Megan Sun Email & Phone Number | • M.S. in chemistry and 11 years of pharmaceutical industry experience in drug discovery and development focusing on small molecules. • Strong in analytical and organic chemistry. Hands-on skills include: HPLC; LC/MS; GC; GC/MS; Ion chromatography (IC); TGA, DSC and XRPD for solid state analysis; particle size; dissolution testing; Nuclear Magnetic Resonance Spectroscopy (NMR), Preparative HPLC, etc. • Strong in designing and writing study protocols in compliance with applicable FDA guidances and ICH guidelines. Experienced in managing stability programs, data trending and developing analytical method to support process chemistry and formulation development. • Strong in structure elucidation, impurity identification and laboratory documentation to support cGMP operations and CMC regulatory filing. • Hold Regulatory Affairs Certificate from UCSC extension and possess extensive regulatory knowledge applicable in drug development process. Experienced in CMC section (Module 3) regulatory filings. • Motivated self-starter with experience integrating my knowledge on synthetic and analytical chemistry into pharmaceutical development.

Megan Sun

• M.S. in chemistry and 11 years of pharmaceutical industry experience in drug discovery and develop...
18785 Tilson Avenue, Cupertino, United States

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Megan Sun’s Email sun.megan@gene.com

Megan Sun’s Phone Numbers +1 877-436-****

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Megan Sun’s Location 18785 Tilson Avenue, Cupertino, United States

Megan Sun’s Current Industry Genentech Roche Genentech

Megan Sun’s Prior Industry Proteolix | Millennium Pharmaceuticals | Exelixis

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Megan Sun is a • M.S. in chemistry and 11 years of pharmaceutical industry experience in drug discovery and development focusing on small molecules. • Strong in analytical and organic chemistry. Hands-on skills include: HPLC; LC/MS; GC; GC/MS; Ion chromatography (IC); TGA, DSC and XRPD for solid state analysis; particle size; dissolution testing; Nuclear Magnetic Resonance Spectroscopy (NMR), Preparative HPLC, etc. • Strong in designing and writing study protocols in compliance with applicable FDA guidances and ICH guidelines. Experienced in managing stability programs, data trending and developing analytical method to support process chemistry and formulation development. • Strong in structure elucidation, impurity identification and laboratory documentation to support cGMP operations and CMC regulatory filing. • Hold Regulatory Affairs Certificate from UCSC extension and possess extensive regulatory knowledge applicable in drug development process. Experienced in CMC section (Module 3) regulatory filings. • Motivated self-starter with experience integrating my knowledge on synthetic and analytical chemistry into pharmaceutical development.