Join a dynamic global team as a Regulatory Publishing Officer, focusing on compliance and quality in electronic submission formats. Drive successful regulatory submissions across multiple regions and formats.
In this role, you will support regulatory submission publishing activities in various formats, including eCTD and NeeS. With over three years of experience in Regulatory Affairs, you will compile and validate submissions internationally, working collaboratively with internal stakeholders to meet health authority requirements.
Key Responsibilities:
• Perform publishing activities in eCTD, NeeS, ePaper, and ACTD
• Support submissions across the EU, US, Canada, and Australia
• Compile and validate regulatory submissions for health authorities
• Ensure compliance and accuracy of published documents
• Plan and coordinate publishing projects with stakeholders
Requirements:
• Bachelor’s degree in Life Sciences or related field
• 3+ years in Regulatory Affair...