Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Sr Publisher I/ Ii

Novo Nordisk
6-7+ years
₹18–30 LPA
Bangalore, India
15 July 16, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Basic Statistics Interpretation, Clinical Research Knowledge, Evidence Synthesis, Literature Review, Medical Writing, MS Word, Narrative Writing, Scientific Writing

Job Title: Sr Publisher I / II

Company: Novo Nordisk Global Business Services (GBS)

Location: Bangalore, Karnataka, India

Employment Type: Full-time

Department: Regulatory Publishing – Clinical Development, Research & Development

Experience Required: 6–7+ years of experience in Pharmaceutical Regulatory Publishing, eCTD submissions, dossier compilation, and global regulatory submissions (EU/FDA experience preferred).

Education: Bachelor's or Master's degree in Pharmacy, Life Sciences, Science, or a related field.

Salary Package: ₹18–30 LPA (Estimated as per current market standards for Senior Regulatory Publishing roles in multinational pharmaceutical companies; final compensation depends on experience, technical expertise, and interview performance.)

Key Responsibilities:

  • Lead end-to-end regulatory publishing activities for global and regional submissions.

  • Plan, compile, publish, validate, and dispatch regulatory submissions within timelines.

  • Manage submissions including:

    • MAA (Marketing Authorisation Applications)

    • NDA (New Drug Applications)

    • Post-Approval Changes

    • Lifecycle Management submissions

  • Ensure eCTD compliance according to global Health Authority requirements.

  • Compile and publish clinical, non-clinical, and safety documentation.

  • Perform electronic Quality Control (eQC) of regulatory submission documents.

  • Act as Lead Publisher and primary contact for assigned projects.

  • Coordinate with Regulatory Affairs, Clinical, Safety, and Non-Clinical teams.

  • Ensure compliance with templates, style guides, publishing standards, and timelines.

  • Support SOP development, process improvements, and publishing optimization.

  • Drive inspection readiness and identify compliance risks.

  • Mentor and train publishing team members through knowledge sharing and onboarding.

Required Skills:

  • Regulatory Publishing

  • eCTD Publishing

  • NeeS Submissions

  • Regulatory Submission Management

  • Dossier Compilation

  • Electronic Document Management Systems (EDMS)

  • Regulatory Information Management Systems

  • EMA & FDA Submission Requirements

  • ICH Guidelines

  • Electronic Quality Control (eQC)

  • Document Formatting & Publishing Standards

  • GxP Compliance

  • Stakeholder Management

  • Process Improvement

  • Automation & Digital Tools

  • Attention to Detail

Preferred Skills:

  • Experience handling EU regulatory submissions.

  • Strong knowledge of global regulatory publishing standards.

  • Experience with regulatory publishing platforms and document management systems.

  • Exposure to AI, automation, and technology-driven publishing improvements.

  • Experience mentoring junior publishers.

  • Ability to independently manage complex regulatory projects.

Work Mode: Office-Based / Hybrid (Bangalore)

Benefits:

  • Competitive salary and career growth opportunities.

  • Exposure to global regulatory submissions and innovative therapies.

  • Opportunity to work with international regulatory and clinical teams.

  • Continuous learning and professional development.

  • Collaborative global R&D environment.

  • Opportunity to contribute to faster delivery of life-changing medicines.