Bree Discar
Erie,CO
Summary
Extensive experience in client-facing technical roles in pharmaceutical development. Strengths include technical writing and data presentation, process improvement, and project management.
Overview
8
8
years of professional experience
Work History
Scientist I
Cambrex
11.2020 - Current
- Pre-formulation characterization and formulation development of pharmaceutical candidates.
- Generate written reports for experimental results and development progress.
- Present weekly technical updates to clients.
Pharmaceutical Chemist II
Catalent
03.2020 - 11.2020
- Formulation development of injectable drug products and technical transfer to manufacturing sites.
- Responsible for writing protocols and test methods.
- Generated development reports and presented updates to clients.
Associate Quality Engineer
Catalent
09.2018 - 03.2020
- Founded deviation management group for the site to establish processes for root cause analysis and deviation documentation.
- Facilitated cross-departmental investigations and corrective actions.
- Primary technical writer for all analytical OOS/OOT deviations and investigations.
- Managed progress for all open records to ensure on-time closure.
Quality Control Chemist
Catalent
04.2017 - 09.2018
- Executed analytical testing under cGMP guidelines.
- Participated in writing and reviewing SOPs.
Education
B.S. - Physiology and Neuroscience
University of California San Diego
06-2016
Skills
- Technical Writing
- Client Communication
- Data Presentation
- Project Management
- Analytical Chemistry
- Formulation Development
Publications
"Circadian Regulation of Metabolism in Health and Disease" (pp. 443-458) in Biological Timekeeping: Clocks, Rhythms, and Behaviour (2017)
Timeline
Scientist I
Cambrex
11.2020 - Current
Pharmaceutical Chemist II
Catalent
03.2020 - 11.2020
Associate Quality Engineer
Catalent
09.2018 - 03.2020
Quality Control Chemist
Catalent
04.2017 - 09.2018
B.S. - Physiology and Neuroscience
University of California San Diego
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