Solutia Life Sciences (recruitment division of Solutia) specializes in technical and middle management profiles in the pharmaceutical, biotech, and medical device sectors. brWe are currently selecting a Regulatory Affairs Technician for a pharmaceutical company specialized in the development and production of innovative oncology products and high-potency drugs located in Vallès Occidental. brKey Responsibilities: brPreparation of required technical dossiers and documentation for the registration of medical devices and food supplements. brRegistration of medical devices with the Spanish Agency of Medicines and Medical Devices (AEMPS) and food supplements with the Public Health Department of the Generalitat de Catalunya. brRequesting Free Sale Certificates for products. brContinuous communication and assistance to help clients register products in third countries. brProviding technical support to the QA department, reviewing and approving product labeling according to regulations, and evaluating promotional materials from the marketing department. Skills: brResponsible, organized, and proactive. brStrong communication skills and a team player. brAdvanced level of English (C1). brNative or fluent in Spanish. brProficient in Microsoft Office. Offered Conditions: brPermanent contract. brMonday to Thursday, 8:00 AM to 5:30 PM, and Fridays from 8:00 AM to 2:30 PM. Benefits: brContinuous training on the job and in-company language courses. brLife insurance for the employee. brAffordable catering delivery, fresh fruit every week, and access to an on-site fitness room. Requirements: brBachelor's degree in sciences (biology, nutrition, chemistry, biochemistry, pharmacy, or related fields). brPreferred: Masters in Regulatory Affairs. br1-2 years of experience in a similar role.