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Regulatory Consultant (Cmc Module 3)

Syneos Health
6-12 years
Not Disclosed
Remote, India, India
9 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

Regulatory Consultant (CMC Module 3)

Company: Syneos Health
Location: IND – Remote
Job ID: 25106904
Updated On: May 18, 2026
Experience Level: 6–12 years
Qualification: M.Pharm / M.Sc. or equivalent Life Sciences degree


Company Overview

Syneos Health is a global life sciences services organization that supports drug development and commercialization. It works across clinical development, regulatory affairs, and post-approval lifecycle management to help pharmaceutical companies bring therapies to market efficiently.


Role Summary

The Regulatory Consultant (CMC Module 3) is responsible for:

  • Authoring and reviewing CMC (Chemistry, Manufacturing & Controls) Module 3 documentation

  • Supporting post-approval regulatory lifecycle activities

  • Managing global regulatory submissions and variations

  • Ensuring compliance with EU, US, and ROW regulatory requirements


Key Responsibilities

1. CMC Documentation & Authoring

  • Author and review Module 3 (CMC) documentation

  • Support post-approval submissions and lifecycle management activities

  • Ensure accuracy, completeness, and regulatory compliance of CMC content


2. Regulatory Submissions & Variations

  • Prepare variation applications:

    • EU: Type IA, IB, II

    • US: CBE, PAS

    • ROW regulatory variations

  • Manage regulatory submissions related to site transfers

  • Support compilation of submission dossiers


3. Cross-Functional Collaboration

  • Work with Manufacturing, QA, QC, and Supply Chain teams

  • Collect, verify, and validate technical and quality data

  • Participate in cross-functional and client meetings


4. Regulatory Strategy & Compliance

  • Ensure compliance with global regulatory requirements

  • Track submission timelines and regulatory deliverables

  • Respond to regulatory authority queries and deficiency letters


5. Project & Stakeholder Management

  • Manage multiple regulatory activities simultaneously

  • Ensure adherence to scope, timelines, and budget

  • Communicate progress to internal and external stakeholders

  • Provide guidance and troubleshooting support to team members


Required Skills & Expertise

  • Strong experience in CMC authoring (Module 3)

  • Expertise in post-approval lifecycle management

  • Knowledge of:

    • EU regulatory requirements (mandatory)

    • ROW markets

    • API and Drug Product (DP) variations

  • Familiarity with eCTD submissions and regulatory tools

  • Strong communication and stakeholder management skills

  • Ability to work independently and handle multiple priorities


Preferred Competencies

  • Regulatory strategy experience for global markets

  • Experience handling complex CMC variations

  • Strong problem-solving and coordination skills

  • Detail-oriented documentation and compliance mindset


Work Environment

  • Fully remote (India-based)

  • Global cross-functional collaboration

  • High-volume regulatory submission environment

  • Client-facing regulatory consulting role


Role Impact

  • Ensures timely approval of post-market changes

  • Supports global availability of pharmaceutical products

  • Plays a key role in maintaining regulatory compliance across markets

  • Direct impact on product lifecycle continuity and supply chain stability