وظائف هندسة طبية في قطر
٣١ وظائف شاغرة
قطر - الدوحة
Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana™ Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing Nav IQ™, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&D and manufacturing center in Doha, Qatar. To learn more about Akura Medical, please visit www.akuramed.com.<br>About Shifamed Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.<br>Description:<br>This position represents an exciting opportunity to join the Akura team at an early stage where you will creatively design and develop components, both consumable and capital equipment, of a blood clot removal system. The role focuses on mechanical design of various components and assemblies for catheter systems, a console, and cross-functional leadership from concept through high volume manufacturing. You will be responsible for the design, vendor relationships and testing per applicable standards. This is a full-time, on-site position at our Doha, Qatar office.<br>Responsibilities, Skills & Hands-On Experience:Lead design and development of plastic/composite and metallic parts from concept to high volume manufacturing; drive DFM/DFS, manufacturing and tooling decisions with suppliers. Drive the full mechanical lifecycle: requirements, concepts, prototyping, detailed design, V&V, and transition to production. Integrate mechanical designs with electronics, firmware, fluid, and user-interface elements in collaboration with cross-functional teams. Guide analysis (tolerance stacks, FEA, material selection, root-cause) on critical subsystems. Creative solutions and product designs to satisfy unmet clinical needs in thrombectomy. Be a primary contributor to the intellectual property position of the company via invention disclosures and prototypes to demonstrate reduction to practice. Interact with physicians to assist with product demonstrations and product testing. Effectively document work throughout the development process though design reviews, manufacturing instructions, test methods, and test reports. Expertise in design and development of medical devices. Expertise in electromechanical and mechanism design of durable medical devices. Substantial experience in design of higher volume disposable components. Substantial experience in design for molding and machining. Substantial experience in design for manufacturing. Pilot production experience. Expertise in product, tool and fixture design using Solid Works. Performance test apparatus and test method development. Process development on both a prototype and manufacturing level. Mentoring and assisting team members with less experience. Participating in lab and cleanroom environment builds. Process optimization and design of experiment based on statistical methodology. Selecting and managing suppliers, including understanding of capabilities, materials, and fabrication processes Working independently and in a project team setting. Supporting regulatory filings including writing technical sections and providing general technical input.<br>Education & Work Experience:Bachelor's Degree or higher in Mechanical/Biomedical Engineering. At least 15 years of experience in complex product development, including regulated products. Advanced Solid Works proficiency. Demonstrated track record as a lead/principal engineer or product design of medical devices from concept through launch. Strong expertise in injection molding and RIM molding (part design, materials, DFM, cosmetic and structural considerations). Strong experience with medical devices under FDA/ISO 13485 or equivalent regulatory frameworks. Previous experience working with clinical testing, trials, data collection, and statistical analysis.<br>Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.<br>NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.
قطر - الدوحة
Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana™ Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing Nav IQ™, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&D and manufacturing center in Doha, Qatar. To learn more about Akura Medical, please visit www.akuramed.com.<br><br>About Shifamed<br><br>Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.<br><br>Description:<br><br>This position represents an exciting opportunity to join the Akura team at an early stage where you will creatively design and develop components, both consumable and capital equipment, of a blood clot removal system. The role focuses on mechanical design of various components and assemblies for catheter systems, a console, and cross-functional leadership from concept through high volume manufacturing. You will be responsible for the design, vendor relationships and testing per applicable standards. This is a full-time, on-site position at our Doha, Qatar office.<br><br>Responsibilities, Skills & Hands-On Experience:<br><br>Lead design and development of plastic/composite and metallic parts from concept to high volume manufacturing; drive DFM/DFS, manufacturing and tooling decisions with suppliers. Drive the full mechanical lifecycle: requirements, concepts, prototyping, detailed design, V&V, and transition to production. Integrate mechanical designs with electronics, firmware, fluid, and user-interface elements in collaboration with cross-functional teams. Guide analysis (tolerance stacks, FEA, material selection, root-cause) on critical subsystems. Creative solutions and product designs to satisfy unmet clinical needs in thrombectomy. Be a primary contributor to the intellectual property position of the company via invention disclosures and prototypes to demonstrate reduction to practice. Interact with physicians to assist with product demonstrations and product testing. Effectively document work throughout the development process though design reviews, manufacturing instructions, test methods, and test reports. Expertise in design and development of medical devices. Expertise in electromechanical and mechanism design of durable medical devices. Substantial experience in design of higher volume disposable components. Substantial experience in design for molding and machining. Substantial experience in design for manufacturing. Pilot production experience. Expertise in product, tool and fixture design using Solid Works. Performance test apparatus and test method development. Process development on both a prototype and manufacturing level. Mentoring and assisting team members with less experience. Participating in lab and cleanroom environment builds. Process optimization and design of experiment based on statistical methodology. Selecting and managing suppliers, including understanding of capabilities, materials, and fabrication processes Working independently and in a project team setting. Supporting regulatory filings including writing technical sections and providing general technical input.<br><br><br>Education & Work Experience:<br><br>Bachelor's Degree or higher in Mechanical/Biomedical Engineering. At least 15 years of experience in complex product development, including regulated products. Advanced Solid Works proficiency. Demonstrated track record as a lead/principal engineer or product design of medical devices from concept through launch. Strong expertise in injection molding and RIM molding (part design, materials, DFM, cosmetic and structural considerations). Strong experience with medical devices under FDA/ISO 13485 or equivalent regulatory frameworks. Previous experience working with clinical testing, trials, data collection, and statistical analysis.<br><br><br>Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.<br><br>NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.
