Regulatory Affairs Technician

hace 4 semanas


Barcelona, Barcelona, España Solutiaghs A tiempo completo

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: Master's in Regulatory Affairs.
  • 1-2 year of experience in a similar role.


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