Regulatory Affairs Technician

Solutia Life Sciences (recruitment division of Solutia) specializes in technical and middle management profiles in the pharmaceutical, biotech, and medical device sectors.

We 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 .

Key Responsibilities :

• Preparation of required technical dossiers and documentation for the registration of medical devices and food supplements.
• Registration 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.
• Requesting Free Sale Certificates for products.
• Continuous communication and assistance to help clients register products in third countries.
• Providing technical support to the QA department, reviewing and approving product labeling according to regulations, and evaluating promotional materials from the marketing department.

Skills :

• Responsible, organized, and proactive.
• Strong communication skills and a team player.
• Advanced level of English (C1).
• Native or fluent in Spanish.
• Proficient in Microsoft Office.

Offered Conditions :

• Permanent contract.
• Monday to Thursday, 8 : 00 AM to 5 : 30 PM, and Fridays from 8 : 00 AM to 2 : 30 PM.

Benefits :

• Continuous training on the job and in-company language courses.
• Life insurance for the employee.
• Affordable catering delivery, fresh fruit every week, and access to an on-site fitness room.

Requirements :

• Bachelor's degree in sciences (biology, nutrition, chemistry, biochemistry, pharmacy, or related fields).
• Preferred : Masters in Regulatory Affairs.
• 1-2 years of experience in a similar role.