W. Paul Findlay, Phd, Pmp Email & Phone Number

Greater New York City Area

Greater New York City Area

Brooklyn, NY

Arnold & Marie Schwartz College of Pharmacy and Health SciencesPHS 761 – QbD and Process Validation: Spring 2018, Spring 2019, Spring 2020, Spring 2021, Fall 2021, Spring 2022, Fall 2022, Spring 2023, Fall 2023, Fall 2024PHS 750 - Pharmaceutical cGMPs: Fall 2019PHS 931 - Advanced Physical Pharmacy I: Spring 2017PHS 932 - Advanced Physical Pharmacy II: Fall.

Greater New York City Area

I was responsible for the transfer of all aspects of drug product manufacture and packaging from one current CMO to three additional CMOs (domestic and international). I reviewed and approved all development plans, validation protocols and manufacturing batch records. I coordinated with project managers and technical scientists at each site to perform.

Greater New York City Area

College of Pharmacy and Health SciencesFall 2016: PAS 268 - Good Manufacturing PracticesFall 2015: PAS 260 - Basic Concepts of Drug DevelopmentSpring 2015: PAS 272 - Process Validation

East Hanover, NJ

I was a consultant brought in to tech transfer four Novartis products (including analytical, manufacturing and packaging) from an internal Novartis manufacturing facility to a CMO. I coordinated the meetings and activities between sites, assured that all specifications, methods, protocols and batch records were successfully transferred, and supported.

Commack, NY

I was a project manager/technical expert for drug product technical transfer teams. As the project manager/technical expert, I ran regular tech transfer meetings, maintained adherence to the Forest technical transfer model, coordinated development timelines, developed and tracked project budgets and managed all aspects of the tech transfer process. I.

Commack, NY

I was in a formulation and process development group, developing and scaling up drug product processes and performing the technology transfer to the commercial site. I coordinated manufacturing activities at the development site and the commercial manufacturing site and evaluated container closure systems for products through stability testing. I have.

New Brunswick, NJ

1. I performed technology transfer of solid dosage form processes from development to full-scale manufacturing and from manufacturing site to manufacturing site. As part of the transfers, the manufacturing processes of the company’s major products were assessed on a routine (i.e. yearly) basis for a process information database.2. I developed methods for.

West Lafayette, IN

New Brunswick, NJ

I was responsible for the analysis of pharmaceutical compounds by IR and Raman spectroscopy and subsequent reporting of results. I developed methods for routine IR identity testing and assays for solid-state polymorphic determinations and used FTIR and FT-Raman spectroscopy and microspectroscopy, hot-stage IR microscopy and diffuse reflectance IR.

St. Louis, MO

I was a bench chemist in the Animal Sciences Division and the Physical Sciences Center. I tested animal, feed and water samples to support projects in the Animal Sciences Division and performed HPLC analysis to support Monsanto's polymeric products in the Physical Sciences Center. I was recognized for my work in developing and implementing a fatty-acid.

Phd, Industrial And Physical Pharmacy

“Near-Infrared Spectroscopic Monitoring of Fluidized Bed Granulation: Process Control and Control of Granule Strength” The objective of.

Education record

Graduate course work in Chemistry.

Ba, Chemistry

Senior Thesis: "Construction and Characterization of a Flash Photolysis Apparatus."