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Job title: R&D GRA CMC Lead

• Location: Hyderabad

About the job

Our Team:

​​​​The Global Regulatory Affairs (GRA) CMC & Device Organization serves as a critical strategic partner within Sanofi's regulatory framework, providing expert guidance on Chemistry, Manufacturing, and Controls (CMC) and medical device regulatory requirements across the product lifecycle. Our department bridges the gap between technical development, manufacturing operations, and global regulatory authorities to ensure compliance while optimizing product approval pathways. The team develops and implements global regulatory strategies for pharmaceutical products, biologics, vaccines, and combination products, working closely with cross-functional partners to navigate complex regulatory landscapes. With a commitment to Sanofi's "Take the Lead" values, particularly in "Leading Together" and "Being Bold," our mission is to secure timely approvals while maintaining the highest standards of quality and compliance, ultimately supporting Sanofi's goal of bringing innovative healthcare solutions to patients worldwide.​ 

Main responsibilities:

Develop and implement global regulatory CMC strategies, create strategies for development and marketed products, focus on chemical entities, biological entities, and/or vaccine products, execute and adapt strategies as needed 

Serve as the primary point of contact for regulatory authorities, Act as direct liaison with agencies like US FDA and EMA, Develop positive relationships with regulators ,Support strategic negotiations with worldwide Regulatory Health Authorities 

Manage CMC documentation and submissions, Write, prepare, review, and approve regulatory CMC dossiers, ensure dossiers meet quality standards, comply with regulatory requirements, Maintain documentation accuracy and completeness 

Lead cross-functional collaboration, work closely with R&D Functions, Collaborate with Manufacturing & Supply Functions, Coordinate with GRA Regulatory Operations, ensure effective implementation of regulatory strategies, Facilitate resolution of CMC issues 

Identify and manage regulatory risks, assess regulatory CMC opportunities and risks, develop risk mitigation strategies, communicate implications to project teams, Articulate risk/benefit components to stakeholders 

Contribute to regulatory science and policy activities, monitor local and international Health Authority regulations and guidelines, participate in the review process for new regulations, anticipate potential regulatory paradigm shifts, Track and communicate current Health Authority thinking and trends 

About you

• Experience in the pharmaceutical industry with strong expertise in CMC Regulatory Affairs.

• Strong understanding of drug development, manufacturing, and testing processes, Good understanding of Artificial Intelligence applications in regulatory affairs

• Experience with combination (drug/device) productsAdvanced proficiency in regulatory documentation preparation

• Comprehensive knowledge of global regulatory requirements, Experience with complex regulatory submissions

• Demonstrated leadership in matrix environment,Proven ability to influence cross-functional stakeholders

• Experience managing multiple high-priority products simultaneouslyAdvanced communication skills with ability to persuade and negotiate

• Strong mentoring capabilitiesStrategic thinking and decision-making abilities

• Advanced communication skills with ability to persuade and negotiate Stakeholder management Adaptability & flexibility Critical thinking & Problem-solving Teamwork & collaboration Time management Emotional intelligence (EQ)Compliance & quality mindset Proactive ownership Presentation skills

• Technical skills: Strategic ThinkingResults-Oriented People LeadershipInfluencing Others Regulatory Strategies Product Registrations Risk Management Digital AdoptionStakeholder Management Advanced proficiency in MS Office Suite & Electronic document management systems (Veeva vault, Plai)

Pursue Progress, discover Extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN videoand check out our Diversity Equity and Inclusion actions at sanofi.com!

Pursue Progress. Discover Extraordinary.

Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.

Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com