Associate Ii Regulatory Operations

Alcon

Veeva rim publishing tools
Electronic submissions
Regulatory validators
Prepare, compile, and publish regulatory submission dossiers for global markets (US, EU, RoW)

Job Summary

  • Prepare, compile, and publish regulatory submission dossiers for global markets (US, EU, RoW).
  • Perform publishing activities for eCTD, NeeS, and paper submissions in accordance with regional regulatory guidelines.
  • Support submission readiness, publishing timelines, and coordination with Regulatory Affairs and cross-functional teams.

Matching Summary

Prepare, compile, and publish regulatory submission dossiers for global markets (US, EU, RoW).

Skills & Requirements

Must-have

  • Veeva RIM Publishing tools
  • electronic submissions
  • regulatory validators
  • eCTD, NeeS, and paper submissions
  • global regulatory markets

Nice-to-have

  • process improvements
  • inspection readiness
  • audit support activities

Key Requirements

  • 3–4 years of experience
  • Bachelor’s degree in Pharmacy, Life Sciences, or related
  • Hands-on expertise with Veeva RIM Publishing
  • Experience with regulatory validators
  • Understanding of eCTD structure

Work Rights

Not specified

Tailored Resume

Cover Letter