قطر - الدوحة
Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana™ Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing Nav IQ™, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&D and manufacturing center in Doha, Qatar. To learn more about Akura Medical, please visit www.akuramed.com.<br><br>About Shifamed<br><br>Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.<br><br>Description:<br><br>This position represents an exciting opportunity to join the Akura team at an early stage where you will creatively design and develop components, both consumable and capital equipment, of a blood clot removal system. The role focuses on mechanical design of various components and assemblies for catheter systems, a console, and cross-functional leadership from concept through high volume manufacturing. You will be responsible for the design, vendor relationships and testing per applicable standards. This is a full-time, on-site position at our Doha, Qatar office.<br><br>Responsibilities, Skills & Hands-On Experience:<br><br>Lead design and development of plastic/composite and metallic parts from concept to high volume manufacturing; drive DFM/DFS, manufacturing and tooling decisions with suppliers. Drive the full mechanical lifecycle: requirements, concepts, prototyping, detailed design, V&V, and transition to production. Integrate mechanical designs with electronics, firmware, fluid, and user-interface elements in collaboration with cross-functional teams. Guide analysis (tolerance stacks, FEA, material selection, root-cause) on critical subsystems. Creative solutions and product designs to satisfy unmet clinical needs in thrombectomy. Be a primary contributor to the intellectual property position of the company via invention disclosures and prototypes to demonstrate reduction to practice. Interact with physicians to assist with product demonstrations and product testing. Effectively document work throughout the development process though design reviews, manufacturing instructions, test methods, and test reports. Expertise in design and development of medical devices. Expertise in electromechanical and mechanism design of durable medical devices. Substantial experience in design of higher volume disposable components. Substantial experience in design for molding and machining. Substantial experience in design for manufacturing. Pilot production experience. Expertise in product, tool and fixture design using Solid Works. Performance test apparatus and test method development. Process development on both a prototype and manufacturing level. Mentoring and assisting team members with less experience. Participating in lab and cleanroom environment builds. Process optimization and design of experiment based on statistical methodology. Selecting and managing suppliers, including understanding of capabilities, materials, and fabrication processes Working independently and in a project team setting. Supporting regulatory filings including writing technical sections and providing general technical input.<br><br><br>Education & Work Experience:<br><br>Bachelor's Degree or higher in Mechanical/Biomedical Engineering. At least 15 years of experience in complex product development, including regulated products. Advanced Solid Works proficiency. Demonstrated track record as a lead/principal engineer or product design of medical devices from concept through launch. Strong expertise in injection molding and RIM molding (part design, materials, DFM, cosmetic and structural considerations). Strong experience with medical devices under FDA/ISO 13485 or equivalent regulatory frameworks. Previous experience working with clinical testing, trials, data collection, and statistical analysis.<br><br><br>Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.<br><br>NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.
قطر - الدوحة
Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana™ Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing Nav IQ™, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&D and manufacturing center in Doha, Qatar.<br>ABOUT SHIFAMEDFounded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.<br>Description:<br>This Manager / Sr. Manager, Regulatory Affairs will serve as a key member of the cross-functional team, partnering closely with Clinical, Quality, R&D, and Executive Leadership to support U. S. regulatory activities and lead global clinical studies and international market expansion. The ideal candidate brings strong FDA medical device experience combined with hands-on knowledge of international regulatory pathways, agency interactions, and clinical study support across Europe, the Middle East, and other global markets. This is a unique opportunity to help shape regulatory strategy for a clinical-stage medical device company as it expands global clinical activities, and prepares for international commercialization.<br>Responsibilities, Skills & Hands-On Experience:<br>Regulatory Strategy & Product Development:Develop and execute global regulatory strategies for Akura Medical's thrombectomy and catheter-based cardiovascular technologies. Serve as regulatory lead on cross-functional product development teams from concept through commercialization. Provide regulatory guidance on design controls, risk management, verification and validation activities, labeling, and product changes. Partner with Quality and R&D teams to ensure compliance with FDA, MDR, ISO 13485, and applicable international requirements. FDA Regulatory Affairs Lead preparation, review, and submission of U. S. regulatory filings, including IDE's, 510(k)'s, supplements, and other regulatory submissions as applicable. Monitor evolving FDA requirements and assess impact on development and commercialization plans. International Regulatory Expansion Develop regulatory strategies and market access plans for Europe, the Middle East, and other international markets. Support CE Mark and MDR-related activities in partnership with Notified Bodies and external regulatory consultants. Lead country-specific registration activities and regulatory submissions across key international markets including Qatar, UAE, Saudi Arabia, and other MENA countries. Establish and maintain relationships with regulatory authorities, notified bodies, and international regulatory partners. Clinical & Regulatory Operations Partner closely with Clinical Affairs to support global clinical studies, including IDE, PMCF, registries, and post-market studies. Provide regulatory guidance on protocol development, clinical study design, and regulatory approval pathways. Support regulatory submissions associated with clinical trial approvals across multiple countries and regions. Participate in investigator meetings, regulatory inspections, audits, and agency interactions. Agency Interactions & Compliance Represent the company during interactions with FDA, Notified Bodies, Ministries of Health, and other regulatory authorities. Support preparation for regulatory inspections and audits. Maintain awareness of evolving global regulatory requirements and communicate potential impacts to leadership. Contribute to regulatory intelligence activities and long-term market expansion planning. Cross-Functional Leadership Collaborate with Clinical, Quality, Manufacturing, Supply Chain, and R&D teams to ensure regulatory requirements are incorporated throughout the product lifecycle. Provide regulatory leadership for change assessments, design modifications, and lifecycle management activities. Support Executive Leadership with regulatory risk assessments, timelines, and strategic planning.<br>Qualifications & Experience:Bachelor's degree in Engineering, Life Sciences, Biomedical Engineering, or related field.10+ years of Regulatory Affairs experience within the medical device industry; cardiovascular, endovascular, or interventional products strongly preferred. Direct experience with FDA medical device submissions, including IDE's, PMA's, 510(k)'s, or PMA supplements. Experience supporting clinical-stage medical device programs and global clinical studies. Working knowledge of EU MDR, ISO 13485, ISO 14971, IEC 62304, and international regulatory frameworks. Experience interacting directly with regulatory agencies, notified bodies, and international health authorities. Familiarity with MENA regulatory pathways (Saudi SFDA, UAE MOHAP/DOH, Qatar MOPH, etc.) is highly desirable. Strong understanding of design controls, risk management, clinical evidence requirements, and regulatory strategy development. Excellent written, verbal, and presentation skills. Ability to thrive in a fast-paced, entrepreneurial environment and work effectively across global teams. Preferred Qualifications:Experience with thrombectomy, vascular intervention, pulmonary embolism, structural heart, or electrophysiology technologies. Prior experience supporting regulatory expansion into Europe, the Middle East, and emerging international markets. Experience participating in FDA meetings, regulatory inspections, and Notified Body audits.<br>Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.<br>NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.
