Elisabeth (Liz) Powers
Manager, Analytical Consulting, CMC Development and Program Management@ Syner-G BioPharma Group
Greater Boston
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Elisabeth (Liz) Powers is an analytical chemist with over 21 years of experience in the pharmaceutical industry. She has expertise in analytical chemistry, drug development, and clinical trials. Elisabeth is skilled in using various analytical techniques and has a strong ability to solve complex drug development problems. She is independent, motivated, and organized, with excellent collaboration and interpersonal skills. Elisabeth has a proven track record of delivering innovative strategies and has successfully managed pre-IND stages to commercial manufacturing. She is also experienced in program management and has a strong ability to coordinate with internal and external quality assurance teams.
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Emails and Phone Numbers

@synergpharma.com
+1 617559****
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About

Analytical chemist with expertise in a wide variety of instrumentation and analytical techniques. Demonstrated ability to solve complex drug development problems through critical thinking and innovative strategies. Independent, motivated and organized with the ability to be flexible and adaptable in a fast-paced, dynamic environment. Excellent collaboration and interpersonal skills, as well as project management experience. Core Competencies: - Experienced in analytical instrumentation such as HPLC (SEC, ELSD, fluorescence, fraction collection, Chem station/Open lab and Empower software) , as well as LC-MS, GC, KF, UV-vis, IR, DSC, XRPD, viscosity, dissolution, and biorelevant dissolution, used to conduct method development and analysis of complex drug substances and drug products to support formulation and process development. - Proficient in experimental design and execution as well as leadership for the analytical development and support of pre-IND stage to commercial manufacturing for a variety of drug candidates including small molecules, peptides and polymers. - Management of specification, reference standard and stability programs for small molecule and peptide compounds in various stages of development both in-house and through CRO management which includes good documentation practices, coordination with internal and external quality assurance (QA) and cross functional development teams. - Authored drug substance sections, reviewed other CMC sections for small molecule IND submissions. -Authored, reviewed and verified data for many supporting documents and reports for a peptide molecule NDA submission. Served as a program manager for a small molecule drug program during early development, IND preparation and filing, and FIH study. - Program management experience and analytical lead positions have allowed demonstration of excellent written and oral communication skills, collaboration and leadership on cross-functional teams to solve complex problems and meet ambitious timelines in a fast paced, dynamic setting. -Active in optimizing lab safety and efficiency, member of the internal HAZMAT spill-response team for 10 years, incident commander level for five years as well as being an evacuation captain for building evacuations

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Work Experience

100 Pennsylvania Avenue, Framingham, MA, 01701, US

Pharmaceutical Manufacturing

219
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Elisabeth (Liz) Powers's Professional Milestones

  • Analytical Chemist | Quality Control (2002-04-01~2006-12-01): Implementing quality control measures to ensure consistent product quality and exceed customer expectations.
  • Scientist | Analytical Development (2019-04-01~2019-09-01): Curating advanced analytical products that revolutionize the field and drive scientific advancements.
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Education

Harvard Extension School
Harvard Extension School

Biotechnology,

Bioengineering,

Nanotechnology,

Master Of Liberal Arts,

Masters,

Nanotechnology And Bioengineering

2010-2016
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