Senior CMC Regulatory Product Lead - Vaccine Submissions
GlaxoSmithKline Pte Ltd
SingaporePosted 27 days agoDiscoveredMatch locked
HybridFull-time8+ years expAdmin Jobs
About the role
GlaxoSmithKline Pte Ltd is seeking a seasoned CMC Regulatory Affairs leader to coordinate complex submissions and post-approval changes across vaccines. You will collaborate with quality, supply chain, and external partners to deliver submission-ready documentation on time. The role requires 8 years in regulatory affairs/CMC, CTD Module 3 experience, and strong project management. Hybrid work with
Not included in the source posting: about the role, what you'll do, qualifications, benefits.
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