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Regulatory Consultant (Cmc Module 3)

Syneos Health
6-12 years
Not Disclosed
Gurugram, India
10 May 22, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company

Syneos Health

Job Title

Regulatory Consultant (CMC Module 3)
(Regulatory Affairs Consultant / Senior Regulatory Consultant – CMC)

Location

  • Gurugram

  • Hybrid (Remote + Office)

Job ID

  • 25106904

Experience Level

  • 6–12 years (Regulatory Affairs / CMC)


Company Overview

Syneos Health is a global life sciences services organization supporting drug development and commercialization across clinical development, regulatory affairs, and post-approval lifecycle management. The company collaborates with pharmaceutical innovators to accelerate global healthcare delivery.


Role Summary

The Regulatory Consultant (CMC Module 3) is responsible for authoring, reviewing, and managing Chemistry, Manufacturing, and Controls (CMC) documentation for global regulatory submissions. The role focuses on post-approval lifecycle management, regulatory variations, and ensuring compliance with global regulatory requirements, especially EU and ROW markets.


Key Responsibilities

1. CMC Regulatory Documentation (Module 3)

Authoring & Review

  • Author and review Module 3 (CMC) documentation

  • Support post-approval submissions

  • Ensure accuracy and compliance of CMC content

Technical Areas

  • API (Active Pharmaceutical Ingredient) documentation

  • Drug Product (DP) documentation

  • Manufacturing and quality-related data compilation


2. Regulatory Submissions & Variations

Variation Management

Prepare and support global variation submissions, including:

  • EU variations:

    • Type IA

    • Type IB

    • Type II

  • US submissions:

    • CBE (Changes Being Effected)

    • PAS (Prior Approval Supplement)

  • ROW (Rest of World) regulatory variations

Site Transfers

  • Manage manufacturing site transfer submissions

  • Support regulatory strategy and documentation compilation


3. Cross-Functional Collaboration

Work closely with:

  • Manufacturing teams

  • Quality Assurance (QA)

  • Quality Control (QC)

  • Supply Chain teams

Responsibilities include:

  • Data collection and verification

  • Alignment on regulatory requirements

  • Ensuring submission readiness


4. Regulatory Operations & Compliance

Submission Management

  • Track and manage regulatory activities

  • Ensure timely submissions and compliance with deadlines

Authority Interactions

  • Respond to regulatory authority queries and deficiencies

  • Ensure timely and accurate responses


5. Stakeholder Management

  • Participate in client and cross-functional meetings

  • Act as regulatory representative in discussions

  • Provide technical guidance to team members


6. Lifecycle Management

  • Support post-approval regulatory lifecycle activities

  • Manage ongoing updates to CMC documentation

  • Ensure compliance with evolving regulatory requirements


Required Skills & Expertise

CMC Regulatory Expertise

  • Strong experience in CMC Module 3 authoring and review

  • Knowledge of:

    • Drug substance and drug product lifecycle

    • Post-approval regulatory variations

    • Global CMC requirements

Regulatory Knowledge

  • Strong understanding of:

    • EU regulatory framework (mandatory

    • ROW regulatory requirements

  • Knowledge of US regulatory submission types

Technical Skills

  • Experience with eCTD submission formats

  • Familiarity with regulatory tools and documentation systems

Analytical & Operational Skills

  • Ability to manage multiple regulatory priorities

  • Strong attention to detail

  • Ability to work independently

Communication & Collaboration

  • Strong stakeholder management skills

  • Effective written and verbal communication

  • Ability to work with global, cross-functional teams


Required Qualifications

  • M.Pharm / M.Sc. or equivalent Life Sciences degree


Work Environment

  • Hybrid working model (Gurugram office + remote flexibility)

  • Global regulatory operations environment

  • High collaboration with manufacturing, QA/QC, and regulatory teams

  • Deadline-driven submission-focused workload


Career Growth Opportunities

Syneos Health offers:

  • Exposure to global regulatory submissions

  • Leadership opportunities in CMC strategy

  • Cross-functional pharmaceutical industry experience

  • Continuous professional development in regulatory affairs


Industry Impact

Over the past 5 years, Syneos Health has supported:

  • 94% of FDA-approved novel drugs

  • 95% of EMA-authorized products

  • 200+ studies across:

    • 73,000 sites

    • 675,000+ trial patients