قطر - الدوحة
Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana™ Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing Nav IQ™, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&D and manufacturing center in Doha, Qatar.<br>ABOUT SHIFAMEDFounded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.<br>Description:<br>This Manager / Sr. Manager, Regulatory Affairs will serve as a key member of the cross-functional team, partnering closely with Clinical, Quality, R&D, and Executive Leadership to support U. S. regulatory activities and lead global clinical studies and international market expansion. The ideal candidate brings strong FDA medical device experience combined with hands-on knowledge of international regulatory pathways, agency interactions, and clinical study support across Europe, the Middle East, and other global markets. This is a unique opportunity to help shape regulatory strategy for a clinical-stage medical device company as it expands global clinical activities, and prepares for international commercialization.<br>Responsibilities, Skills & Hands-On Experience:<br>Regulatory Strategy & Product Development:Develop and execute global regulatory strategies for Akura Medical's thrombectomy and catheter-based cardiovascular technologies. Serve as regulatory lead on cross-functional product development teams from concept through commercialization. Provide regulatory guidance on design controls, risk management, verification and validation activities, labeling, and product changes. Partner with Quality and R&D teams to ensure compliance with FDA, MDR, ISO 13485, and applicable international requirements. FDA Regulatory Affairs Lead preparation, review, and submission of U. S. regulatory filings, including IDE's, 510(k)'s, supplements, and other regulatory submissions as applicable. Monitor evolving FDA requirements and assess impact on development and commercialization plans. International Regulatory Expansion Develop regulatory strategies and market access plans for Europe, the Middle East, and other international markets. Support CE Mark and MDR-related activities in partnership with Notified Bodies and external regulatory consultants. Lead country-specific registration activities and regulatory submissions across key international markets including Qatar, UAE, Saudi Arabia, and other MENA countries. Establish and maintain relationships with regulatory authorities, notified bodies, and international regulatory partners. Clinical & Regulatory Operations Partner closely with Clinical Affairs to support global clinical studies, including IDE, PMCF, registries, and post-market studies. Provide regulatory guidance on protocol development, clinical study design, and regulatory approval pathways. Support regulatory submissions associated with clinical trial approvals across multiple countries and regions. Participate in investigator meetings, regulatory inspections, audits, and agency interactions. Agency Interactions & Compliance Represent the company during interactions with FDA, Notified Bodies, Ministries of Health, and other regulatory authorities. Support preparation for regulatory inspections and audits. Maintain awareness of evolving global regulatory requirements and communicate potential impacts to leadership. Contribute to regulatory intelligence activities and long-term market expansion planning. Cross-Functional Leadership Collaborate with Clinical, Quality, Manufacturing, Supply Chain, and R&D teams to ensure regulatory requirements are incorporated throughout the product lifecycle. Provide regulatory leadership for change assessments, design modifications, and lifecycle management activities. Support Executive Leadership with regulatory risk assessments, timelines, and strategic planning.<br>Qualifications & Experience:Bachelor's degree in Engineering, Life Sciences, Biomedical Engineering, or related field.10+ years of Regulatory Affairs experience within the medical device industry; cardiovascular, endovascular, or interventional products strongly preferred. Direct experience with FDA medical device submissions, including IDE's, PMA's, 510(k)'s, or PMA supplements. Experience supporting clinical-stage medical device programs and global clinical studies. Working knowledge of EU MDR, ISO 13485, ISO 14971, IEC 62304, and international regulatory frameworks. Experience interacting directly with regulatory agencies, notified bodies, and international health authorities. Familiarity with MENA regulatory pathways (Saudi SFDA, UAE MOHAP/DOH, Qatar MOPH, etc.) is highly desirable. Strong understanding of design controls, risk management, clinical evidence requirements, and regulatory strategy development. Excellent written, verbal, and presentation skills. Ability to thrive in a fast-paced, entrepreneurial environment and work effectively across global teams. Preferred Qualifications:Experience with thrombectomy, vascular intervention, pulmonary embolism, structural heart, or electrophysiology technologies. Prior experience supporting regulatory expansion into Europe, the Middle East, and emerging international markets. Experience participating in FDA meetings, regulatory inspections, and Notified Body audits.<br>Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.<br>NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.
قطر - الدوحة
Akura Medical, a Shifamed portfolio company, is advancing a differentiated platform for the treatment of venous thromboembolism (VTE), which affects up to 900,000 Americans each year. The company recently received US IDE approval for its QUADRA-PE study evaluating the Katana™ Thrombectomy System in acute pulmonary embolism patients. In parallel, Akura Medical is developing Nav IQ™, a software platform that transforms CT angiograms into 3D pulmonary vascular models to enhance visualization, procedural planning, and clot assessment towards better safety, efficacy, and ease of use. Akura has recently completed a $53 million first close of its Series C financing, led by the Qatar Investment Authority, supporting the launch of a joint venture and a new R&D and manufacturing center in Doha, Qatar.<br>ABOUT SHIFAMEDFounded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.<br>Description:<br>This Manager / Sr. Manager, Regulatory Affairs will serve as a key member of the cross-functional team, partnering closely with Clinical, Quality, R&D, and Executive Leadership to support U. S. regulatory activities and lead global clinical studies and international market expansion. The ideal candidate brings strong FDA medical device experience combined with hands-on knowledge of international regulatory pathways, agency interactions, and clinical study support across Europe, the Middle East, and other global markets. This is a unique opportunity to help shape regulatory strategy for a clinical-stage medical device company as it expands global clinical activities, and prepares for international commercialization.<br>Responsibilities, Skills & Hands-On Experience:<br>Regulatory Strategy & Product Development:Develop and execute global regulatory strategies for Akura Medical's thrombectomy and catheter-based cardiovascular technologies. Serve as regulatory lead on cross-functional product development teams from concept through commercialization. Provide regulatory guidance on design controls, risk management, verification and validation activities, labeling, and product changes. Partner with Quality and R&D teams to ensure compliance with FDA, MDR, ISO 13485, and applicable international requirements. FDA Regulatory Affairs Lead preparation, review, and submission of U. S. regulatory filings, including IDE's, 510(k)'s, supplements, and other regulatory submissions as applicable. Monitor evolving FDA requirements and assess impact on development and commercialization plans. International Regulatory Expansion Develop regulatory strategies and market access plans for Europe, the Middle East, and other international markets. Support CE Mark and MDR-related activities in partnership with Notified Bodies and external regulatory consultants. Lead country-specific registration activities and regulatory submissions across key international markets including Qatar, UAE, Saudi Arabia, and other MENA countries. Establish and maintain relationships with regulatory authorities, notified bodies, and international regulatory partners. Clinical & Regulatory Operations Partner closely with Clinical Affairs to support global clinical studies, including IDE, PMCF, registries, and post-market studies. Provide regulatory guidance on protocol development, clinical study design, and regulatory approval pathways. Support regulatory submissions associated with clinical trial approvals across multiple countries and regions. Participate in investigator meetings, regulatory inspections, audits, and agency interactions. Agency Interactions & Compliance Represent the company during interactions with FDA, Notified Bodies, Ministries of Health, and other regulatory authorities. Support preparation for regulatory inspections and audits. Maintain awareness of evolving global regulatory requirements and communicate potential impacts to leadership. Contribute to regulatory intelligence activities and long-term market expansion planning. Cross-Functional Leadership Collaborate with Clinical, Quality, Manufacturing, Supply Chain, and R&D teams to ensure regulatory requirements are incorporated throughout the product lifecycle. Provide regulatory leadership for change assessments, design modifications, and lifecycle management activities. Support Executive Leadership with regulatory risk assessments, timelines, and strategic planning.<br>Qualifications & Experience:Bachelor's degree in Engineering, Life Sciences, Biomedical Engineering, or related field.10+ years of Regulatory Affairs experience within the medical device industry; cardiovascular, endovascular, or interventional products strongly preferred. Direct experience with FDA medical device submissions, including IDE's, PMA's, 510(k)'s, or PMA supplements. Experience supporting clinical-stage medical device programs and global clinical studies. Working knowledge of EU MDR, ISO 13485, ISO 14971, IEC 62304, and international regulatory frameworks. Experience interacting directly with regulatory agencies, notified bodies, and international health authorities. Familiarity with MENA regulatory pathways (Saudi SFDA, UAE MOHAP/DOH, Qatar MOPH, etc.) is highly desirable. Strong understanding of design controls, risk management, clinical evidence requirements, and regulatory strategy development. Excellent written, verbal, and presentation skills. Ability to thrive in a fast-paced, entrepreneurial environment and work effectively across global teams. Preferred Qualifications:Experience with thrombectomy, vascular intervention, pulmonary embolism, structural heart, or electrophysiology technologies. Prior experience supporting regulatory expansion into Europe, the Middle East, and emerging international markets. Experience participating in FDA meetings, regulatory inspections, and Notified Body audits.<br>Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications.<br>NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.
