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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