A leading medical technology company is seeking a Regulatory Specialist in San Agustin del Guadalix, Spain. The role involves ensuring compliance with industry standards and conducting regulatory activities for multiple projects. Responsibilities include reviewing promotional materials, managing regulatory documentation, and supporting CE marking initiatives. The ideal candidate should possess a degree in Life Sciences and have 3-5 years of regulatory affairs experience in the medical device sector. Opportunities for professional growth and meaningful contributions are available. #J-18808-Ljbffr