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Senior Regulatory Affairs Consultant

Parexel
10-14 years
28 LPA - 40 LPA
Bangalore, India
1 June 30, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Senior Regulatory Affairs Consultant – CMC Biologics

Company: Parexel
Location: Bengaluru, India (Remote)
Department: Regulatory Affairs – CMC Biologics
Job Type: Full-Time
Work Mode: Remote

JOB OVERVIEW

The Senior Regulatory Affairs Consultant – CMC Biologics is responsible for leading global Chemistry, Manufacturing, and Controls (CMC) regulatory activities for biological products, including vaccines, recombinant proteins, monoclonal antibodies, and plasma-derived therapies. The role involves preparing and reviewing regulatory submissions, managing product registrations and lifecycle maintenance, developing global regulatory strategies, ensuring compliance with international regulatory requirements, and mentoring regulatory teams while supporting submissions across major global markets.


KEY RESPONSIBILITIES

Global Regulatory Strategy

  • Develop regulatory strategies for biological products across global markets.

  • Support global and regional regulatory planning.

  • Ensure alignment with international regulatory requirements.

  • Provide strategic regulatory guidance throughout the product lifecycle.

  • Monitor evolving regulatory requirements and industry trends.

Regulatory Submission Management

  • Prepare, author, review, and submit CMC regulatory documents.

  • Support Marketing Authorization Applications (MAAs).

  • Prepare and manage regulatory variations and amendments.

  • Coordinate submission activities across multiple global regions.

  • Ensure timely delivery of high-quality regulatory submissions.

Product Registration & Lifecycle Management

  • Manage new product registrations for biologics.

  • Support lifecycle maintenance and post-approval changes.

  • Coordinate product renewals and regulatory variations.

  • Maintain regulatory compliance throughout the product lifecycle.

  • Track submission status and regulatory commitments.

CMC Regulatory Affairs

  • Provide CMC regulatory expertise for biological products.

  • Review manufacturing and quality documentation for submissions.

  • Ensure compliance with ICH CMC guidelines.

  • Support regulatory requirements related to manufacturing changes.

  • Maintain consistency of CMC documentation across global submissions.

Global Regulatory Compliance

  • Interpret global pharmaceutical legislation and regulatory guidance.

  • Ensure compliance with FDA, EMA, PMDA, Health Canada, Swissmedic, TGA, and ICH requirements.

  • Monitor regulatory policy changes across international markets.

  • Support responses to regulatory authority questions.

  • Ensure regulatory documentation meets global standards.

Cross-Functional Collaboration

  • Collaborate with CMC, Quality, Manufacturing, Clinical, and Regulatory teams.

  • Coordinate submission activities with global stakeholders.

  • Support project planning and regulatory timelines.

  • Communicate regulatory strategies across functional teams.

  • Provide regulatory expertise during project discussions.

Leadership & Mentoring

  • Lead and mentor regulatory affairs team members.

  • Provide technical guidance on global regulatory submissions.

  • Review team deliverables for quality and compliance.

  • Support knowledge sharing and capability development.

  • Drive continuous improvement in regulatory processes.


EDUCATIONAL QUALIFICATIONS

Required

Bachelor's Degree in:

  • Pharmacy (B.Pharm / M.Pharm)

  • Biotechnology

  • Life Sciences

  • Biochemistry

  • Microbiology

  • Biomedical Sciences

  • Chemical Engineering

  • Or another Scientific or Technical discipline

Preferred

  • Master's Degree

  • PhD

  • Or another Advanced Scientific Degree


EXPERIENCE REQUIREMENTS

Required

  • 10–14 years of experience in:

    • Regulatory Affairs

    • CMC Regulatory Affairs

    • Biologics Regulatory Submissions

Required Experience

  • Biological product registrations.

  • Product lifecycle maintenance.

  • Regulatory renewals and variations.

  • Marketing Authorization Applications (MAAs).

  • Global CMC regulatory submissions.

  • Team leadership and mentoring.