R&D

(Senior) R&D Engineer (m/f/d) Location: Mainz, Germany (Hybrid) Overview: This company is one of the leading developers and manufacturers of medical devices and aids for patients. The premium product portfolio focuses on patient care in the clinic and in the homecare sector. The company has a 60-year history and has already been voted into the top 100 German SMEs three times. Benefits:   Attractive Remuneration: Benefit from a competitive package that reflects your skills and contributions and generously rewards your hard work. Annual pay reviews are to be expected. Flexible Work Options: Take advantage of the opportunity to work from home 2 days per week after your probation period Generous Vacation Policy: 30-days’ vacation. Recharge and rejuvenate, giving you ample time to relax and enjoy life outside work. Health-Management Program: To make sure employees find the right balance between work and everyday life (running groups, yoga, burnt-out prevention, and various other strategies) + access to a discount website covering a wide range of services/partners Permanent Full-Time Position: Permanent employment in a growing company with secure future prospects. Continuous Evolution & Development: Wide range of development opportunities, including the possibility of team leadership Responsible and varied tasks working in a fun and diverse team Team Events; benefit from being part of a wider global operation with summer and winter company events. Tasks:   You work on development projects for passive medical products made of plastics - from conception, design, and prototypes to series production for clinical application You create the relevant technical development documentation in accordance with regulatory requirements (e.g. DIN EN ISO 13485, MDR, CFR820) You work on technical concepts, realisation in 3D CAD, prototypes and verification and validation measures Your Profile:   You have a completed engineering degree with a focus on plastics technology or medical technology or comparable qualifications You have several years of practical experience in managing projects 5 + years of professional experience in R&D for Medical Technology with a focus on plastics components In addition to technical know-how, you have good analytical and methodological skills as well as a structured, solution- and result-oriented way of working You enjoy working in a team and impress with your communication skills, enthusiasm, motivation and conflict-resolution skills You have very good German and fluent English skills, both written and spoken Experience working in an international environment To apply or for more information, please get in touch with Luke Fines by email with a copy of your CV at: luke.fines@adaptivelifescience.com           

Instructional Designer (Digital Training) Location: Hamburg area (hybrid flexibility) Are you an innovative Instructional Designer with expertise in digital training media? Do you excel in Articulate Storyline, Adobe CC, and H5P to create engaging and high-quality digital learning experiences? Our client, a global leader in healthcare diagnostics, is renowned for its groundbreaking products and dedication to enhancing the healthcare journey. They’re currently seeking an International Instructional Designer to join their digital training team and make a significant impact in advanced e-learning development. Main responsibilities: Develop, design, and produce engaging digital training content for medical diagnostics and healthcare topics Create and integrate graphics, animations, videos, and interactive elements into training modules Lead digital training project management, from conceptualization to release, ensuring high-quality output Collaborate with international instructional design experts to refine and innovate training solutions Continually improve workflows to maintain and elevate the quality of training media produced What is required: Advanced skills in digital training development with expertise in web-based training using Articulate Storyline. Strong graphic design skills with Adobe Photoshop, Illustrator, and After Effects, along with basic video production and post-production experience. Solid experience in technical and scientific storytelling, with resourceful communication skills to collaborate effectively with SMEs. Experienced in planning and coordinating training media productions. Adaptable and quick learner, open to continuous skill growth and enthusiastic about contributing to an international, intercultural team. 3D design skills with tools like 3DS Max, Cinema 4D, or Blender would be an advantage. Fluency in English (written and spoken). Willingness to travel globally (up to 30%). What is offered: Assistance for relocation to the Hamburg area. Hybrid working model with 30 days of annual leave. Broad learning and development opportunities, including access to an on-site training campus. Christmas and holiday bonuses, childcare support, subsidized pension plan, company discounts, and canteen lunch subsidies. In-house gym, sports courses, massages, psychological support, and general health management services Public transport subsidy, bike leasing options, and free parking. If you enjoy leading your own projects, collaborating with subject-matter experts, and working within a dynamic, international team, this opportunity may be a perfect fit! Who Are Adaptive Life Science? Here at Adaptive Life Science, we provide specialised recruitment services to the Life Science sector, covering the Medical Device, Diagnostic, and Biotech industries globally. We are connected with the most innovative medical companies in the world, and are ready to support your career development with them. Why Apply With Us? Our services are 100% free to candidates, and our focus is helping you find your dream job that aligns with your career goals, technical skill set, and culture fit. We offer a range of services, including: Expert advice on your CV and cover letter Guidance on salary expectations Personalized interview preparation Connections to exclusive job opportunities Assistance in negotiating the best possible offers 50% of the CVs we send to clients are accepted Accepted or declined, either way we will provide you with feedback We believe in being your trusted advisor throughout your job search. We will take the stress out of the process by working around your schedule, and with your needs. Who Do Adaptive Work With? We offer a wide portfolio of over 150+ Life Science companies, from start-ups with impressive funding and innovative product development, mid-sized companies investing in R&D, all the way to market leaders with significant global presence. If you are interested in this role, please apply with your CV or contact Dominika Wyrwinska for further details on this opportunity and additional vacancies in the medical device, biotech, and diagnostics industry. dominika.wyrwinska@adaptivelifescience.com #LI-DW1 #LI-Hybrid

