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Manager, Cmc Vaccines Mature Projects – Regulatory Affairs

GSK plc
2+ years
INR 12 LPA – 18 LPA
Remote
1 June 18, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model

Manager, CMC Vaccines Mature Projects – Regulatory Affairs

Employment Type: Full Time
Work Model: Hybrid (Remote & On-site)


Job Overview

The Manager, CMC Vaccines Mature Projects – Regulatory Affairs is responsible for leading Chemistry, Manufacturing and Controls (CMC) regulatory activities for mature vaccine products and lifecycle management programs. The role supports global regulatory submissions, manufacturing changes, product maintenance activities, and supply continuity initiatives while ensuring compliance with global regulatory requirements.

This position works closely with regulatory, quality, manufacturing, development, and supply chain teams to deliver successful regulatory outcomes and maintain uninterrupted product availability across global markets.


Key Responsibilities

CMC Regulatory Strategy & Planning

  • Lead CMC regulatory planning and execution for mature vaccine products.

  • Develop regulatory strategies supporting product lifecycle management.

  • Evaluate regulatory risks and provide mitigation plans.

  • Ensure regulatory activities align with business objectives and supply requirements.

  • Provide strategic regulatory guidance to project teams.

Regulatory Submission Management

  • Prepare, review, and quality-check CMC documentation for:

    • Regulatory Submissions

    • Variations

    • Post-Approval Changes

    • Maintenance Filings

    • Manufacturing Changes

  • Support compilation and submission of global regulatory dossiers.

  • Ensure submission packages meet regional regulatory requirements.

  • Coordinate document reviews and approvals across stakeholders.

Global Dossier Coordination

  • Manage global dossier assembly activities.

  • Coordinate cross-functional review cycles.

  • Track submission timelines and deliverables.

  • Ensure consistency and quality of CMC documentation across regions.

  • Support responses to regulatory authority questions and requests.

Cross-Functional Collaboration

  • Collaborate with:

    • Regulatory Affairs Teams

    • Manufacturing Teams

    • Quality Assurance

    • Supply Chain

    • Process Development

    • Clinical Development

  • Assess impact of manufacturing and process changes on regulatory submissions.

  • Support project teams in achieving regulatory and business objectives.

Supply Continuity Support

  • Ensure regulatory requirements supporting product supply are fulfilled.

  • Support manufacturing site changes, process improvements, and distribution activities.

  • Facilitate timely approvals to prevent supply disruptions.

  • Provide regulatory input for product release and distribution strategies.

CMC Regulatory Expertise

  • Serve as Subject Matter Expert (SME) for CMC regulatory requirements.

  • Provide guidance on:

    • Vaccine CMC Requirements

    • Biologics Regulations

    • Regulatory Dossier Formats

    • Global Submission Requirements

  • Share regulatory best practices across project teams.

Regulatory Compliance & Inspections

  • Ensure compliance with:

    • Global Regulatory Requirements

    • GMP Standards

    • CMC Submission Standards

    • Internal Policies and Procedures

  • Support regulatory inspections and audit activities.

  • Provide regulatory input during manufacturing and quality audits.

Process Improvement

  • Identify opportunities to improve regulatory operations.

  • Drive efficiency initiatives and process enhancements.

  • Contribute to development of regulatory best practices.

  • Support implementation of new regulatory tools and systems.


Qualifications

Education

  • Bachelor's Degree in:

    • Pharmacy

    • Chemistry

    • Biotechnology

    • Life Sciences

    • Related Scientific Discipline

Preferred Qualifications

  • Master's Degree

  • PhD

  • Regulatory Affairs Certification


Experience (Minimum Required)

  • Minimum 2+ years of experience in:

    • CMC Regulatory Affairs

    • Pharmaceutical Development

    • Biopharmaceutical Development

    • Regulatory Submission Activities