Regulatory Affairs Trainee

Alcon MX

Cornellà de Llobregat

Presencial

EUR 20.000 - 28.000

Jornada completa

Hace 3 días
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Descripción de la vacante

Alcon is seeking a Regulatory Affairs Trainee in Spain to support regulatory activities for Medical Devices and Medicinal Products. You will assist in AEMPS notifications, prepare tender documentation, coordinate labeling translations, and review labeling for Surgical and Vision Care products.

The role requires pursuing or recently completed Master’s in Pharmacy or Life Sciences, with an advantage for CESIF background and strong English skills.

Formación

  • Currently pursuing or recently completed a Master’s or postgraduate degree in Pharmacy or Life Sciences.
  • A CESIF Master’s in Pharmaceutical Industry would be advantageous.
  • Fluent English (written and spoken)

Responsabilidades

  • Support Spanish Agency of Medicines and Medical Devices (AEMPS) notifications and registrations.
  • Collect and prepare regulatory documentation for Medical Devices and Medicinal Products for tender submissions.
  • Coordinate translation of Medical Device labeling materials.
  • Review Medical Device labeling for Surgical and Vision Care portfolios.
  • Support post-approval regulatory activities for Medicinal Products, notably variations.

Conocimientos

Initiative
Integrity
Teamwork
Results orientation
Planning
Adaptability
Collaboration
English Proficiency

Educación

Master’s in Pharmacy
Health/Life Sciences
CESIF Master advantage

Herramientas

Descripción del empleo

At Alcon, we are driven by the meaningful work we do to help people see brilliantly. As a global leader in eye care, we innovate boldly, champion progress, and act with speed. Here, you will be recognized for your dedication and contributions, and you will gain a vision of your career unlike anything you have experienced before. Together, we go above and beyond to make a meaningful impact on the lives of our patients and customers. We foster an inclusive culture and are looking for diverse and talented individuals to join Alcon.

Key responsabilities: The Regulatory Affairs Trainee will support the Regulatory Affairs team in the following activities:
  • Support Medical Device notification and registration activities with the Spanish Agency of Medicines and Medical Devices (AEMPS).
  • Collect and prepare regulatory documentation for Medical Devices and Medicinal Products required for tender submissions.
  • Coordinate the translation of Medical Device labeling materials.
  • Review Medical Device labeling for the Surgical and Vision Care product portfolios.
  • Support post-approval regulatory activities for Medicinal Products, mainly related to variations.
Key competencies: We are looking for a candidate who demonstrates:
  • Initiative and proactivity.
  • Integrity and trust.
  • Teamwork.
  • Results orientation.
  • Planning and alignment skills.
  • Adaptability.
  • Cooperation and collaboration.
  • Good written and spoken English.
Education & Qualifications:
  • Currently pursuing or recently completed a Master’s or postgraduate degree in Pharmacy or another Health/Life Sciences discipline, such as Chemistry or Biology.
  • A postgraduate or Master’s degree in the Pharmaceutical Industry, particularly the CESIF Master’s program, would be considered an advantage.

At Alcon, we are committed to helping people see better. We believe patients should have access to quality eye care regardless of their economic circumstances; however, barriers to good eye health exist for patients in both developed and emerging markets. Alcon develops and manufactures innovative devices to serve the full life cycle of eye care needs. Its surgical group is one of the largest makers of equipment used for cataract removal and laser vision correction. Its consumer products include the well‑known Opti‑Free line of contact lens solutions and related products. Alcon, which was founded in 1945, sells its products in 180 countries worldwide.

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