporting the design, implementation, and execution of Medical Affairs plans for an assigned Therapy Area, aligning with the overall product strategy. The position requires 2-5 years of relevant experience.</p> <h3 >Role Context and Objectives</h3> <p >The Medical Manager provides scientific information, assists in designing and organizing clinical studies, and fosters educational dialogue with Medical Experts (MEs) and regulatory stakeholders. The role involves a balanced approach, with approximately <strong >50% external stakeholder engagement</strong> and <strong >50% office-based responsibilities</strong>.</p> <h3 >Key Responsibilities</h3> <ul > <li >Respond to medical enquiries accurately, compliantly, and in a timely manner, including developing standard response documents as needed.</li> <li >Provide medical and scientific input into clinical trial and research activities, including study initiation and oversight within the therapy area.</li> <li >Support local evidence-generation activities, such as non-interventional studies and investigator-initiated trials.</li> <li >Build scientific partnerships across the disease journey by engaging medical experts, supporting publications, and contributing to data generation initiatives.</li> <li >Review and approve medical and promotional materials in line with local and global compliance requirements.</li> <li >Share actionable medical insights with cross-functional stakeholders, including Pharmacovigilance, Regulatory, Market Access, Quality, and Commercial teams.</li> </ul> <h3 >Required Qualifications and Experience</h3> <ul > <li >Proven ability to build credible relationships with medical experts and key decision-makers.</li> <li >Strong understanding of clinical research, evidence generation, and the evolving therapeutic landscape.</li> <li >Experience translating scientific insights into meaningful cross-functional action.</li> <li >Confidence using digital tools and data to support stakeholder engagement, insight gathering, and decision-making.</li> <li >Excellent communication, presentation, and collaboration skills in a matrix environment.</li> </ul> <h3 >Work Type</h3> <p >This is a full-time position.</p> <h3 >Application Information</h3> <p >Salary for this position will be disclosed during the recruitment process.</p>

<h3 >About the Medical Manager Role at Novartis Pharma Schweiz</h3> <p >Novartis Pharma Schweiz is seeking a Medical Manager to join their team in Saudi Arabia. This is a full-time position that requires 2-5 years of relevant experience. The Medical Manager will play a key role in providing medical and scientific expertise within the therapy area, engaging with external stakeholders, and ensuring compliance with regulatory standards.</p> <h3 >Core Responsibilities</h3> <ul > <li >Respond to medical enquiries accurately, compliantly, and in a timely manner, including the development of standard response documents as needed.</li> <li >Provide medical and scientific input into clinical trial and research activities, encompassing study initiation and oversight within the designated therapy area.</li> <li >Support local evidence-generation activities, which include non-interventional studies and investigator-initiated trials.</li> <li >Build scientific partnerships across the disease journey by engaging medical experts, supporting publications, and contributing to data generation initiatives.</li> <li >Review and approve medical and promotional materials in alignment with local and global compliance requirements.</li> <li >Share actionable medical insights with cross-functional stakeholders, including Pharmacovigilance, Regulatory, Market Access, Quality, and Commercial teams.</li> </ul> <h3 >Experience and Engagement</h3> <p >Candidates for this role should possess 2-5 years of experience. The position involves a balanced approach to work, with approximately <strong >50% external stakeholder engagement</strong> and <strong >50% office-based responsibilities</strong>. This structure ensures a comprehensive involvement in both external scientific collaboration and internal operational duties.</p> <h3 >Work Type and Location</h3> <p >This is a <strong >full-time</strong> position based in <strong >Saudi Arabia</strong>. The role requires a consistent presence to manage both internal tasks and external engagements effectively within the region.</p>