Are you passionate about ensuring safety and quality?   Do you enjoy navigating regulatory standards and managing product compliance?   Join our innovative client and play a crucial role in ensuring their devices meet all regulatory requirements and safety standards.   This position is ideal for someone with an engineering background, with a solid understanding of regulatory requirements who thrives in a detail-oriented, cross-functional environment!   Key Responsibilities: Identify and interpret compliance standards for our products. Assess standard updates and determine necessary adjustments with relevant departments. Develop product specifications for new products based on industry standards. Oversee approvals and maintain certifications by collaborating with both internal teams and external authorities. Work closely with certification agencies (e.g., UL, TÜV) to meet industry requirements. Plan, coordinate, and conduct risk assessments for our medical devices (including electronic components and software). Support product development in defining and validating risk-reducing measures. Schedule and perform routine reviews of risk assessments.   Requirements: Bachelor's degree in Engineering e.g. Electrical Engineering or equivalent technical training with relevant professional experience. Familiarity with regulatory requirements for medical devices or electronic appliances. Excellent communicator and team player who enjoys interfacing between development and regulatory compliance. Fluency in German and English.   If you're interested in this position, please apply and/or contact Hollie Dear at Adaptive Life Science for more information.

Are you an accomplished Senior Software Architect looking for your next challenge? Do you want to lead the design and development of ground-breaking software solutions for innovative medical devices? Join a leading MedTech company and play a pivotal role in shaping the future of healthcare technology! Key Responsibilities: Lead the design and architecture of complex software systems for medical devices, ensuring they meet industry standards and regulatory requirements (e.g., FDA, ISO 13485). Collaborate with cross-functional teams, including product management, hardware engineering, and quality assurance, to define system requirements and architecture specifications. Develop and maintain software architecture documentation, ensuring clear communication of architectural decisions and design rationale. Drive continuous improvement in software development practices, including design patterns, coding standards, and best practices for scalability, security, and performance. Mentor and guide junior software engineers, fostering a culture of innovation and technical excellence within the team. Perform risk assessments and implement mitigation strategies to ensure product safety and compliance. Oversee the integration of third-party tools and technologies, ensuring seamless compatibility with existing systems. Collaborate with regulatory and quality teams to support validation and verification activities for software components. Ensure software systems are maintainable, modular, and adaptable to future product enhancements and evolving market needs. Lead technical discussions and decision-making processes, balancing long-term architectural goals with short-term project deadlines. Requirements: Bachelor's or Master's degree in Computer Science, Software Engineering, or related field. Minimum of 5 years of experience in software engineering, with at least 3 years in a senior or lead architectural role, preferably within the medical device industry (or a regulated industry). Strong experience with embedded systems, real-time operating systems, and software development lifecycle in a regulated environment. Expertise in software design principles, architectural patterns, and scalable system design. Proficiency in programming languages such as C++,  Python, JSON and experience with embedded programming. Knowledge of software testing, debugging, and profiling tools. Strong understanding of security, data integrity, and privacy in medical device software. Familiarity with industry standards and regulatory requirements (FDA, IEC 62304, ISO 14971) is preferable.  Excellent communication and leadership skills, with a track record of collaborating effectively across teams. Fluency in German and English.    If you're interested in this position, please apply and/or contact Hollie Dear at Adaptive Life Science for more information.

Looking for your next challenge in Embedded Systems Engineering?   Passionate about driving innovation in cardiovascular healthcare?   Join our client in Berlin and be a key part of their mission to make a real impact!   Key Responsibilities: Oversee the design, development, and refinement of embedded systems for medical devices, ensuring top-tier reliability, safety, and efficiency • Create and manage embedded firmware and software, including low-level device drivers, real-time operating systems, and communication protocols • Conduct system analysis and debugging to diagnose and resolve intricate issues in embedded systems • Assist in the preparation and review of technical documents such as design specifications, test plans, and user guides • Ensure adherence to medical device regulations, including FDA, ISO, and other industry standards • Perform code reviews and provide technical guidance to junior engineers • Collaborate with cross-functional teams to outline system requirements and ensure they align with project goals • Ensure successful system development and delivery by balancing technical needs, resources, and stakeholder expectations throughout the project’s life cycle • Recruit and manage a team of developers, including both freelancers and full-time employees • Stay informed about emerging technologies and industry trends to enhance existing systems and explore new opportunities   Requirements: A degree in Electronics, Electrical Engineering, or a related field. 7+ years of experience in embedded systems engineering, with significant exposure to medical device development (or another regulated industry) Skilled in embedded C/C++ programming with hands-on experience in real-time operating systems (RTOS) and Linux Strong knowledge of hardware-software integration, including working with microcontrollers, sensors, and communication interfaces Experience with version control tools (e.g., Git) and development environments, including IDEs, debuggers, and CI/CD automation Excellent communication and teamwork skills, capable of working in a multidisciplinary environment Knowledgeable about medical device regulations and standards, such as IEC 62304 and ISO 13485 Experience with safety-critical systems and software development life cycle (SDLC) methodologies is essential     If you're interested in this position, please apply and/or contact Hollie Dear at Adaptive Life Science for more information.