Nasser Bin Khaled and Sons
قطر
<h2 class="h5">وصف الوظيفة</h2>
<div class="t-break" data-jb-field="description">
المسؤوليات الوظيفية<br><br> * تحديد وضمان قنوات توزيع جديدة، وشراكات استراتيجية، وتحالفات أعمال لتوسيع تغطية السوق.<br> * تطوير وتنفيذ استراتيجيات تطوير الأعمال بما يتماشى مع الأهداف التجارية للشركة، وخطط توسيع المحفظة، والمتطلبات الأساسية.<br> * تحليل اتجاهات السوق وأنشطة المنافسين واحتياجات العملاء والتقنيات الناشئة لتحديد فرص النمو وتعزيز موضع السوق.<br> * بناء والحفاظ على علاقات قوية مع الشركات الدولية والموردين لدعم تطوير المحفظة وتسجيل المنتجات والتخطيط التجاري والنمو التجاري.<br> * بناء وتطوير والحفاظ على علاقات قوية مع القادة الرؤى المؤثرين (KOLs)، والمهنيين الصحيين، ومالكي العيادات، وفرق الشراء، والموزعين، والشركاء الاستراتيجيين.<br> * دفع نمو المبيعات عبر محفظة الأدوية والتجميل من خلال تحقيق أهداف الإيرادات والربحية وحصة السوق.<br> * تحديد فرص تحسين تجربة العملاء، والعمليات التجارية، والكفاءة التجارية من خلال مبادرات التحسين المستمر.<br> * تحديد وتقييم والسعي وراء فرص تجارية جديدة ضمن قطاعات الأدوية والتجميل الطبي، بما في ذلك المستشفيات والعيادات ومراكز التجميل وممارسات الأمراض الجلدية وعيادات جراحة التجميل والصيدليات والمؤسسات الصحية.<br> * قيادة استراتيجيات إطلاق المنتجات وخطط التسويق بالتعاون مع فرق التسويق والشؤون الطبية والشؤون التنظيمية وسلسلة التوريد.<br> * إعداد وتقديم عروض أعمال مقنعة، وعروض منتجات، ومقترحات تجارية للمهنيين الصحيين وصانعي القرار.<br> * إعداد تقارير تطوير الأعمال الشهرية التي تغطي أداء المبيعات واكتساب العملاء وحالة خط الأنابيب ومعلومات السوق وتوقعات الإيرادات.<br> * أداء واجبات قسمية أخرى تتعلق بوظيفته حسب توجيه رئيس القسم.<br> * التعاون مع الأطراف الداخلية لضمان توفر المنتجات في الوقت المناسب والامتثال التنظيمي وتماشي الأسعار ونجاح onboarding للعملاء.<br> * تطوير والحفاظ على فهم شامل لمحفظة الأدوية والتجميل، بما في ذلك وضع المنتجات والأدلة السريرية وديناميكيات السوق والميزات التنافسية.<br> * جمع ونقل ملاحظات العملاء وذكاء المنافسين ورؤى السوق للإدارة العليا لدعم اتخاذ القرار الاستراتيجي وتوسيع المحفظة.<br> * الحفاظ على سجلات العملاء الدقيقة والمحدثة وأنشطة المبيعات وتتبع الفرص ضمن نظام إدارة علاقات العملاء (CRM).<br> * إدارة خط أنابيب المبيعات وفرص العملاء والتنبؤ وأنشطة تطوير الأعمال لضمان تحقيق KPIs باستمرار.<br> * تنظيم ودعم إطلاق المنتجات، والاجتماعات العلمية، وورش العمل، والمؤتمرات، والبرامج التعليمية لزيادة الوعي بالمنتج وتفاعل العملاء.<br> * المشاركة في تقديم العطاءات، والمفاوضات التجارية، ومناقشات التسعير، وإدارة العقود حيثما كان ذلك مناسباً.<br><br>المؤهلات<br><br>الهندسة biomedical أو مجال ذو صلة وثيقة.<br>المهارات<br><br> * القدرة على التكيف مع بيئة عمل سريعة الإيقاع وديناميكية.<br> * عقلية إبداعية والقدرة على التفكير خارج الصندوق.<br> * قدرات القيادة وإدارة الفريق المثبتة.<br> * مهارات تواصل وعرض ممتازة.<br> * الكفاءة في برامج المكتب القياسية (مثل حزمة Microsoft Office).<br> * مهارات إدارة المشاريع والتنظيم القوية.<br> * التفكير الاستراتيجي والقدرات التحليلية القوية.<br><br>الخبرة<br><br> * قطر، مجلس التعاون الخليجي<br> * خبرة سابقة في إدارة فرق المبيعات في قطاع الخدمات الطبية مع التركيز الأساسي على توليد الإيرادات والقيادات المحتملة الناجحة (معدات طبية، مشاريع المستشفيات ذات الصلة)<br> * خبرة لا تقل عن 7 سنوات ذات صلة<br><br>التعليم<br><br> * مؤهل جامعي ذي صلة أو أعلى حتى مستوى البكالوريوس<br>
</div><h2 class="h5">المهارات</h2>
<div data-jb-field="skills">* Identify and secure new distribution channels, strategic partnerships, and business alliances to expand market coverage.<br> * Develop and execute business development strategies aligned with the company's commercial objectives, portfolio expansion plans, and principal requirements.<br> * Analyze market trends, competitor activities, customer needs, and emerging technologies to identify growth opportunities and enhance market positioning.<br> * Build and maintain strong relationships with international principals and suppliers to support portfolio development, product registration, business planning, and commercial growth.<br> * Build, develop and maintain strong relationships with key opinion leaders (KOLs), healthcare professionals, clinic owners, procurement teams, distributors, and strategic partners.<br> * Drive sales growth across the pharmaceutical and aesthetic product portfolio by achieving revenue, profitability, and market share targets.<br> * Identify opportunities to improve customer experience, business processes, and commercial effectiveness through continuous improvement initiatives.<br> * Identify, evaluate, and pursue new business opportunities within the pharmaceutical and medical aesthetics sectors, including hospitals, clinics, aesthetic centers, dermatology practices, plastic surgery clinics, pharmacies, and healthcare institutions.<br> * Lead product launch strategies and commercialization plans in collaboration with Marketing, Medical Affairs, Regulatory Affairs, and Supply Chain teams.<br> * Prepare and deliver compelling business presentations, product demonstrations, and commercial proposals to healthcare professionals and decision-makers.<br> * Prepare monthly business development reports covering sales performance, customer acquisition, pipeline status, market intelligence, and revenue forecasts.<br> * Perform other department duties related to his/her position as directed by the Head of the Department.<br> * Collaborate with internal stakeholders to ensure timely product availability, regulatory compliance, pricing alignment, and successful customer onboarding.<br> * Develop and maintain a comprehensive understanding of the pharmaceutical and aesthetics portfolio, including product positioning, clinical evidence, market dynamics, and competitive advantages.<br> * Gather and communicate customer feedback, competitor intelligence, and market insights to senior management to support strategic decision-making and portfolio expansion.<br> * Maintain accurate and up-to-date customer records, sales activities, and opportunity tracking within the CRM system.<br> * Manage the sales pipeline, customer opportunities, forecasting, and business development activities to ensure consistent achievement of KPIs.<br> * Organize and support product launches, scientific meetings, workshops, conferences, and educational programs to increase product awareness and customer engagement.<br> * Participate in tender submissions, commercial negotiations, pricing discussions, and contract management where applicable.<br>
