Regulatory Affairs Specialist – Medical Devices

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998, with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas. We are looking for an experienced Quality Assurance & Regulatory Affairs (QARA)...

Edwards Lifesciences Belgium is seeking a Clinical Quality Specialist to support product quality activities and provide clinical guidance across complaint investigations. You will review complex cases, analyze imaging data, and contribute to regulatory submissions while working with engineers and cross-functional teams. Applicants should have a Bachelor's...

About us INDIBA Group is a global medical device company specializing in radiofrequency and laser technologies for the physiotherapy, aesthetics and veterinary markets. With more than 40 years of scientific research and innovation, our technologies and solutions are used by healthcare professionals worldwide. Through our INDIBA and K-LASER brands, we combine...

About Mira Mira is a San Francisco-based hormonal health company providing integrative care and hormonal testing for over 300,000 customers. In 2023, we were recognized by Inc. 5000 as America's fastest-growing femtech company. About Mira Mira is a San Francisco-based hormonal health company providing integrative care and hormonal testing for over 300,000...

HIPRA is a pharmaceutical and biotechnology company focused on prevention and diagnostics for both animal and human health, offering a broad portfolio of highly innovative vaccines and advanced diagnostic services. The company has a strong international presence in more than 40 countries through its own subsidiaries, 11 diagnostic centres, and 6 production...

Job Description The Senior Regulatory Affairs Specialist is responsible for executing and maintaining EO Hub compliance activities for importers, distributors, and Authorised Representatives in accordance with applicable legislations. The role acts as a subject matter expert for the execution of processes related to device registrations, compliance...

WHY CHOOSE MEDSIR We are a Barcelona-based fastest-growing company founded by scientific experts. We are dedicated to the design and management of innovative strategic clinical trials in oncology, from study conception to the publication of study results. Together, we create the best strategies that are both clinically relevant and scientifically meaningful....

Expansion People busca un/a QA/RA Specialist para liderar Quality & Regulatory Affairs en un proyecto de expansión internacional en el sector Healthcare/Medical Devices. Serás la referencia en cumplimiento regulatorio, gestionando QMS ISO 13485, MDR 2017/745 y documentación técnica, además de coordinar auditorías y colaborar con Producto/I+D. Se...

At Sonova, we envision a world where everyone can enjoy the delight of hearing. This vision inspires us and fuels our commitment to developing innovative solutions that improve hearing health and human connection - from personal audio devices and wireless communication systems to hearing aids and cochlear implants. We're dedicated to providing outstanding...