Experience

Invivyd

• United States
• Biotechnology Research
• 1 - 100 Employee

• Senior Director, Head of Drug Product Manufacturing and Clinical Supply Chain

  • Nov 2020 - Present



Syndax Pharmaceuticals

• United States
• Biotechnology Research
• 1 - 100 Employee

• Director, Pharmaceutical Development and Manufacturing

  • Jul 2019 - Oct 2020

• Associate Director, Pharmaceutical Development and Manufacturing

  • Apr 2017 - Jul 2019



Receptos, a wholly-owned subsidiary of Celgene

• United States
• Biotechnology Research
• 1 - 100 Employee

• Associate Director, Biopharmaceutical Manufacturing

  • Oct 2014 - Mar 2017



Shire

• Japan
• Biotechnology Research
• 700 & Above Employee

• Associate Director, Manufacturing

  • 2010 - 2014

  Manufacturing Leader for project SHORE (Shire's Operation for Regenerative Expansion), a $175M Technical Operations new facility expansion project in the Sorrento Valley area of San Diego, CA. Prior leadership roles as Senior Manager/Manager, Manufacturing involved managing internal cGMP Manufacturing operations. Directly responsibility for Cell Culture, Production Support, Media Prep, and Packaging. Manufacturing Leader for project SHORE (Shire's Operation for Regenerative Expansion), a $175M Technical Operations new facility expansion project in the Sorrento Valley area of San Diego, CA. Prior leadership roles as Senior Manager/Manager, Manufacturing involved managing internal cGMP Manufacturing operations. Directly responsibility for Cell Culture, Production Support, Media Prep, and Packaging.



Biotech Industry

• Greater San Diego Area

• Independent Consultant

  • 2006 - 2009

  Provide independent consulting services to biotechnology companies including development and review of cGMP documentation and validation protocols, process validation strategy assessment, establishment of cleanroom production policies and procedures, and developing a company quality manual. Provide independent consulting services to biotechnology companies including development and review of cGMP documentation and validation protocols, process validation strategy assessment, establishment of cleanroom production policies and procedures, and developing a company quality manual.



Favrille, Inc.

• Greater San Diego Area

• Senior Manager, Fill Finish and Production Support

  • 2002 - 2006



IDEC Pharmaceuticals

• Greater San Diego Area

• Project Manager, Manufacturing Operations

  • 2002 - 2002



Advanced Tissue Sciences

• Greater San Diego Area

• Senior Manager, Manufacturing

  • 1995 - 2002



Molecular Biosystems

• Greater San Diego Area

• Supervisor, Manufacturing

  • 1993 - 1995



Biosurface Technology / Genzyme Tissue Repair

• Greater Boston Area

• Supervisor, Production

  • 1990 - 1993