Sobre este puesto de Regulatory Affairs Trainee en Alcon
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: Current Alcon Employee/Contingent Worker
If you are currently an active employee/contingent worker at Alcon, please click the appropriate link below to apply on the Internal Career site.
