Oncology Medical Advisor

Join AbbVie, a global biopharmaceutical leader, as an Oncology Medical Advisor. In this pivotal role, you will collaborate with multidisciplinary teams to drive innovative oncology solutions. Your expertise will guide clinical strategies, ensuring we deliver the highest quality of care to patients.

We are seeking a dedicated Medical Manager specializing in Oncology to join our team at AbbVie. In this pivotal role, you will be responsible for overseeing clinical development and ensuring the successful implementation of our oncology programs. You will work closely with cross-functional teams to drive the scientific strategy and support our commitment to advancing patient care in oncology.

Join our dynamic team as a Medical Advisor at AbbVie in Budapest, where you will play a crucial role in providing medical expertise and support. In this position, you will be responsible for engaging with healthcare professionals, developing strategic medical plans, and ensuring the delivery of high-quality healthcare solutions to our patients.

Join AbbVie, a global biopharmaceutical leader, as a Medical Advisor in Budapest, where you'll play a pivotal role in supporting our mission to improve patients' lives. As part of our dynamic team, you will engage in scientific discussions, support clinical development, and collaborate with healthcare professionals to ensure the safe and effective use of our innovative therapies.

AbbVie Inc. is hiring a Medical Science Liaison to join its team in Budapest. This position acts as a key scientific contact for healthcare professionals, sharing current information about AbbVie’s therapies. Role overview The Medical Science Liaison provides scientific expertise to support patient care. The role involves communicating clinical data and insights, helping healthcare professionals stay informed about AbbVie’s treatment options. Impact This work contributes to improved health outcomes and aligns with AbbVie’s mission to advance patient care through science and collaboration.

Role overview Santen is hiring a Medical Representative in Budapest. This role centers on promoting Santen’s pharmaceutical products and supporting healthcare professionals with up-to-date information and resources. What you will do Build and maintain relationships with healthcare professionals in the region Share detailed, accurate information about Santen’s product portfolio Ensure healthcare providers have the resources needed to support patient care

About the Role Bosch Group is seeking an Administrative Intern for its Medical Center in Budapest. This internship offers practical experience in a healthcare administrative setting. The intern will help with daily administrative tasks and support the medical staff to keep the center running smoothly. What You Will Do Assist with a range of administrative duties Support healthcare professionals in their daily work Help maintain efficient operations throughout the center Location Budapest, onsite at the Bosch Group Medical Center

Join our esteemed partner, a leading global healthcare manufacturer, dedicated to the development of life-saving and life-enhancing medical devices within a highly regulated environment. With a robust engineering culture and a commitment to long-term product development, this company provides a stable work environment where your software solutions can make a direct impact on real-world patient outcomes.Key Responsibilities:Design and develop software for medical devices, emphasizing embedded systems and desktop applications.Craft and implement user interfaces utilizing XAML-based technologies such as WPF or Avalonia.Collaborate with international engineering teams throughout the entire product lifecycle.Engage in architectural discussions and suggest enhancements to existing systems.Adopt and promote modern development practices, including Clean Code, Test-Driven Development (TDD), and code reviews.Create and maintain technical documentation adhering to regulatory standards.Acquire domain knowledge in medical devices and associated development processes.

Our client is at the forefront of product innovation, focusing on the development and optimization of advanced products and production lines through close collaboration with customers and partners. They also provide expert consulting services for production support, optimization, validation, project management, and quality assurance, serving leading international companies within their sectors.Position Overview:As a Validation Engineer, you will be instrumental in verifying that products, systems, and processes adhere to requisite standards and regulations prior to market launch or implementation. You will ensure that all products, equipment, systems, and processes align with industry regulations, including FDA and ISO standards. This position entails crafting and executing validation plans, performing tests, and documenting outcomes to validate compliance and operational effectiveness.Key Responsibilities:Develop User Requirement Specifications (URS), Design Qualifications (DQ), Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.Create validation protocols for systems, equipment, and processes.Conduct qualification tests and execute risk assessments and gap analyses on systems and processes, including pFMECA and hazard analyses.Ensure that documentation adheres to industry standards such as FDA, ISO, and GMP.Identify validation deviations and collaborate with Quality Assurance teams to propose corrective actions.You will ensure that all validation efforts meet applicable regulatory requirements (e.g., FDA 21 CFR Part 11, ISO 9001, ISO 13485) and work in partnership with Quality Assurance and Regulatory Affairs to maintain compliance. Additionally, you will collaborate closely with R&D and manufacturing to integrate validation processes into project workflows and continuously analyze validation processes for improvement opportunities.

