Prepare and manage BLA (Biologics License Application) submissions in eCTD format using Veeva Vault eCTD Publishing.
Hands-on experience with Docubridge and Lorenz Validator for regulatory submissions.
Strong background in Regulatory Publishing with knowledge of global regulatory requirements (FDA, EMA) .
Experience in Life Sciences / Pharma regulatory publishing .
Proficient in Adobe Acrobat Pro and Microsoft Office Suite .
Skilled in working with GDMS / Mediva for document management.
Experienced in collaboration tools such as SharePoint and Communicator .
Veeva Etcd Publisher • Hyderabad, India