Sean Stowe

Experience

• 

  North Carolina State University

  Aug 2007 - Sept 2013

  Work on: 1) the structures and binding interactions of B. subtilis proteins, 2) a series of bioassays using C. elegans that measure developmental and reproductive toxicity, bacterial pathogenicity, and drug effectiveness, and 3) determining anti-biofilm drug mechanisms action using direct and indirect methods. Work on: 1) the structures and binding interactions of B. subtilis proteins, 2) a series of bioassays using C. elegans that measure developmental and reproductive toxicity, bacterial pathogenicity, and drug effectiveness, and 3) determining anti-biofilm drug mechanisms action using direct and indirect methods.

  • Postdoctoral Researcher

    Mar 2013 - Sept 2013

  • Graduate Student/ Research Assistant

    Aug 2007 - Mar 2013
• 

  University of Maryland School of Medicine

  Oct 2013 - Feb 2016

  Postdoctoral Researcher

  Serve as a project manager and primary researcher on several drug discovery and development projects, focusing on targeting proteins involved in post-transcriptional regulation and survival in melanoma, lymphoma (DLBCL) and breast cancer.

• 

  Catalent Pharma Solutions

  Mar 2016 - Mar 2017

  Aid our customers in the development, qualification, and release analysis of their large molecule/biologic products and methods using a variety of techniques ranging from analytical HPLC to structural analysis. Aid our customers in the development, qualification, and release analysis of their large molecule/biologic products and methods using a variety of techniques ranging from analytical HPLC to structural analysis.

  • Scientist

    Jan 2017 - Mar 2017

  • Sr. Associate Scientist

    Mar 2016 - Jan 2017
• 

  Grifols

  Apr 2017 - Aug 2018

  Research Scientist

  As part of the BioAnalytics R&D team, I aid in the development, optimization, and qualification of methods for the analysis of extractable and leachable substances, excipients, and final or intermediate products. In addition to development, we are involved in purity and particle analysis for stability studies and assist in lot or process investigations.

• 

  FUJIFILM Diosynth Biotechnologies

  Sept 2018 - Jan 2024

  • Responsible for global process design and implementation for Process Development Electronic Laboratory Notebook and Inventory management platform and associated systems across all sites.• Manage platform support and design teams at both site and global levels.• Monitor the usage of system and adherence to platform guidelines.• Tracking and communication of business metrics and data associated with the platform.• Ownership and maintenance of platform and associated documentation.• Ownership and management of the development, delivery, and maintenance of training across sites.• Partner and liaison with QA and IT teams for system integration, support, and continuous improvement. Show less FUJIFILM Diosynth Biotechnologies USA, Inc., Morrisville, NC September, 2018 – PresentSenior Scientist in Analytical Development• Global Technical Lead for implementation and integration of ELN system across four company sites (domestic and international).• Analytical Technical Lead and Liaison for select client programs in support of phase-specific development and cGMP manufacturing.• Manager with one direct report within program-centered team.• Author/ Reviewer/ Approver for non-GMP and cGMP Technical Methods, Standard Operating Procedures, Work Instructions, Certificates, and Reports (Workbench and Master Control).• Data Reviewer for non-GMP and GMP analytical data packets.• Project Manager/Study Sponsor for external testing and development studies with contract research organizations.• Training module development for laboratory instrumentation and GMP methods/techniques. Show less FUJIFILM Diosynth Biotechnologies USA, Inc., Morrisville, NC September, 2018 – PresentSenior Scientist in Analytical Development• Analytical Technical Lead and Liaison for select client programs in support of phase-specific development and cGMP manufacturing.• Manager with one direct report within program-centered team.• Author/ Reviewer/ Approver for non-GMP and cGMP Technical Methods, Standard Operating Procedures, Work Instructions, Certificates, and Reports (Workbench and Master Control).• Data Reviewer for non-GMP and GMP analytical data packets.• Project Manager/Study Sponsor for external testing and development studies with contract research organizations.• Training module development for laboratory instrumentation and GMP methods/techniques. Show less

  • Global Business Process Owner, PD ELN System

    Oct 2022 - Jan 2024

  • Associate Principal Scientist

    Apr 2020 - Sept 2022

  • Senior Scientist

    Sept 2018 - Apr 2020
• 

  IDBS

  Jan 2024 - now

  Senior Solutions Consultant