Who Are We?The Laba Group is one of the largest EdTech companies in Europe, dedicated to education. Currently, we have over 700 employees working across 8 markets with a shared mission to provide up-to-date, real knowledge to those eager to grow.Over the past decade, we have launched more than 1400 courses, educating over 200,000 students worldwide. Additionally, we have developed three distinct online educational brands:Laba – Business courses supporting professional development.Skvot – An online school for creative professions.robot_dreams – A platform for initiating and advancing IT careers.Our goal is to become a unicorn company, and our sales team plays a crucial role in achieving this .We are currently seeking talented sales professionals to join our team and work with either the Laba or robot_dreams educational brands.If you want to build a career in sales and are persistent, we are ready to invest in you even if you lack experience. We will teach you sales techniques and provide ongoing support from a sales trainer to help you catch up and surpass the entire team.

Join our esteemed partner, a leader in international accounting services and business consulting, as a VAT Consultant specializing in VAT matters. Your role will encompass the following responsibilities:Preparation and review of advisory letters addressing VAT-specific inquiries;Preparation and auditing of VAT returns, community summary reports, Intrastat reports, and domestic summary declarations;Participation in tax audit processes for corporations;Assisting clients during tax audits, including coordination with tax authorities and the preparation of appeal materials;Offering VAT-focused support for tax-related technological solutions;Mentoring and providing professional oversight to junior colleagues involved in VAT projects.

Your ResponsibilitiesParticipate in the development processes of life-saving and quality-of-life enhancing medical devices, including dialysis machines.Design and continuously refine the testing strategy for the product line.Define testing processes, tools, and methodologies while adhering to relevant standards.Plan and coordinate the work of the testing team.Track and analyze verification and validation reports, errors, and feedback.Coordinate projects involving multiple locations.

About the Role mpsolutions is seeking an Embedded C++ Developer to join its medical technology division in Budapest. The team focuses on developing solutions that support life-sustaining therapies, especially for chronic dialysis. Work involves creating safe, reliable medical devices that meet strict regulatory and quality standards. Collaboration spans multiple engineering disciplines and international partners to drive ongoing innovation in patient care technology. Main Responsibilities Design and develop products or components for the chronic dialysis technology portfolio. Analyze and maintain both functional and system concepts, including system and component requirements. Coordinate with internal teams and external partners on product architecture, technology choices, application, and system functionality. Prepare and present system design options based on defined requirements and architecture. Model system designs using Enterprise Architect, then integrate generated code into control applications. Verify system designs through prototype testing. Support engineering teams and the verification and validation (V&V) group during implementation, verification, and validation of requirements. Location Budapest, Budapest, Hungary

Join our innovative team as a QA Automation EngineerSentec AG, a pioneering Swiss-American medical device company, specializes in advanced respiratory care solutions. Established in 1999, we leverage cutting-edge technology and scientific research to enhance the lives of respiratory patients across various care environments.Our mission is to drive transformative changes in clinical practices that address the challenges faced by respiratory patients, improve health outcomes, and reduce healthcare costs. We develop and manufacture all our products in-house, focusing on three core platforms: transcutaneous monitoring, intrapulmonary percussive ventilation, and electrical impedance tomography.Recognized as a Top Company by Kununu in 2025 and 2026, Sentec values excellence and innovation.

Become a pivotal member of our innovative team as a Senior Embedded Software EngineerSentec AG is a distinguished Swiss-American company at the forefront of medical device technology, specializing in advanced respiratory care solutions. Since our inception in 1999, we have embraced a deep-tech philosophy, integrating cutting-edge science and innovative technologies to enhance the lives of respiratory patients around the globe.Our mission is to drive transformative changes in clinical practices that mitigate the challenges faced by respiratory patients, optimize healthcare outcomes, and reduce costs. We leverage the latest scientific advancements and engineering technologies across our three primary platforms: transcutaneous monitoring, intrapulmonary percussive ventilation, and electrical impedance tomography. All our products are developed and manufactured in-house, ensuring the highest quality standards.We are proud to have received Kununu’s Top Company award in 2025 and 2026.