<div dir="rtl"><h3 >نبذة عن الدور</h3> <p >تبحث شركة المعمر لانظمة المعلومات عن <strong >فني أجهزة طبية</strong> للانضمام إلى فريقها في مدينة حائل. يركز هذا الدور بدوام كامل على متابعة تركيب وتشغيل الأجهزة الطبية، بالإضافة إلى تنفيذ برامج الصيانة الوقائية والعلاجية لضمان كفاءة عملها وفقاً لتعليمات الشركات المصنعة. يتطلب الدور خبرة تتراوح بين 0-1 سنة. الراتب لهذه الوظيفة لم يتم الإفصاح عنه.</p> <h3 >المهام والمسؤوليات</h3> <ul > <li >تتبع مخططات تركيب الأجهزة الطبية المتنوعة، مثل أجهزة غسل الكلى، وأجهزة دعم القلب والتنفس والرئة، وأجهزة التصوير والتخطيط الطبي، وغيرها.</li> <li >تحديد المواقع المناسبة لتركيب الأجهزة الطبية ومتابعة إجراءات التركيب.</li> <li >إعداد قوائم مفصلة بقطع الغيار الاحتياطية الضرورية للأجهزة.</li> <li >متابعة إجراءات التشغيل التجريبي للأجهزة الطبية والتأكد من تشغيلها وفقاً لأدلة التشغيل المعتمدة.</li> <li >تدريب مستخدمي الأجهزة الطبية على إجراءات التشغيل السليم والضبط الصحيح.</li> <li >تتبع مخططات الدارات الإلكترونية للأجهزة الطبية وتشخيص أعطالها باستخدام أجهزة الفحص والقياس المتخصصة.</li> <li >تنفيذ إجراءات الإصلاح والضبط اللازمة للأجهزة الطبية المعطلة.</li> <li >تنفيذ برامج الصيانة الوقائية للأجهزة الطبية بدقة، بما يتماشى مع تعليمات الشركة الصانعة.</li> <li >إعداد وتقديم وتوثيق وحفظ تقارير العمل الدورية.</li> </ul> <h3 >المؤهلات والخبرات المطلوبة</h3> <ul > <li >خبرة عملية تتراوح بين <strong >0 إلى 1 سنة</strong> في مجال صيانة وتركيب الأجهزة الطبية أو مجال ذي صلة.</li> <li >القدرة على قراءة وتتبع المخططات الفنية والكهربائية للأجهزة الطبية.</li> <li >مهارات جيدة في استخدام أجهزة الفحص والقياس لتشخيص الأعطال.</li> <li >القدرة على تدريب المستخدمين وتقديم الدعم الفني.</li> </ul> <h3 >بيئة العمل</h3> <p >يعمل شاغل هذه الوظيفة بدوام كامل ضمن فريق شركة المعمر لانظمة المعلومات في مدينة <strong >حائل</strong>، المملكة العربية السعودية.</p> <h3 >التقديم</h3> <p >ندعو المهتمين الذين يستوفون المتطلبات المذكورة للتقديم على هذه الفرصة.</p></div>

<div dir="rtl"><h3 >نبذة عن الدور</h3> <p >تبحث شركة المعمر لانظمة المعلومات عن <strong >مهندس أجهزة طبية</strong> للانضمام إلى فريقها في مدينة حائل. يركز هذا الدور بدوام كامل على الإشراف الفني الشامل على الأجهزة الطبية، بدءاً من مراحل التركيب والتشغيل وصولاً إلى الصيانة الدورية وتشخيص الأعطال. يتطلب الدور خبرة عملية تتراوح بين 0-1 سنة في المجال.</p> <h3 >المهام والمسؤوليات الأساسية</h3> <p >يتولى مهندس الأجهزة الطبية مجموعة من المهام الأساسية لضمان كفاءة وسلامة تشغيل الأجهزة الطبية، وتشمل ما يلي:</p> <ul > <li >إعداد خطط وبرامج تركيب الأجهزة الطبية المتنوعة، مثل أجهزة التصوير الإشعاعي والموجي، وأجهزة التشخيص والمعالجة.</li> <li >تدريب المستخدمين على التشغيل السليم والآمن للأجهزة الطبية المركبة.</li> <li >تشخيص الأعطال الفنية في الأجهزة الطبية ومتابعة إجراءات الإصلاح والصيانة اللازمة.</li> <li >إجراء الفحوص الدورية اللازمة للتأكد من دقة أداء الأجهزة الطبية بعد الصيانة أو التركيب.</li> </ul> <h3 >الصيانة والتطوير</h3> <ul > <li >إعداد برامج الصيانة الوقائية للأجهزة الطبية بناءً على تعليمات الشركات المصنعة ومتابعة تنفيذها بفعالية.</li> <li >تطوير أساليب وإجراءات العمل الهندسية ومواكبة أحدث التطورات التقنية في مجال الأجهزة الطبية.</li> </ul> <h3 >إدارة الوثائق والتقارير</h3> <ul > <li >إعداد الوثائق والتقارير المتخصصة المتعلقة بالأعمال والمشروعات الهندسية ونسب تقدمها.</li> <li >عرض وتوضيح هذه التقارير وحفظها في قاعدة البيانات المخصصة وفقاً للسياسات والإجراءات المعتمدة في الشركة.</li> </ul> <h3 >المؤهلات والخبرات المطلوبة</h3> <ul > <li >درجة جامعية في هندسة الأجهزة الطبية أو مجال هندسي ذي صلة.</li> <li >خبرة عملية تتراوح بين <strong >0 إلى 1 سنة</strong> في مجال صيانة وتركيب الأجهزة الطبية.</li> <li >القدرة على تشخيص الأعطال الفنية وإعداد خطط الصيانة الوقائية.</li> <li >مهارات جيدة في إعداد التقارير الفنية والوثائق المتخصصة.</li> </ul> <h3 >تفاصيل إضافية</h3> <ul > <li ><strong>موقع العمل:</strong> حائل، المملكة العربية السعودية.</li> <li ><strong>نوع الوظيفة:</strong> دوام كامل.</li> <li ><strong>الراتب:</strong> غير معلن.</li> </ul></div>