Development Engineer  We are supporting an innovative client located near Nuremberg, specializing in the field of endoscopic medical devices, in their search for a Development Engineer. This role focuses on the development and optimization of advanced medical products and offers an exciting opportunity to contribute directly to the future of healthcare. The tasks: Lead the development of new and innovative single-use medical products within a structured product development process. Support the creation and maintenance of essential product documentation in compliance with MDR regulations. Plan, conduct, and analyze tests and trials to support ongoing development efforts. Collaborate in the further development and optimization of existing products, components, and manufacturing processes. Your Profile: A Degree in Engineering and experience in product development, particularly with single-use medical devices. Strong knowledge of plastic components and current technologies relevant to the medical device industry. Familiarity with relevant standards and regulatory requirements. Proficiency in CAD software, such as SolidWorks, and excellent project management skills. Strong communication skills in English and German, both written and spoken. Advanced user knowledge of Microsoft Office (Word, Excel, PowerPoint). What’s on Offer: A long-term position in a growing company within the healthcare sector. Responsible and varied tasks with opportunities for professional development. Opportunities for growth through internal and external training. Competitive benefits package, including a company pension scheme and health perks   Who Are Adaptive Life Science? Here at Adaptive Life Science, we provide specialised recruitment services to the Life Science sector, covering the Medical Device, Diagnostic, and Biotech industries globally. We are connected with the most innovative medical companies in the world, and are ready to support your career development with them.   Why Apply With Us? Our services are 100% free to candidates, and our focus is helping you find your dream job that aligns with your career goals, technical skill set, and culture fit. We offer a range of services, including: Expert advice on your CV and cover letter Guidance on salary expectations Personalized interview preparation Connections to exclusive job opportunities Assistance in negotiating the best possible offers 50% of the CVs we send to clients are accepted Accepted or declined, either way we will provide you with feedback We believe in being your trusted advisor throughout your job search. We will take the stress out of the process by working around your schedule, and with your needs. Who Do Adaptive Work With? We offer a wide portfolio of over 150+ Life Science companies, from start-ups with impressive funding and innovative product development, mid-sized companies investing in R&D, all the way to market leaders with significant global presence. If you are interested in this role, please apply with your CV or contact Dominika Wyrwinska for further details on this opportunity and additional vacancies in the medical device, biotech, and diagnostics industry.   dominika.wyrwinska@adaptivelifescience.com #LI-DW1

Are you a seasoned Software Engineer, ready for a new challenge? Would you like to join an international medical device company who are producing life-saving devices? Are you passionate about leadership and guiding your team through every phase of the development? Our client in the medical device industry are looking to strengthen their team and searching for a Senior Manager in Software Engineering to join them!   Responsibilities:   Leadership and Team Support: Provide disciplinary leadership and support to the team, focusing on fostering self-organization and coaching in all technical and technological challenges. Development Environment Improvement: Actively participate in the continuous enhancement of the development environment, including processes, tools, and their practical applications. Software Quality Enhancement: Contribute to the ongoing improvement of software, software architecture, and software quality. Resource Management: Assist with personnel planning and resource allocation per project as needed. Process Compliance: Ensure adherence to development processes and standards. Strategic Implementation: Actively implement the overall corporate strategy. Guideline Development: Further develop internal guidelines and quality standards for the development process. External Coordination: Coordinate and develop external partners and service providers.   Requirements and Skills: Educational Background: Completed studies in computer science, electrical engineering, physics, medical technology, or a comparable field. Management Experience: Proven experience in employee development, goal setting, and coaching. Technical Expertise: Several years of experience in software development, preferably in embedded software development, with solid programming knowledge in C/C++. Agile Environment: Experience working in an agile environment. Professional Experience: Minimum of 5 years of professional experience in development, preferably for medical devices. Language Skills: Fluent English with a good level of German or a willingness to take German courses. Travel Willingness: Willingness to travel occasionally, both nationally and internationally.   Benefits Mobile Work: The possibility to work remotely. Impactful Work: Whether in front of or behind the scenes, you will contribute to making better medicine available to more and more people worldwide. Career Development: Individual opportunities for self-determined career planning and professional growth. Innovative Culture: A corporate culture that encourages innovative thinking to find the best, not just the fastest, solutions together. Diverse Team: A large number of committed people with a wide range of skills, talents, and experiences. Corporate Benefits: Enjoy the benefits of a successful global corporation combined with the collegial culture of a medium-sized company.   If you're interested in this position, please apply here and/or contact Hollie Dear at Adaptive Life Science for more information.