About this role
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.
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