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Development Engineer (m/f/d) Location: Elmshorn, Germany| Largely onsite Overview: This company is a distinguished, owner-managed medical technology firm based in Elmshorn, located north of Hamburg, Germany. With a rich history spanning over 75 years, this company has established itself as a leader in the development and production of high-quality medical products that are exported to markets around the globe. Benefits: Crisis-Proof Job: Enjoy job security and stability even in uncertain economic times, ensuring peace of mind for you and your family. Attractive Remuneration: Benefit from a competitive salary package that reflects your skills and contributions, rewarding you generously for your hard work. Flexible Work Options: Take advantage of the opportunity to work from home 1-2 days per week, offering a perfect balance between professional productivity and personal comfort. Generous Vacation Policy: Recharge and rejuvenate with 30 days of vacation per year, giving you ample time to relax and enjoy life outside of work. Permanent Full-Time Position: Secure a long-term career with a full-time position that offers stability, growth, and the potential to advance within the company. Continuous Learning and Development: Enhance your skills and knowledge through regular training and further education opportunities, fostering your personal and professional growth. Monthly Benefits: Enjoy a monthly fuel voucher or, if you prefer, a shopping voucher to help with everyday expenses and add a little extra to your monthly budget. Convenient Location: Benefit from good accessibility and free parking, making your daily commute hassle-free and convenient. Engaging Corporate Events: Connect with colleagues and build strong team relationships through regular corporate events, fostering a positive and collaborative work environment. Tasks: Lead the development of new products and the enhancement of existing ones, acting as the innovator for system architecture and concepts. Oversee requirements management and associated definitions. Create 3D CAD models, perform FEM simulations, and conduct drawing reviews. Collaborate closely with product management. Facilitate the transition of designs to production. Provide technical support to customer service. Prepare and document technical tests. Your Profile: A university degree in Electrical Engineering, Mechanical Engineering, Mechatronics, or a related field Alternatively, 3-5 years of professional experience as a Development or Systems Engineer Advanced proficiency in 3D CAD tools, preferably AUTODESK Inventor Experience in project management or project conception Expertise in system development and requirements engineering Proficiency in both German and English Residency in Germany with a willingness to relocate to the greater Hamburg area, if applicable A genuine passion for technology! To apply or for more information please contact Luke via email on: luke.fines@adaptivelifescience.com                #LI-Hybrid #LI-LF1

Head of Global Regulatory Affairs   Are you an experienced Regulatory Affairs professional who is passionate about utilizing AI to make a global impact in healthcare? Our Berlin-based client, an innovator in AI-driven diagnostic solutions, is currently looking for a Global Head of Regulatory Affairs. This role offers home office flexibility and the chance to lead a global team as they expand into international markets, including the US. You would oversee compliance, lead two employees, coordinate teams in India and Egypt, and support market access initiatives.   Your tasks:  Design and monitor processes according to ISO 13485 Lead the regulatory development of certified, AI-based medical devices Expand their software to new international markets, including the USA Oversee risk management in accordance with ISO 14971 Support the product team throughout the product lifecycle, and liaise with government agencies to uphold safety and effectiveness. Collaborate on data protection and IT security issues. Your Profile Experience with ISO 13485 for medical devices, preferably in SaMD. Knowledge of MDR, IEC 62304, ISO 14971, etc. +5 years of experience in Regulatory Affairs within medical technology Strong sense of responsibility and organization Excellent communication skills in English and German What is offered: A dynamic, results-oriented work environment with flexible office/home options. Opportunities for skill development through conferences, workshops, and seminars. Regular team events to enhance corporate culture and solidarity. If you're ready to pioneer the future of AI in healthcare, apply now! If you have any questions regarding the position, please contact: Dominika Wyrwinska at dominika.wyrwinska@adaptivelifescience.com #LI-DW1 #LI-Remote

Employee Production Control and Planning   Overview Do you have experience working in Production Control and Planning? Are you looking for a new challenge in the medical device industry? Are you looking for a great company culture that is open-minded, innovative and very future-oriented? Our client near Freiburg who specializes in medical endoscopes is looking for an employee in production control and planning to join their team. Tasks Production and progress control of internal and external delivery including dates and quantity as well as ensure on-time deliveries to customers Coordination of development and sample orders and identify bottlenecks Contact person between departments and other divisions  Analysis of value steams, identification of potentials and implementation of suitable measures   Your profile Completed a commercial or technical vocational training or training in the logistics sector Experience in scheduling or work preparation and knowledge of MS Office High awareness in quality and ability to work under pressure Strong communication and organizational skills Fluency in German and English 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 May-Lynn Capocciama-Knecht for further details on this opportunity and additional vacancies in the medical device, biotech, and diagnostics industry. may-lynn.ck@adaptivelifescience.com +49 30 1663 7750 #25187

