Lead – Regulatory Publisher

Katalyst HealthCares and Life Sciences

Posted on: April 24, 2026

Closing: May 24, 2026

Salary: Undisclosed

Job Description

Responsibilities:
  • Lead and manage publishing activities for IND, NDA, ANDA, Amendments, Supplements, Responses, Annual Reports, Safety Reports, and Promotional Submissions.
  • Oversee submission-level and document-level publishing including metadata, hyperlinking, bookmarking, TOCs, and lifecycle management.
  • Perform and oversee quality control checks to ensure error-free regulatory submissions.
  • Manage workload allocation, tracking, and timely delivery across teams.
  • Support and mentor team members; conduct training sessions on publishing standards and processes.
  • Handle client communication, status updates, and submission readiness reviews.
  • Manage post-publishing activities including archiving and authority acknowledgements.
  • Contribute to process improvements, automation, and business growth initiatives.
Requirements:
  • Bachelor's or Master's degree in Pharmacy, Life Sciences, or a related discipline.
  • Strong expertise in eCTD/NeeS publishing for US market.
  • Strong expertise knowledge of the Archival process.
  • Hands-on experience with publishing tools such as DocuBridge, EXTEDO eCTD Manager, ISI Toolbox, Adobe Acrobat, and validation tools (Lorenz/eValidator).
  • In-depth knowledge of ICH and regional regulatory submission guidelines.
  • Experience in handling validation errors and troubleshooting technical issues.
  • Strong stakeholder management, communication, and leadership skills.
  • bility to work in fast-paced, changing regulatory environments.
  • Minimum 5 - 10 years' experience for handling submission and Archival.

Katalyst HealthCares and Life Sciences

Posted on: April 24, 2026

Closing: May 24, 2026

Salary: Undisclosed

Career Focus: Regulatory

This role is part of a curated selection of life science opportunities featured on Xtalks. Employers may request edits or removal here.

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