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.