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Solutia Life Sciences, a recruitment division specializing in technical and middle management profiles, is seeking a Regulatory Affairs Technician for a pharmaceutical company in the oncology products and high-potency drugs sector.
Key Responsibilities:
- Prepare technical dossiers and documentation for medical device registration.
- Register medical devices with AEMPS and food supplements with the Public Health Department of Generalitat de Catalunya.
- Request Free Sale Certificates for products.
- Provide technical support to QA departments, reviewing product labeling, and evaluating promotional materials.
Skills:
- Responsible, organized, and proactive individual.
- Strong communication skills and team player.
- Advanced level of English (C1).
- Native or fluent in Spanish.
- Proficient in Microsoft Office.
Offered Conditions:
- Permanent contract.
- Flexible working hours.
- Continuous training and in-company language courses.
- Life insurance and benefits package.
Requirements:
- Bachelor's degree in sciences (biology, nutrition, chemistry, biochemistry, pharmacy, or related fields).
- Prior experience in regulatory affairs.