Solutia Life Sciences (recruitment division of Solutia) specializes in technical and middle management profiles in the pharmaceutical, biotech, and medical device sectors.
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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 .
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Key Responsibilities
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- 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:\n
- 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:\n
- Permanent contract.
- Monday to Thursday, 8:00 AM to 5:30 PM, and Fridays from 8:00 AM to 2:30 PM.
Benefits:\n
- 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:\n
- 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.