Pavimol Angsantikul
Pharmaceutical Senior Scientist | Formulation Lab Head | Drug Product and Process Development
- Role
- Pharmaceutical Development Scientist and Formulation Lab Head at Population Council
- Location
- Scarsdale, NY, US
- LinkedIn followers
- 500 followers
About Pavimol Angsantikul
I am a pharmaceutical development scientist and formulation lab head of the Angsantikul Laboratory at the Population Council, a global non-profit organization that conducts research and develops solutions to improve sexual and reproductive health and rights. With over 10 years of experience in pharmaceutical science and biomedical engineering, I have established a formulation laboratory that conducts preclinical and early clinical biological drug product development for sexual and reproductive health interventions, following GxP and ICH guidelines. I serve as drug product lead and collaborate with analytical, preclinical, and RAQA teams to underpin in vitro and in vivo safety, PK/PD studies, and regulatory submissions. My core competencies include pre-formulation, formulation, characterization, manufacturing, and stability of novel biological formulations following ICH guidelines and the design and coordination of preclinical studies. I also have expertise in biomimetic nanomedicine, mucosal tissue interfacing, and integration of nano/micro-scale and macro-scale drug delivery systems. My mission is to apply engineering designs to develop innovative and effective delivery systems that address unmet needs and challenges in pressing global health.
Experience
Pharmaceutical Development Scientist and Formulation Lab Head
Sep 2020 — Present
Established a new formulation team and supported people development to advance biologics drug products through preclinical and early clinical development.• Built and led a team to conduct pre-formulation, formulation, and characterization of novel biological formulations• Designed manufacturing process for tray lyophilization to achieve targeted product attributes• Designed and led stability studies of biological drug products following ICH guidelines• Collaborated with analytical team to develop and validate UPLC method for biological drug substance and drug product• Coordinated with preclinical teams to provide biological drug products for in vitro and in vivo safety, PK/PD studies• Regularly communicated with RAQA team to ensure smooth translation of drug products to early clinical stage• Authored and reviewed regulatory and technical documents, study reports, and manuscripts
Education
Chulalongkorn University
Bachelor's degree, Nano Engineering
2008 — 2012
UC San Diego
Doctor of Philosophy - PhD, NanoEngineering
2013 — 2018
Harvard University
Postdoctoral Research Fellow, Bioengineering and Biomedical Engineering
2018 — 2020
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