Senior Associate - Regulatory Affairs

📋 Description

• Support preparation of eCTD and non-eCTD submissions
• Perform document formatting, hyperlinking, bookmarking, and PDF optimization
• Assist in submission compilation and publishing activities
• Conduct technical validation checks prior to submission
• Maintain submission trackers and documentation logs
• Ensure metadata accuracy and correct document placement

🎯 Requirements

• Bachelor’s degree (Life Sciences / Pharmacy / Biotechnology preferred)
• 3–5 years of experience
• Basic understanding of pharmaceutical regulatory environment (preferred but not mandatory)
• Good knowledge of MS Office (Word, Excel, PowerPoint)
• Strong attention to detail
• Good written and verbal communication skills