Shao Siong Chua
About
Shao Siong Chua is from Singapore. Shao Siong works in the following industries: "Biotechnology Research". Shao Siong is currently GM, Manufacturing Operations, Singapore at RVAC Medicines, located in Singapore. In Shao Siong's previous role as a Head Manufacturing Unit (BioProduction Ops) at Novartis, Shao Siong worked in Singapore until Dec 2021. Prior to joining Novartis, Shao Siong was a Site Head (ad-interim) at Novartis and held the position of Site Head (ad-interim) at Singapore. Prior to that, Shao Siong was a Production Lead (Site Expansion Project) at Novartis, based in Singapore from Mar 2016 to Mar 2017. Shao Siong started working as Head of Manufacturing at Baxalta in Singapore in Jul 2015. From Jun 2010 to Jun 2015, Shao Siong was Head of Manufacturing at Baxter International Inc., based in Singapore. Prior to that, Shao Siong was a Value Stream Mfg Lead at GSK, based in Singapore from Jan 2009 to May 2010. Shao Siong started working as R&D Operations Lead at GSK in singapore in Jan 2006.
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Shao Siong Chua's current jobs
Shao Siong Chua's past jobs
Responsible for manufacturing operations associated with clinical and commercial GMP production of bulk biologic drug substances, from Cell Culture to Purification and Manufacturing Support services.
Responsible for overall Singapore biologics manufacturing operations. Represented Singapore Site in the Novartis Large Molecules platform comprises of other Sites and global functions. Member of the Novartis Country Leadership Team.
Responsible for the user input of the site expansion project and the subsequent manufacturing operations associated with commercial GMP production of biologic bulk drugs, from Cell Culture to Purification.
Responsible for manufacturing operations associated with commercial GMP production of bulk recombinant protein, from Cell Culture to Purification and Manufacturing Support.
Responsible for manufacturing operations associated with commercial GMP production of bulk recombinant protein, from Cell Culture to Purification and Manufacturing Support.
Responsible for manufacturing operations associated with commercial GMP production of active pharmaceutical ingredients.
Responsible for manufacturing operations associated with development of new chemical entities and the manufacturing of clinical trials pharmaceutical ingredients.
Experienced in Black Belt application in pharmaceutical industries.
Responsible for commissioning of new facility and processes. In addition to being a lead engineer for production of active pharmaceutical ingredients.
Responsible for unit operations and technical support for the manufacturing of Adipure.