Connecting World Class Talent With The Most Innovative Medical Companies

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 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  

Are you an experienced ReactJS Developer, searching for your next challenge? Join an innovative tech company who are utilising advanced technologies to support some of the world’s leading medical device and pharmaceutical companies. Responsibilities:   Craft compelling, user-friendly interfaces through ReactJS, translating design concepts into dynamic, responsive features. Create rapid prototypes and proof of concept using ReactJS libraries, facilitating swift iteration and validation. Transform approved prototypes into robust web applications, adhering to security, performance, and maintainability standards throughout the development lifecycle. Drive the development, testing, deployment, and maintenance of the front-end for a SaaS solution. Fine-tune web components for optimal performance across diverse browsers, ensuring seamless user experiences. Facilitate seamless integration between front-end and backend through Restful services, supporting the overall functionality of the application. Experience required: More than five years of expertise designing and developing Web User Interface frameworks with front-end JavaScript technologies. Proficiency with HTML5 Image rendering (Canvas, SVG, etc.) and React technologies (React.js, Webpack, Redux, etc.) Working knowledge of front-end languages, JavaScript, CSS, HTML5, JSON, and HTTP/AJAX. Proficiency with browser-based debugging and performance testing technologies, as well as performance testing frameworks like Mocha, Jest, and Selenium. Fluent English is required. If you're interested in this position, please apply here and/or contact Hollie Dear. #LI-HB1  #LI-Hybrid

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