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Associate Manager - Cmc Regulatory

Elanco
5+ years
₹18 – ₹30 LPA
Bangalore, India
15 July 20, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

Associate Manager – CMC Regulatory | Elanco

Job Details

  • Job Title: Associate Manager – CMC Regulatory

  • Company: Elanco

  • Job ID (Req ID): R0025826

  • Location: Bangalore, Karnataka, India

  • Job Type: Full-time

  • Department: Regulatory Affairs – CMC

  • Experience Required: 5+ years

  • Travel Requirement: 0%

  • Estimated Salary Package (Market Standard): ₹18 – ₹30 LPA (depending on CMC regulatory expertise, global submission experience, and industry background)


About the Company

Elanco is a global leader in animal health, focused on developing innovative products and solutions to prevent and treat diseases in farm animals and pets. The company works with global R&D, manufacturing, quality, and regulatory teams to deliver safe and effective animal health products worldwide.


Job Purpose

The Associate Manager – CMC Regulatory will be responsible for developing and executing global Chemistry, Manufacturing & Controls (CMC) regulatory strategies, managing post-approval lifecycle activities, supporting regulatory submissions, and ensuring compliance with global regulatory requirements for animal health products.


Key Responsibilities

CMC Regulatory Strategy & Lifecycle Management

  • Develop and execute CMC regulatory strategies for marketed products.

  • Manage end-to-end Life Cycle Management (LCM) activities for:

    • Small molecules.

    • Large molecules.

    • Complex dosage forms.

    • Sterile preparations.

    • Biotechnology-derived products.

    • Specialized dosage forms.

  • Balance regulatory compliance with business objectives through innovative regulatory approaches.

  • Support supplements, variations, renewals, and annual reporting requirements.


Regulatory Submission Management

  • Lead preparation and submission of CMC regulatory dossiers across multiple global regions.

  • Ensure submission documents meet regulatory quality standards.

  • Author high-quality CMC regulatory documentation.

  • Communicate submission requirements, timelines, and documentation needs to cross-functional teams.

  • Track submission activities according to regulatory procedures.


Cross-Functional Collaboration

  • Collaborate with:

    • Manufacturing teams.

    • Quality Assurance.

    • Research & Development.

    • Global regulatory teams.

    • External regulatory partners.

  • Communicate regulatory strategies, critical issues, and project updates effectively.

  • Support global regulatory business objectives.


Regulatory Compliance & Knowledge Management

  • Maintain current knowledge of:

    • FDA/CVM guidelines.

    • EMA requirements.

    • VICH guidelines.

    • Global regulatory trends.

  • Monitor new technical and regulatory developments.

  • Ensure compliance with:

    • cGMP requirements.

    • Regional regulatory standards.

  • Provide training and mentorship to CMC regulatory team members.


Required Qualifications

  • Degree in:

    • M.Sc.

    • B.Pharm / M.Pharm

    • Postgraduate degree in Veterinary Sciences

    • Other relevant scientific disciplines

  • 5+ years of experience in Global Regulatory Affairs, preferably in:

    • Post-approval CMC lifecycle management.

    • Pharmaceutical or animal health regulatory environments.


Preferred Qualifications

  • Strong knowledge of:

    • FDA/CVM guidelines.

    • EMA guidelines.

    • VICH guidelines.

  • Experience with CMC registrations in:

    • USA.

    • Europe.

    • Rest of the World (ROW).

  • Experience managing multiple pharmaceutical dosage forms.

  • Experience with Regulatory Information Management (RIM) tools and systems.


Preferred Skills

  • CMC Regulatory Affairs.

  • Regulatory strategy development.

  • Post-approval lifecycle management.

  • Global regulatory submissions.

  • Pharmaceutical development knowledge.

  • FDA/CVM and EMA regulatory compliance.

  • VICH guideline understanding.

  • cGMP requirements.

  • Regulatory documentation writing.

  • Dossier preparation and review.

  • Stakeholder management.

  • Project management.

  • Quality-focused approach.

  • Strong written and verbal communication.


One-Line Experience

Candidates with 5+ years of experience in global CMC Regulatory Affairs, post-approval lifecycle management, and regulatory submissions for pharmaceutical or animal health products are preferred.


Salary Package

  • Estimated CTC: ₹18 – ₹30 LPA

  • Mid-Level CMC Regulatory Professionals: ₹18 – ₹25 LPA

  • Experienced Global Regulatory Specialists: ₹25 – ₹35 LPA+ depending on expertise.

(Actual compensation may vary based on Elanco’s internal salary structure, global regulatory experience, and CMC specialization.)


Why Join Elanco?

  • Opportunity to work with a global animal health leader.

  • Exposure to international regulatory submissions and lifecycle management.

  • Work with global regulatory, manufacturing, and quality teams.

  • Leadership role in CMC regulatory strategy and compliance.

  • Strong career growth opportunities in global regulatory affairs.