Regulatory Associate Manager - Product Variations, CD CMC

• Business IntroductionAt GSK, we have bold ambitions for patients, aiming to positively impact the health of 2
• 5 billion people by the end of the decade
• Our RD focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people s lives
• GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients needs and have the highest probability of success
• We re uniting science, technology, and talent to get ahead of disease together

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Our approach to RDPosition SummaryYou will lead regulatory activities for product variations within Clinical Development CMC

• You will work closely with colleagues across supply chain, quality, clinical operations and external manufacturing partners
• We value clear thinking, practical problem solving and attention to quality
• This role offers exposure to global submissions and complex projects and a chance to grow as you help bring safe, compliant products closer to patients
• Join us to use your skills for meaningful impact while developing your regulatory career
• ResponsibilitiesThis role will provide YOU the opportunity to lead key activities to progress YOUR career
• These responsibilities include some of the following:- Manage end-to-end regulatory activities for product variations, from planning through submission and approval
• - Prepare, review and approve CMC sections for global regulatory dossiers and variation submissions
• - Assess data and documentation for completeness, regulatory fit and quality; identify gaps and raise clear escalations
• - Coordinate with supply chain, quality, clinical teams and external manufacturers to gather submission-ready materials
• - Identify regulatory risks and propose practical mitigation options to support timely approvals
• - Share knowledge, coach colleagues and help improve regulatory processes and tools
• Why YouThis role is on-site in India with regular collaboration across global teams
• We welcome applicants from all backgrounds and perspectives
• You will join a supportive team that values learning, career growth and making a measurable difference for patients
• If you want to deepen your expertise in regulatory CMC and play a key role in product lifecycle management, we encourage you to apply
• Basic QualificationWe are seeking professionals with the following required skills and qualifications to help us achieve our goals:- Bachelor s degree in chemistry, pharmacy, pharmaceutical sciences or a related science/technical field
• - Minimum 5 years of regulatory affairs experience focused on CMC and product variations
• - Experience preparing or managing CMC dossier components for regulatory submissions
• - Knowledge of global regulatory guidelines and expectations for CMC content
• - Strong organisational skills and experience managing multiple projects and deadlines
• - Good written and verbal communication skills in English for clear dossier writing and stakeholder engagement
• Preferred QualificationIf you have the following characteristics, it would be a plus:- 6 to 10 years experience in pharmaceutical regulatory CMC, including global submissions
• - Experience working with contract manufacturing organisations and supply chain partners
• - Prior experience as a dossier reviewer or approver
• - Ability to interpret and advise on regional regulatory requirements
• - Experience mentoring or training junior staff and building capability
• - Comfortable working in a matrix environment with cross-functional teams
• How to applyWe want to hear from you
• If this role fits your experience and ambitions, please apply now
• Include your CV and a short note about why you want to join our team