Francis Leung Email & Phone Number | Motivated scientist with professional experience in pharmaceutical and biotechnological testing samples and raw materials product release in GMP environment. Knowledgeable in LC/MS, HPLC, Amino Acid Analysis, N-terminal sequencing, and SDS PAGE techniques. Detail-oriented and possess problem solving skills. Demonstrated working independently as well as team-player. Ability to multi-task, with excellent organizational skills and prioritization. Received commendations on consistent outstanding performance as individual and supervisory level from the United States Navy. Specialties: Perform and review release tests, stability tests, solubility test, impurity test, identification, qualification, and verification on protein drug substance, drug product, new materials, and developing materials under GMP/GSP/GLP environment.

Francis Leung

Motivated scientist with professional experience in pharmaceutical and biotechnological testing samp...
San Diego, California, United States

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Francis Leung’s Location San Diego, California, United States

Francis Leung’s Current Industry Catalent Pharma Solutions

Francis Leung’s Prior Industry Ludwig Institute For Cancer Research | United States Navy

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Associate Scientist

2008-04-01 00:00:00 - Present

Lab Assistant (Volunteer)

2009-02-01 00:00:00 - 2010-01-01 00:00:00

Petty Officer Second Class, Supervisor

1999-07-01 00:00:00 - 2004-03-01 00:00:00

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Francis Leung is a Motivated scientist with professional experience in pharmaceutical and biotechnological testing samples and raw materials product release in GMP environment. Knowledgeable in LC/MS, HPLC, Amino Acid Analysis, N-terminal sequencing, and SDS PAGE techniques. Detail-oriented and possess problem solving skills. Demonstrated working independently as well as team-player. Ability to multi-task, with excellent organizational skills and prioritization. Received commendations on consistent outstanding performance as individual and supervisory level from the United States Navy. Specialties: Perform and review release tests, stability tests, solubility test, impurity test, identification, qualification, and verification on protein drug substance, drug product, new materials, and developing materials under GMP/GSP/GLP environment.