As an intern, you will assist the Compliance team in getting new Alcon products approved for sale in new countries. This involves preparing documents, updating records, and helping with various compliance tasks.
Learning Outcomes:
Technical Skills Development: Gain an understanding of the medical device registration process in new markets Learn how to prepare documentation that meet regulatory requirements for product registration Become familiar with Common Product Data Sheets (CPDS) – learn to review and update CPDS to meet pharmaceutical industry standards
Practical Experience: Develop strong organizational and documentation skills to maintain tracking charts for registrations and compliance activities Learn to follow established processes and procedures in a compliance environment Gain exposure to day-to-day operations of a compliance team in the pharmaceutical industry Develop an appreciation for the importance of compliance in bringing safe and effective products to market
Team Collaboration: Build professional relationships and learn to work collaboratively within a team
Document Preparation, Common Product Data Sheets (CPDS) Review and Update
Objective: Ensure that all supporting documents meet regulatory standards and are submitted on time.
Tracking Chart Maintenance
Objective: Monitor the status of product registrations and compliance activities.
Support Compliance Operations
Objective: Actively participate in team operations within a compliance team, gain exposure and understanding of the day-to-day activities and responsibilities of a compliance team in a pharmaceutical manufacturing site
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.