</div>
UrbaCon Contracting & Trading Company
قطر
<h2 class="h5">الوصف الوظيفي</h2>
<div class="t-break" data-jb-field="description">
<span><u><b>ملخص الوظيفة</b></u>
<br></span><p>لتشغيل معدات الأشعة بما في ذلك على سبيل المثال لا الحصر الأشعة السينية، التصوير بالمقطعية، Dexa، التصوير الشعاعي للثدي، الفلوروسكوبي، الرنين المغناطيسي، والتدخلات وفق ما يلزم من معدات CT لأغراض تشخيصية. لإعداد ومساعدة المرضى أثناء فحوصات واختبارات الأشعة. لإعداد والحفاظ على سجلات الأشعة.</p><br>
<br><br><u><b>المسؤوليات الوظيفية 1</b></u>
<br><p>يجمع معلومات رئيسية من المريض والعائلة ومقدم الرعاية والممرضين خاصة بالامتحان الجاري للمساعدة في التشخيص الصحيح من قبل المزود.</p><br>
<p>يوجه المريض أو العائلة أو مقدم الرعاية بشأن مدى وتفصيل كل إجراء، بما في ذلك الموافقة المستنيرة بالإضافة إلى تعليمات ما قبل وما بعد الإجراءات.</p><br>
<p>يضمن أن الإجراء الصحيح يُدار للمريض.</p><br>
<p>يستشير المزود عند الحاجة.</p><br>
<p>يحافظ على مستويات الجرد الدقيقة لجميع المستلزمات كما هو مطلوب.</p><br>
<p>يجري فحص المعدات يومياً.</p><br>
<p>يشارك في تناوب الاتصالات حسب الحاجة.</p><br>
<p>يمارس الإرشادات الخاصة بسياسة ALARA (أقصى ما يمكن تحقيقه بأمان).</p><br>
<p>يساعد في يوميات المرضى في خدمات الأشعة العامة بالتعاون مع فني الأشعة II والمشرف لضمان سير القسم بكفاءة.</p><br>
<p>يساعد في تطبيق جميع السياسات والإجراءات المتعلقة بالأشعة العامة.</p><br>
<p>يواكب التطورات في الأشعة العامة.</p><br>
<p>يجري فحوصات عالية الجودة كما يطلبه الأطباء المعنيون وفق سياسات وإجراءات القسم.</p><br>
<p>يضمن أن جميع المرضى الذين يتم فحصهم يحصلون على مستوى رعاية عالي.</p><br>
<p>يتدرب ويعمل في مجالات أخرى من القسم تعتبر مناسبة.</p><br>
<p>يؤدي واجبات ومسؤوليات أخرى كما يتم تكليفه.</p><br>
<p>يبلغ المرضى بدقة مكان وزمان توفر نتائجهم ومن سيقدمها لهم.</p><br> <br><u><b>المسؤوليات الوظيفية 2</b></u>
<br><p>يعمل بدقة للحفاظ على مستوى عالٍ من التصوير وتقليل وقت انتظار المريض بما يوازي مع معايير الجودة.</p><br>
<p>يضمن أن معايير الرصد توفر خدمة عالية الجودة للعناية بالمريض والأداء الفني والتقارير.</p><br>
<p>يشارك في برنامج ضمان الجودة للمعدات وحماية الأشعة، مع الحفاظ على سجلات دقيقة والإبلاغ عن المشاكل إلى المدير.</p><br>
<p>يوثق جميع عيوب المعدات للـ RSO والمدير والقسم الطبي الحيوي حسب سياسة الشركة.</p><br>
<p>ينشئ ويحافظ على علاقات عمل جيدة مع جميع أعضاء قسم التصوير الطبي ويعمل بشكل إيجابي لتطوير فريق متماسك.</p><br>
<p>يتواصل مع اختصاصيي الأشعة.</p><br>
<p>يعزز علاقات جيدة مع الأطباء المحيلين، وأقسام المستشفى الأخرى والمنظمات الخارجية لضمان الحفاظ على سمعة قسم التصوير الطبي ومجموعة Elegancia للرعاية الصحية.</p><br>
<p>أن يكون على دراية كاملة بنظام إدارة الأشعة، والطريقة المحوسبة لتوثيق المرضى والفحوصات.</p><br>
<p>يضمن الحفاظ على أنظمة الحجز والمعلومات والتقارير والأرشفة وتطويرها بشكل فعال.</p><br>
<p>يتعهد بالقيام بأي مهام يعينها المدير/المشرف في قسم التصوير الطبي.</p><br>
<p>يضمن أن خصوصية المرضى لا تُخل.</p><br> <br><br><b>المسؤوليات الإضافية 3</b>
<br><br><u><b>معرفة العمل & المهارات</b></u>
<br><p>مهارات تواصل مميزة ومهارات خدمة المرضى والتعامل بين الأشخاص.</p><br>
<p>القدرة على تشغيل وفهم تكنولوجيا ومعدات التصوير الشعاعي.</p><br>
<p>القدرة البدنية على الوقوف لفترات طويلة وتشغيل الآلات الثقيلة بدون مساعدة.</p><br>
<p>المرونة للعمل في المناوبات وعطلات نهاية الأسبوع والليل والعطل.</p><br>
<br><br><u><b>خبرة العمل</b></u>
<br><p>خبرة لا تقل عن سنتين في الأشعة (مطلوبة).</p><br>
<p>خبرة لا تقل عن سنة في GCC (مفضل).</p><br>
<br><br><u><b>الكفاءات</b></u>
<br>سرعة التكيف<br>طلاقة AI<br>لوائح الامتثال والرعاية الصحية L2<br>التواصل مع المرضى وخدمة العملاء L2<br>التشريح والفسيولوجيا L2<br>وضع المريض وحماية الأشعة L2<br>سلامة الإشعاع وحمايته L2<br>القيادة<br>الجودة<br>المرونة<br><br><br><u><b>التعليم</b></u>
<br>شهادة بكالوريوس في أي مجال ذي صلة<br><br><br><br>
</div>
قطر - الدوحة
Job Description<br><br>At a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate, the success of large, complex global health companies requires regulatory leaders who are deeply steeped in the public and private levers that impact this industry. To remain competitive in this rapidly changing landscape, organizations require regulatory affairs professionals who can navigate complex and fast-changing laws, regulations, and public policies across the globe.<br><br>In this context, we are looking for regulatory affairs experts in the med-tech space to play a key role in driving Oracle's success and competitiveness in the healthcare and life sciences sector.<br><br>You will work primarily with the Oracle Health & Life Sciences business units but will also interact with all Oracle business units selling products to the health and life sciences industries. This role requires an individual who can keep up with the fast-paced environment of software development and an evolving regulatory landscape. For this role we are seeking a regulatory strategist who is collaborative, a creative problem solver, and dedicated to excellence in their work.