Bethany Stewart
QA Manager of Analytical Services at Corden Pharma - A Full-Service CDMO
- Role
- Qa Manager of Analytical Services at Corden Pharma - A Full-Service CDMO
- Location
- Longmont, CO, US
- LinkedIn followers
- 500 followers
About Bethany Stewart
With 20 years of experience in Pharmaceutical Chemistry, I have learned a lot. I began my career as a QC Chemist running stock methods for stock products in large Pharma. I have since moved through the ranks into CRO companies. I have enjoyed working with clients first as a bench chemist, then into project management, and then following into personnel management for the projects guiding development, validation, and post-validation activities. I managed teams focused on IVRT/IVPT for product development, SUPAC-SS, and Semi-solid BA/BE comparisons.Most recently, I have transitioned into Quality Assurance for Corden Pharma where I have been learning so much about Active Pharmaceutical Ingredient development and commercial processes. In this role with the Development Products team, I get to walk APIs from phase I through phase GMP analytical and manufacturing processes. This has been such a wonderful learning experience and I’m excited to see where Corden will go!In my personal time, I enjoy spending time with my family. I love my husband and children. I feel blessed for all I have been given.
Experience
Qa Manager of Analytical Services
Corden Pharma - A Full-Service CDMO
Nov 2023 — Present · Boulder, CO, US
Support our ARD and QC teams in review of all analytical review and approval in QA.
Education
East Carolina University
Bachelor's Degree, BS in Biology w/ Minor in Chemistry
1998 — 2001
Skills
- Hplc
- Peer Reviews
- U.s. Food and Drug Administration (Fda)
- Ivrt
- Validation
- Technical Writing
- Lims
- Usp Analyses
- Analytical Chemistry
- Uv/Vis Spectroscopy
- Technology Transfer
- Chromatography
- Troubleshooting
- Karl Fisher
- Standard Operating Procedure (Sop)
- Analytical Method Validation
- Pharmaceutical Industry
- Sop
- Change Control
- Ivrt for Supac-Ss
- Fda
- Lod
- Glp
- Chemistry
- 21 Cfr Part 11
- Uv/Vis
- Pharmaceutics
- Ivrt for Ba/Be
- Laboratory Skills
- Biotechnology
- Laboratory Information Management System (Lims)
- Dissolution
- Capa
- High-Performance Liquid Chromatography (Hplc)
- Quality Control
- Gmp
- Gas Chromatography
- Uv
- Laboratory
- Dissolution Testing
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