LUCY KIPYATOR
Santa Clara
Summary
Versatile research professional with extensive experience in analytical method development, validation, and troubleshooting for small molecule drug candidates. Skilled in chromatography (HPLC, UPLC, GC), spectroscopy (UV-Vis, FTIR), and titration methods (Karl Fischer). Proven ability to collaborate across cross-functional teams, ensure regulatory compliance (GLP, GMP), and deliver accurate, reliable results in fast-paced laboratory environments.
Overview
5
5
years of professional experience
Work History
Formulation Chemist
Eurofins Inc.
10.2023 - 03.2024
- Developed and validated analytical methods using HPLC, UPLC, GC, Karl Fischer titration, and UV/Vis spectroscopy for small molecule analysis.
- Performed data analysis and troubleshooting to ensure accurate and reliable results, thus, improving method efficiency.
- Prepared technical reports and presentations, effectively communicating findings to cross-functional teams.
- Maintained compliance with Good Laboratory Practices (GLP) and ensured traceability in data reporting.
Research Associate
ReCode Therapeutics
10.2021 - 12.2022
- Produced LNP-encapsulated RNA for in vitro and in vivo pre-clinical studies, supporting late-phase product development.
- Optimized formulation methods and generated Standard Operating Procedures (SOPs), thereby reducing process deviations.
- Validated analytical methods for LNP-mRNA characterization, ensuring compliance with Good Manufacturing Practices (GMP).
- Conducted in-process characterization, including pH, particle size, and encapsulation efficiency measurements.
Research Associate
Genentech
08.2019 - 09.2021
- Analyzed small molecule compounds using Gas Chromatography (GC) and Fourier Transform Infrared (FTIR) spectroscopy.
- Determined drug purity using High-Performance Liquid Chromatography (HPLC), achieving >95% accuracy.
- Troubleshot instruments and interpreted data using Empower and OpenLab software, improving data reliability.
- Communicated research findings to a team of scientists, optimizing resource allocation.
Senior GMP Manufacturing Specialist
CS-BIO
01.2019 - 07.2020
- Developed and optimized HPLC methods for synthetic peptide purification, achieving a >95% success rate.
- Identified target peptide peaks using mass spectrometry, enhancing process efficiency by 10%.
- Ensured compliance with GMP standards and maintained accurate records of purification experiments.
Education
Bachelor of Science - Chemistry
University of California, Merced
Merced, CA01-2018
Skills
- Chromatography: HPLC, UPLC, GC
- Spectroscopy: UV-Vis, FTIR
- Titration Methods: Karl Fischer
- Software: Empower, OpenLab, Excel
- Regulatory Compliance: GLP, GMP, FDA, ICH
- Analytical Method Development & Validation
- Data Analysis & Interpretation
- Cross-Functional Collaboration
Timeline
Formulation Chemist
Eurofins Inc.
10.2023 - 03.2024
Research Associate
ReCode Therapeutics
10.2021 - 12.2022
Research Associate
Genentech
08.2019 - 09.2021
Senior GMP Manufacturing Specialist
CS-BIO
01.2019 - 07.2020
Bachelor of Science - Chemistry
University of California, Merced
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