<br><br>What You’ll Do:<br><br> Work closely with Oracle’s product engineering teams to assess product functionality and develop regulatory strategy for Middle East and Africa countries. Collaborate cross-functionally to create and manage submissions for health authorities including SFDA (Saudi Arabia), MOHAP (United Arab Emirates), MOPH (Qatar), NHRA (Bahrain), SAHPRA (South Africa), NAFDAC (Nigeria), EDA (Egypt) and PPB (Kenya) ensuring on going compliance with regulatory authorities. Maintain regulatory documentation, technical files, and post market surveillance activities ensuring ongoing compliance with applicable regulations. Support internal and external audits to identify, evaluate, disclose, and appropriately remedy risks and deficiencies. Serve as a subject matter expert for internal clients with interpretation of applicable standards, regulations, and use of the quality management system. Manage regulatory and compliance related projects for Health-related products. Review and recommend changes to labeling, marketing materials, clinical protocols, design processes, and procedures to maintain regulatory and quality compliance. Maintain compliance with changing regulatory requirements across global markets that impact to our businesses, regulatory affairs function, and quality/compliance programs. Build effective working relationships with regulatory agencies, affiliates, and cross-functional stakeholders to support aligned and practical regulatory outcomes. <br><br><br>Preferred Qualifications:<br><br> Bachelor’s degree in pharmacy, Biology, Biomedical Engineering, Engineering, Life Sciences, Health Sciences, or a related field. Experience with SaMD in areas such as Regulatory Affairs, Quality Compliance, Product Development, etc. in medical device industry or equivalent. Experience authoring submissions across assigned Middle East and Africa market required. Experience with sustaining and new product development is ideal. Comprehensive knowledge of regulatory requirements and processes across Middle East and Africa countries, with demonstrated experience interpreting local regulations and supporting market access, lifecycle compliance, and health authority engagements. Strong problem-solving, planning, and organizational skills, with the ability to manage multiple priorities and work independently in a fast-paced, cross-cultural environment. Experience in working within a quality management system, preferably with ISO 13485, ISO 14971, 60601, 62304, 21 CFR parts 1000/1001, Understands continual improvement and risk management. Excellent written and verbal communication skills. Experience engaging with regional trade associations, industry groups, or regulatory forums. Ability to adjust and adapt to changing priorities in a dynamic environment. Ability to perform in a fast-paced and continually evolving business environment. <br><br><br>Responsibilities<br><br>Performs evaluation of internal operations, controls, communications, risk assessments and maintenance of documentation as related to regulatory compliance and recommends appropriate changes. Conducts and facilitates internal and external audits to identify, evaluate, disclose and appropriately remedy risks and deficiencies. Coordinates the preparation of and may prepare document packages for regulatory submissions from all areas of company as well as for internal and external audits and inspections. May serve as point of contact for interactions with regulatory agencies for defined matters. Support the creation of a comprehensive risk management and/or quality management, and regulatory oversight program, including specifications for product and service design aligned with Oracle Software Security Assurance and Security Architecture, and/or Quality Management systems. Review specifications. Develop training for GBU development, cloud services, services and operations teams on industry regulatory specifications applicable to their products and services. Execute risk assessments and evaluate risks to the business and develop risk mitigation strategies. Identify industry requirements applicable to Oracle GBUs, and work with members of GBU development, cloud services, services and operations teams to incorporate applicable industry regulatory standards, Oracle security and/or quality policies and customer-contractual obligations into GBU processes and standards. Coordinate industry and regulatory certifications, including managing certification vendors (e.g., PCI, HIPAA,HITECH, ISO, SOC2). Build security documentation and collateral for customers and internal users allowing security to be a differentiator in this GBUs. Build management level metrics and reporting for activities that are owned by the Risk Manager. Execute a vendor security and/or quality management program.<br><br>Qualifications<br><br>Career Level - IC4<br><br>About Us<br><br>Only Oracle brings together the data, infrastructure, applications, and expertise to power everything from industry innovations to life-saving care. And with AI embedded across our products and services, we help customers turn that promise into a better future for all. Discover your potential at a company leading the way in AI and cloud solutions that impact billions of lives.<br><br>True innovation starts when everyone is empowered to contribute. That’s why we’re committed to growing a workforce that promotes opportunities for all with competitive benefits that support our people with flexible medical, life insurance, and retirement options. We also encourage employees to give back to their communities through our volunteer programs.<br><br>We’re committed to including people with disabilities at all stages of the employment process. If you require accessibility assistance or accommodation for a disability at any point, let us know by emailing accommodation-request_mb@oracle.com or by calling 1-888-404-2494 in the United States.<br><br>Oracle is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans’ status, or any other characteristic protected by law. Oracle will consider for employment qualified applicants with arrest and conviction records pursuant to applicable law.
