Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Dgm / Head – Biologicals Regulatory Cmc

Sun Pharma
Sun Pharma
10-15 years
preferred by company
Gurgaon, Mumbai, Vadodara, India
1 May 14, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding

DGM / Head – Biologicals Regulatory CMC

Location: Gurgaon, Haryana, India (Preferred) / Vadodara, Gujarat, India / Mumbai, Maharashtra, India
Employment Type: Full-Time
Department: Global Regulatory Affairs / Innovative Medicines / Biologics Regulatory CMC
Experience Required: 15–20 Years
Education Required: M.Pharm / M.Tech / MS / PhD (Pharmaceutics / Biotechnology / Related Sciences)


Job Overview

A senior executive leadership opportunity is available for an experienced DGM / Head – Biologicals Regulatory CMC within the global pharmaceutical and biotechnology regulatory affairs domain. This role is ideal for highly experienced professionals with expertise in biologics regulatory strategy, CMC regulatory leadership, BLA/MAA submissions, biosimilar approvals, global market expansion, biologics lifecycle management, and cross-functional pharmaceutical leadership.

The selected candidate will lead global regulatory Chemistry, Manufacturing, and Controls (CMC) strategy for innovative biologics, established biologics, and biosimilar products across highly regulated international markets.

This is a strategic enterprise leadership role suited for professionals seeking advancement in global biologics regulatory leadership, CMC governance, international product approvals, innovative medicines strategy, and executive pharmaceutical regulatory management.


Key Responsibilities

Global Biologics Regulatory CMC Leadership

  • Lead the global biologics regulatory CMC team for established and innovative biological products
  • Define and execute global regulatory strategy for biologics development and commercialization
  • Drive regulatory planning for international markets including:
    • United States
    • European Union
    • Canada
    • Australia
    • Brazil
    • Rest of World (ROW)
  • Ensure successful regulatory approvals and lifecycle continuity for biologics portfolios

CMC Regulatory Strategy Development

  • Develop data-driven CMC regulatory strategies for biologics products across multiple development stages
  • Drive regulatory pathway planning for:
    • IND submissions
    • IMPD submissions
    • BLA filings
    • MAA submissions
    • NDA-related biologics programs
    • Lifecycle management programs
  • Assess regulatory risks and develop mitigation strategies for complex biologics programs

Global Submission Leadership
Lead and oversee preparation, review, and execution of:

  • IND applications
  • IMPD submissions
  • BLA filings
  • MAA submissions
  • NDA regulatory documentation (where applicable)
  • Health authority response packages
  • Lifecycle maintenance submissions
  • Variation filings
  • Global regulatory documentation

Ensure submission quality, compliance, and zero-defect execution standards.

Cross-Functional Development Leadership
Collaborate closely with:

  • Research & Development
  • CMC development teams
  • Manufacturing
  • Analytical development
  • Quality Assurance
  • Clinical development
  • Commercial teams
  • Supply chain
  • Project management
  • Global manufacturing sites

Drive integrated regulatory strategy aligned with business and development objectives.

Health Authority Engagement

  • Represent regulatory affairs in:
    • Health authority meetings
    • Scientific advice discussions
    • Regulatory correspondence interactions
    • Strategic regulatory negotiations
  • Guide preparation of briefing books, meeting packages, and scientific justification materials
  • Support agency interactions for developed global markets

Lifecycle Management & Strategic Portfolio Support

  • Lead lifecycle management for biologics portfolios
  • Support:
    • Product in-licensing due diligence
    • Regulatory portfolio assessments
    • Product divestment strategies
    • Product withdrawal planning
    • Market continuity activities

Biologics Technical Dossier Leadership

  • Evaluate technical and scientific data required for biologics regulatory dossiers
  • Oversee creation of zero-defect regulatory submissions
  • Review scientific justifications, technical documentation, and regulatory response strategies
  • Ensure alignment between manufacturing, testing, release, and regulatory expectations

Innovation & New Technology Support

  • Support internal innovation programs and emerging technology development
  • Enable adoption of modern regulatory strategies for innovative medicines
  • Strengthen regulatory competitiveness across global biologics programs

Team Leadership & Capability Building

  • Lead, mentor, and develop global regulatory CMC teams
  • Manage team performance, deliverables, and capability development
  • Drive high-performance execution and strong leadership culture
  • Support succession planning and technical excellence initiatives

Required Qualifications

Educational Qualifications
Candidates must hold one of the following:

  • M.Pharm
  • M.Tech
  • MS
  • PhD

Preferred specialization:

  • Pharmaceutics
  • Biotechnology
  • Pharmaceutical Sciences
  • Life Sciences
  • Related scientific disciplines