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Regulatory Consultant (Row Mkt Exp And Cmc – Module 3 Exp)

Syneos Health
Syneos Health
6-9 years
Not Disclosed
Gurugram, India
10 May 13, 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 (ROW Markets & CMC – Module 3 Experience)

Company: Syneos Health
Location: India – Gurugram (Hybrid)
Experience Required: 6–9 years
Job Type: Regulatory Affairs Consultant


Role Overview

The Regulatory Consultant will provide regulatory and technical support across global product development programs, with a focus on Rest of World (ROW) markets and CMC (Chemistry, Manufacturing & Controls) Module 3 documentation. The role involves managing regulatory submissions, post-approval variations, and health authority interactions while ensuring compliance with global regulatory standards.


Key Responsibilities

Regulatory Submissions & Strategy

  • Conduct regulatory research and gap analysis for global/regional requirements

  • Support preparation of IND, NDA, MAA, PMA, CTD, and other regulatory submissions

  • Prepare briefing packages for regulatory agency meetings and scientific advice interactions

  • Contribute to product development plans and regulatory strategies across lifecycle stages

Post-Approval & Lifecycle Management

  • Manage post-approval variations and maintenance activities

  • Handle API and Drug Product variations, including site transfers

  • Respond to Health Authority Questions (RTQs) and support agency communications

Project & Cross-Functional Support

  • Manage day-to-day regulatory deliverables within timelines and budgets

  • Work with clinical, technical, and cross-functional teams globally

  • Provide SME support and troubleshooting for regulatory issues

Compliance & Documentation

  • Ensure compliance with global regulatory requirements and company SOPs

  • Contribute to SOP development and process improvements

  • Support audits and internal regulatory initiatives

  • Maintain training records and complete required training programs

Business & Client Support

  • Assist in preparing regulatory service estimates for proposals

  • Support client meetings and project updates

  • Contribute to regulatory training materials and best practices sharing


Required Qualifications

  • Bachelor’s or PhD in Life Sciences, Pharmacy, or related scientific field (or equivalent experience)

  • 6–9 years of regulatory affairs experience in pharma/medical devices

  • Strong experience with:

    • ROW regulatory markets

    • CMC Module 3 documentation

    • Post-approval variations

    • Regulatory submissions (IND, NDA, MAA, CTD)

    • Health Authority interactions (RTQs)

    • API and drug product lifecycle management


Skills & Competencies

  • Strong regulatory knowledge and analytical ability

  • Excellent written and verbal communication skills

  • Ability to work independently and in cross-functional teams

  • Strong attention to detail and quality focus

  • Ability to manage multiple parallel regulatory projects

  • Proficiency in Microsoft Office tools

  • Adaptability, initiative, and problem-solving ability


Additional Expectations

  • Experience supporting global regulatory submissions

  • Ability to interact with clients and regulatory authorities

  • Contribution to continuous improvement and SOP development

  • Strong understanding of regulatory compliance frameworks