قطر - الدوحة
Scale تُمكّن موجة الذكاء الاصطناعي التوليدي من خلال توفير البيانات والبنية التحتية للشركات لبناء نماذج أساسية واسعة النطاق. يتغير عالم AI بسرعة، وتقوم Scale بالنمو لتلبية هذه الطلبات السريعة عبر الأسواق العالمية، بما في ذلك توسيع الأعمال في القطاع العام عبر منطقة أوروبا والشرق الأوسط وأفريقيا. تسعى Scale إلى تعيين قائد Assurance في أوروبا والشرق الأوسط وأفريقيا لدفع برامج الضمان عبر قطاع Scale العام وقطاعه التجاري في هذه المنطقة. وبالتبعية لرئيس Assurance العالمي، هذا دور مساهم فاعل بيده عمله وبسلطة كبيرة. ستقوم بتصميم وامتلاك ضوابط خاصة بمنطقة أوروبا والشرق الأوسط وأفريقيا ضمن إطار عمل الضمان العالمي لـ Scale، مع البقاء متماشياً بشكل وثيق مع مكتبة الضوابط العالمية وجداول التقارير. ستكون جزءاً من فريق GRC العالمي وتعمل عبر القطاع العام العالمي والمؤسسات والأمن والهندسة والمنتج والشؤون القانونية لتوفير تراخيص وتصديقات ونتائج ضمان للزبائن خاصة بالإقليم في أوروبا والشرق الأوسط وأفريقيا، مع تركيز على أسواق دول مجلس التعاون الخليجي والمملكة المتحدة والاتحاد الأوروبي. ستقوم بـ<br><br>المهمة الرئيسية<br><br>قيادة برامج الضمان الإقليمية عبر الخليج والمملكة المتحدة، بما في ذلك NCSA قطر للمعلومات الأساسية (NIA)، NCA السعودية لضوابط الأمن السيبراني الأساسية (ECC)، DESC الإمارات للتنظيم الأمني للمعلومات (ISR)، وUK Cyber Essentials Plus وDefence Cyber Certification (DCC) وNCSC Secure by Design (SdB). ستتولى رسم خرائط الضوابط وجمع الأدلة وتحليل الثغرات وما إلى ذلك، مع إدارة جداول التصديق والتقديم للمراجعين المعتمدين عند الحاجة. العمل مع فريق GRC العالمي للحفاظ وتجديد الشهادات الحالية لـ Scale والحصول على شهادات جديدة، بما في ذلك SOC 2 وISO 27001 وISO 42001 وISO 9001. كما ستتولى توسيع نطاقها إلى العمليات الدولية وعلى مستوى أوروبا والشرق الأوسط وأفريقيا، بما في ذلك للمناقصات الدفاعية المرتبطة بـ NATO. تصميم والحفاظ على ضوابط خاصة بـ EMEA، وتكييف إطار الضوابط العالمي لـ Scale مع المتطلبات التنظيمية والزبونية السارية، بما في ذلك الإقامة البيانية ومتطلبات القطاع (مثلاً قطاع الصحة)، وتحديد أماكن تطابق الضوابط الحالية مع المعايير المحلية وأين تكون هناك حاجة لضوابط جديدة أو أدلة إثبات. تحديد الأولويات وتوقيتات تشغيل لسير عمل ضمان EMEA، بما في ذلك الاستلام وجمع الأدلة والمتابعة مع مالكي الضوابط وتتبع الإصلاحات وإدارة المواعيد النهائية، مع تقارير التقدم عبر لوحات القيادة العالمية للضمان لدى Scale. دعم أنشطة ضمان عملاء القطاع العام في EMEA، بما في ذلك الاستبيانات الأمنية وردود إجراءات التوافق ومسارات نقاش ضمان أمام العملاء وإدخال التوافق في عروض العطاءات وعمليات الالتقاط حيث تمثل الجاهزية للضمان حاجزاً للمشتريات. التعاون مع الشؤون القانونية بشأن التزامات الضمان القائمة على العقود في EMEA والعلاقات المتقاطعة مع حماية البيانات وحوكمة AI (مثل GDPR وQatar PDPPL وEU AI Act) والارتفاعات الحساسة التي تشمل الجهات التنظيمية السيادية. إدارة العلاقات مع مدققين ومقييمين وجهات اعتماد خارجية ومقابلات تنظيمية في EMEA. دعم عمليات التدقيق الداخلية والخارجية عبر EMEA والتقرير إلى رئيس Assurance العالمي عن صحة البرنامج والمخاطر الرئيسية وجداول زمن التصديق والتطورات التنظيمية الإقليمية. <br><br>من الأفضل أن تمتلك<br><br>7+ سنوات خبرة في امتثال الأمن السيبراني أو GRC أو ضمان القطاع العام أو تدقيق تكنولوجيا المعلومات أو أمن السحابة أو أدوار ذات صلة، مع تعرض مهم لأسواق EMEA. خبرة في تنفيذ برامج ضمان حكومية أو قطاع عام في المملكة المتحدة أو الاتحاد الأوروبي أو مجلس التعاون الخليجي، بما في ذلك العمل مع هيئات التصديق الخارجية أو مقيمين حكوميين أو مسؤولين مخولين. دراية عميقة بأحد أو أكثر من: UK Cyber Essentials/Cyber Essentials+، ISO 27001، ISO 9001، ISO 42001، SOC 2، أو أطر مكافئة، ومع أنظمة الأمن السيادي في الخليج (مثلاً قطر NCSA NIA، المملكة العربية السعودية SCCC/NCA، الإمارات DESC/NESA). إلمام بمطالب حماية البيانات وحوكمة الذكاء الاصطناعي السارية في EMEA وكيف تترجم إلى ضوابط تقنية وتنظيمية. خبرة في إدارة خرائط الضوابط وجمع الأدلة وتتبع الإصلاح وتنسيق التدقيق عبر فرق الهندسة والبنية التحتية الموزعة. خبرة في بيئات السحابة (AWS/Firebase/Azure/GCP) والقدرة على تقييم بنية السحابة مقابل متطلبات الامتثال. مهارات تواصل قوية وحكم سليم في التصعيد والقدرة على العمل باستقلالية في منطقة مع الحفاظ على التوافق مع برنامج عالمي. <br><br>مفضل وجوده<br><br>شهادات ذات صلة مثل CISSP وCISM وCISA وISO 27001 Lead Auditor وISO 42001 Internal Auditor أو CCSP. خبرة في معايير ضمان المعلومات لحلف الناتو أو متطلبات الشراء الدفاعي. إلمام بمتطلبات تنظيمية خاصة بقطاع الصحة في EMEA أو الأجهزة الطبية، خاصة في الخليج والمملكة المتحدة. معرفة عملية بالعربية. تصريح UK SC أو DV، أو الأهلية للحصول على تصاريح أمن حكومية معادلة في EMEA. خبرة في شركة Big 4 أو شركة تقنية ذات نمو عالي. <br><br>بالنسبة للراغبين في التقديم من قطر: الإقامة والعمل في قطر يتطلبان تصاريح (فيزا وتصاريح) معينة تصدرها السلطات