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 Cerdanyola del Vallès .
Key Responsibilities: Prepare and manage regulatory documentation required for product approval and commercialization.
Ensure compliance with national and international regulations for dietary supplements, medical devices, and cosmetics.
Collaborate with internal teams to coordinate and update technical product documentation.
Stay updated on regulatory changes to ensure continuous product compliance.
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: Master's in Regulatory Affairs.
0-1 year of experience in a similar role.