Regulatory Affairs Trainee

Job description

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.

ATTENTION

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