Are you searching for your next career step in Software Engineering? Would you like to join an innovative team in the medical device field who are known for their high-tech advancements in the microscopy field? We're currently supporting a client who are headquartered in Innsbruck and are looking to strengthen their team. Responsibilities: Develop and implement software solutions tailored for medical devices, with an emphasis on robotics and imaging technologies. Work closely with the R&D team to create cohesive and integrated solutions. Engage in architectural design and the development process, fostering innovation and improving product performance. Operate within a development environment that adheres to industry standards and regulatory requirements specific to medical technology. Perform code reviews and maintain software to ensure the highest quality standards are met.   Requirements and Skills: Bachelor's degree in Computer Science, Software Engineering, or similar. Proficiency in programming languages such as C++ and Python. Experience working with the Linux operating system. Familiarity with tools like Confluence, Jira, Git, and Continuous Integration (CI). Fluency in English, German is a bonus.   If you're interested in this position, please apply here and/or contact Hollie Dear at Adaptive Life Science for more information. #LI-HB1  #LI-Hybrid  

Are you an experienced Embedded Software Developer, and open for your next career step? Would you like to have an impact on the development of high quality medical devices? Join an innovative medical technology company, who are known globally for their advancements in the endoscopic field. Responsibilities:   Develop embedded software for medical endoscopes, focusing on image processing. Analysis of existing systems to identify optimization opportunities in both software and hardware design. Take charge of software design, architecture, and implementation. Generate specifications and testing strategies for software, ensuring thorough documentation. Translate system requirements into precise software specifications. Collaborate with circuit and FPGA design developers to implement hardware-related application and operating system components (utilizing Linux/Yocto on FPGA). Develop and integrate SoC-specific Board Support Package (BSP) into embedded Linux OS builds. Experience required: Degree in Computer Engineering, Electrical Engineering or comparable. Demonstrated experience in system software development, particularly with Linux/Yocto on FPGA/C/C++ or similar embedded systems. Fundamental grasp of software design and development methodologies. Preferably you will bring experience in a regulated industry (ideally medical technology). Ideally you have familiarity with Xilinx Zynq UltraScale+ MPSoc and its development environment. Fluent German and English is required. If you're interested in this position, please apply here and/or contact Hollie Dear. #LI-HB1  #LI-Hybrid  

Assembly Employee Overview Do you have an optical and/or mechanical background? Are you a detail-oriented person who is experienced working with small parts? Are you looking for a new challenge in the medical device industry? Are you looking for a great company culture that is open-minded, innovative and very future-oriented? Our client near Freiburg who specializes in medical endoscopes is looking for an assembly employee to join their team. Tasks Assembling optical and mechanical assemblies according to technical drawing sna work instructions Document workflows and check for completeness and quality Carry out in-process tests Able to work with specific hand tools and devices   Your profile Technical Vocational Training such as mechanic, technician or similar Experience in manufacturing process with a good technical understanding Precise and structured way of working as well as high quality awareness Expert of complex assembly techniques Fluency in German and English 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 May-Lynn Capocciama-Knecht for further details on this opportunity and additional vacancies in the medical device, biotech, and diagnostics industry. may-lynn.ck@adaptivelifescience.com +49 30 1663 7750 #25114

Product and Process Optimization Engineer Overview Are you an expert in product and process optimization? Are you looking for a new challenge in the medical device industry? Are you looking for a great company culture that is open-minded, innovative and very future-oriented? Our client near Freiburg who specializes in medical endoscopes is looking for a product and process optimization engineer to join their team. Tasks Planning and optimizing work processes in production Support with new product introduction and manufacturing processes Assist in the qualification and validation of systems and manufacturing processes Define and implement suitable measures while processing deviations Develop processes using agile and lean methodologies   Your profile Degree in medical or technical studies or equivalent education Experience in the medical technology or medical device field, ideally in the ISO 13485 regulatory environment Knowledge of agile and lean methodology as well as technical knowledge of manufacturing technologies Good teamwork and communication skills Solutions-oriented and structured Fluency in German and English 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 May-Lynn Capocciama-Knecht for further details on this opportunity and additional vacancies in the medical device, biotech, and diagnostics industry. may-lynn.ck@adaptivelifescience.com +49 30 1663 7750 #25113

Regulatory Affairs Officer Overview Are you looking for a new challenge in regulatory affairs? I am currently supporting a client who specializes in sleep diagnostics in southern Germany in hiring an expert in EU MDR, approval processes, IEC 60601, IEC 62304 and ISO 14971. This is a hybrid working position where you can work 2/3 days from home. Tasks Implementation and maintenance of regulatory approval of medical devices in accordance with EU MDR Assisting in the compilation of documentation and supporting in the creation and maintenance of risk management files in accordance with ISO 14971 and usability files in accordance with IEC 62366-1 Support international distributors in the approval process of the medical devices PMS activities such as PMS files and vigilance investigations Your profile Experience in areas such as regulatory affairs or technical documentation in the MedTech or medical device industry Solid foundational knowledge of relevant regulatory and normative requirements (MDD, MDR, ISO 13485 etc.) IT Skills such as MS Office Good communication and organizational skills as well as independence and reliability Fluency in English and German Please apply with your CV or contact May-Lynn Capocciama-Knecht for further details on this opportunity and additional vacancies in R&D, Regulatory Affairs and Quality Management. may-lynn.ck@adaptivelifescience.com +49 30 1663 7750 #LI-MC2