القطرية. كجزء من عملية التقديم، سيُطلب من المرشحين تقديم معلومات شخصية، بما في ذلك وضع الإقامة والجنسية، وهو مطلوب لمعالجة الفيزا. يتم جمع هذه المعلومات فقط لأغراض الامتثال للهجرة ولن تُستخدم كمعيار في أي قرار توظيف ما لم يكن ذلك مسموحاً قانونياً. إصدار الفيزا بتقدير من السلطات القطرية. إذا نجحت في التقديم، سيتعين عليك تقديم الوثائق المطلوبة من Scale والسلطات للحصول على التصاريح اللازمة للعيش والعمل في قطر، وستتعاون Scale مع المرشحين الناجحين لدعم عملية طلب الفيزا. <br><br>يرجى ملاحظة: سياساتنا تشترط فتره انتظار 90 يوماً قبل إعادة النظر في المرشحين لنفس الدور. وذلك لضمان تقييم عادل وشامل لجميع المتقدمين. <br>عنّا:<br><br>في Scale، رسالتنا هي تطوير أنظمة AI موثوقة للقرارات الأكثر أهمية في العالم. منتجاتنا توفر البيانات عالية الجودة وتقنيات كاملة النطاق التي تدفع نماذج القياس الرائدة في العالم، وتساعد الشركات والحكومات على بناء وتوزيع ومراقبة تطبيقات AI التي تحقق أثرًا حقيقيًا. نعمل بشكل وثيق مع قادة الصناعة مثل Meta وErnst & Young وMayo Clinic وTime Inc. وحكومة قطر والجهات الأمريكية بما في ذلك الجيش والقوات الجوية. نحن نقوم بتوسيع فريقنا لتسريع تطوير تطبيقات AI. <br><br>نؤمن بأن على الجميع أن يتمكنوا من جلب أنفسهم كاملة للعمل، وهذا سبب فخرنا كمكان عمل شامل ومتكافئ الفرص. نحن ملتزمون بمبدأ المساواة في فرص العمل بغض النظر عن العرق أو اللون أو الأصل أو الدين أو الجنس أو الأصل القومي أو التوجه الجنسي أو العمر أو الجنسية أو الحالة الاجتماعية أو الإعاقة أو الهوية الجنسية أو حالة المحارب القديم. <br><br>نلتزم بتوفير التسهيلات المعقولة للمتقدمين ذوي الإعاقات الجسدية والذهنية. إذا كنت بحاجة إلى مساعدة و/أو تسهيل معقول في عملية التقديم أو التوظيف بسبب الإعاقة، يرجى التواصل معنا على accommodations@scale.com. الرجاء الاطلاع على ملصق Know Your Rights الخاص بوزارة العمل الأمريكية لمعلومات إضافية.<br><br>نلتزم بمزودي شفافية الأجور للوزارة الأمريكية للعمل. <br><br>يرجى ملاحظة: نجمع ونحتفظ ونستخدم البيانات الشخصية لأغراض أعمالنا المهنية، بما في ذلك إعلامك بفرص عمل قد تهمك ومشاركتها مع شركائنا. نحد من البيانات الشخصية التي نجمعها إلى ما نراه مناسباً وضرورياً لإدارة احتياجات المتقدمين، وتقديم خدماتنا، والامتثال للقوانين المعمول بها. أي معلومات نجمعها فيما يتعلق بطلبك ستعامل وفق سياساتنا وبرامجنا الداخلية المصممة لحماية البيانات الشخصية. رجاءً اطلع على سياسة الخصوصية لمعلومات إضافية.
Weill Cornell Medicine-Qatar
قطر
<h2 class=\"h5\">وصف الوظيفة</h2>
<div class=\"t-break\" data-jb-field=\"description\">
<p>ملخص المنصب</p><p>يتولى المنصب تصميم وتنفيذ وتفسير البحوث المعملية المتعلقة بالأيض السرطاني والآليات الجزيئية لتقدم الورم، مع دمج علم الجينوم الوظيفي، وتحليلات الأيض، والبيولوجيا التجريبية.</p><p>مسؤوليات الوظيفة</p><ul><li>يصمّم ويجري تجارب مخبرية مستقلة للتحقيق في أيض السرطان وتقدم المرض.</li><li>يشارك مع الباحثين الرئيسيين وفرق البحث متعددة التخصصات في تطوير تصاميم الدراسات وتعريف الأساليب التجريبية المتوافقة مع أهداف البحث.</li><li>يؤدي ويُحسّن التقنيات الجزيئية والخلوية، بما في ذلك تحرير الجين CRISPR-Cas9 واختبارات الخلايا.</li><li>يقوم بإجراء اختبارات حيوية وكيميائية وظيفية، بما في ذلك تحليل نشاط الإنزيم ومسارات الأيض.</li><li>يقوم بدراسات حية في نماذج الفئران، مع التأكد من الامتثال للمعايير المؤسسية والأخلاقية والتنظيمية.</li><li>يحلل ويفسر البيانات التجريبية ويساهم في نتائج الدراسة.</li><li>يُعد التقارير والرسوم البيانية والوثائق العلمية؛ يكتب وينشر النتائج في مجلات محكمة المراجعة.</li><li>يقدم نتائج البحث في الاجتماعات الداخلية والمؤتمرات العلمية الخارجية.</li><li>يوجه ويدعم الآخرين ضمن الفريق ومجتمع الطلاب حسب الحاجة.</li><li>يحافظ على سجلات وملاحظات مخبرية دقيقة ومنظمة.</li><li>يراجع الأدبيات العلمية ليُ Inform التصميم التجريبي وتحديد مجالات للتحسين.</li><li>يؤدي واجبات أخرى ذات صلة كما تُكلفه.</li></ul><p><br></p> </div><h2 class=\"h5\">المهارات</h2>
<div data-jb-field=\"skills\"><p>التعليم والخبرة</p><p>دكتوراه في علم سرطان، الكيمياء الحيوية، علم الأحياء الجزيئي، أو مجال ذي صلة، مع خبرة ذات صلة بعد التأهيل.</p><p>المعرفة والمهارات والقدرات</p><ul><li>خلفية قوية في أبحاث السرطان ويفضّل أبحاث أيض السرطان أو المسارات الكيميائية الحيوية.</li><li>معرفة واسعة بالتقنيات الجزيئية والخلوية، بما في ذلك تحرير الجين CRISPR-Cas9، زراعة الخلايا، الاختبارات الوظيفية والكيميائية الحيوية، تحليل نشاط الإنزيم، والدراسات خارج الجسم (مثل نماذج الفئران).</li><li>معرفة عملية بالنهج الأيضية المتعددة-الأوميكس، مع فهم لميتابوليز الميتوكوندري، علم الأحمر الأكسدي، أو المسارات ذات الصلة هو ميزة.</li><li>قدرة قوية على ربط النتائج التجريبية بالآليات البيولوجية الأساسية.</li><li>مهارات اتصال وتفاعل عالية، مع القدرة على التعاون مع فرق متعددة التخصصات.</li><li>إتقان حزمة Microsoft Office (Word، Excel، PowerPoint، Outlook؛ R أو أدوات مماثلة ميزة).</li></ul><p><br></p></div>