Validation Engineer - Pharmaceutical and Medical Devices

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.

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.

Join Bosch Group as a Test and Validation Engineer Intern and immerse yourself in the world of cutting-edge technology. This internship provides a unique opportunity to work alongside experienced professionals while contributing to innovative projects that shape the future of automotive technology.

Role Overview Bosch Group is hiring a Test & Validation Engineer focused on SiC Semiconductor Modules in Budapest. This position centers on designing, running, and analyzing tests to confirm the quality and reliability of advanced semiconductor products. What You Will Do Develop and execute test plans for SiC semiconductor modules Analyze test results to identify trends and ensure product reliability Work with cross-functional teams to improve product performance Support the development of new semiconductor technologies Collaboration This role involves close cooperation with colleagues from different disciplines to strengthen product quality and drive innovation in next-generation technologies.

Join our team at Bosch Group as a Lifetime Validation Intern and gain hands-on experience in a dynamic environment. This internship offers a unique opportunity to contribute to our innovative projects while enhancing your professional skills.

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 Bosch Group as a Validation Project Management Intern in Budapest, where you will have the opportunity to work alongside experienced professionals. This internship will provide you with hands-on experience in project management within a global company known for its innovation and quality.Your role will involve assisting in the planning and execution of validation projects, collaborating with cross-functional teams, and contributing to the continuous improvement of processes.

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.

About the Role Bosch Group is looking for a Test & Validation Technician focused on SiC Semiconductor Modules in Budapest. This role centers on hands-on testing and validation to maintain high quality standards for semiconductor products. What You Will Do Carry out thorough testing and validation of SiC semiconductor modules Document results and report findings to the engineering team Support ongoing projects by applying technical skills in laboratory and production settings What We Look For Technical background in electronics, semiconductors, or a related field Experience with testing and validation processes is a plus Attention to detail and commitment to quality Location This position is based in Budapest.

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

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.

SEON Technologies Ltd. develops a command center platform for fraud prevention and AML compliance, used by thousands of businesses worldwide. The platform analyzes over 900 real-time, first-party data signals to enhance customer profiles, detect suspicious activities, and simplify compliance tasks. SEON's technology is trusted by companies such as Revolut, Wise, and Bilt to reduce fraud and manage risk. Role overview This Senior Software Architect role is part of the Architecture team and reports to the VP of Architecture. The position works closely with both the AML and device intelligence engineering teams, with an emphasis on anti-money laundering systems. Responsibilities include contributing to product research feasibility and shaping the technical direction for these areas. Main focus areas Designing solutions that handle high-volume event processing Supporting real-time monitoring of entities Ensuring compliance with regulations in multiple jurisdictions Solving large-scale device fingerprinting challenges Location This position is based in Budapest.

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 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.

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.

Role Overview AbbVie Inc. is hiring an Oncology Medical Advisor in Budapest. This role focuses on supporting cancer treatment by working closely with healthcare professionals and internal teams. The Medical Advisor helps guide clinical strategies and contributes to research efforts that advance oncology care. What You Will Do Collaborate with healthcare professionals to share scientific insights and gather feedback on oncology products. Contribute to the development and execution of clinical strategies for cancer therapies. Support research initiatives aimed at improving treatment pathways and patient outcomes. Ensure oncology products meet high standards for efficacy and safety. Impact Your medical expertise will help shape treatment approaches and improve the quality of care for patients with cancer.

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.

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

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