Sr. Associate, Regulatory Operations

About the role

Alcon is seeking a Sr. Associate in Regulatory Operations to support its Quality & Regulatory Affairs function. You will work on compliance activities such as Change Control, Audit Management, and Quality Metrics while ensuring regulatory documents meet audit schedules and regulations.

Key responsibilities

• Perform specialized tasks and independent research to optimize outcomes for medical device and pharmaceutical products.
• Prepare dossiers for new registrations, changes, renewals, and promotional material submissions.
• Maintain up‑to‑date databases of submissions and approvals.
• Make decisions within the scope of assigned tasks to achieve project goals.
• Apply advanced analytical skills and self‑direction while adhering to GxP regulations.
• Follow Standard Operating Procedures, maintain accurate documentation, ensure quality control, and complete required training.
• Contribute to overall organizational compliance and continuous improvement.

Required profile

• Bachelor’s degree or equivalent experience.
• Minimum 2 years of relevant regulatory or quality experience.
• Fluent reading, writing, and communication skills in English.

Required skills

• Regulatory dossier preparation for medical devices and pharmaceuticals.
• GxP compliance and SOP adherence.
• Change control and audit management.
• Database maintenance of submissions and approvals.
• Analytical and self‑directed work style.