Associate - Regulatory Affairs (Publishing)

Added
less than a minute ago
Type
Contract
Salary
Salary not provided

Related skills

microsoft office veeva vault ectd lorenz docubridge pdf_optimization

๐Ÿ“‹ Description

  • Support preparation of eCTD and non-eCTD submissions.
  • Format documents, hyperlink, bookmark, and optimize PDFs.
  • Assist in submission compilation and publishing.
  • Conduct technical validation checks prior to submission.
  • Maintain submission trackers and documentation logs.
  • Ensure metadata accuracy and correct document placement.

๐ŸŽฏ Requirements

  • Bachelorโ€™s degree (Life Sciences / Pharmacy / Biotechnology preferred).
  • 0โ€“1 year experience (freshers may apply).
  • Basic understanding of pharmaceutical regulatory environment.
  • Good knowledge of MS Office (Word, Excel, PowerPoint).
  • Strong attention to detail.
  • Familiarity with publishing tools (eCTD tools, Veeva Vault, Lorenz DocuBridge).
  • Time management and ability to meet deadlines.
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