Senior Manager - CMC Regulatory Affairs Biopharm Development Projects
1925 GlaxoSmithKline LLCJob Description
Senior Manager - CMC Regulatory Affairs Biopharm Development Projects
At 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 R&D 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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This position is responsible for leading CMC regulatory activities for investigational, late development and/or early commercial GSK products.
Key Responsibilities:
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