Regulatory Affairs Trainee

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.

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