Scientist

Integrated Resources, Inc

South Plainfield, New Jersey

JOB DETAILS
JOB TYPE
Contractor
SKILLS
Analysis Skills, Analytical Development, Biotech and Pharmaceutical, Consulting, Current Good Manufacturing Practice (cGMP), Drug Development, Drug Products, Fourier-Transform Infrared Spectroscopy (FTIR), High Performance Liquid Chromatography (HPLC), Mass Spectrometry, Process Development, Quality Assurance Methodology, Requirements Validation/Verification, Research & Development (R&D), Reversed Phase HPLC, Scientific Principles, Securities and Exchange Commission (SEC), Standard Operating Procedures (SOP), Testing, UV/VIS (Ultraviolet-Visible Spectroscopy)
LOCATION
South Plainfield, New Jersey
POSTED
1 day ago
ScientistPosition: ScientistLocation: South Plainfield, NJDuration: Contract to hire (3-6 months contract)Job SummaryScientist II reports to and takes direction from the Associate Director, R&D.Scientist II is knowledgeable in the areas of method development, method validation, and drug characterization.Develop and validate methods for experimental drug candidates.Perform characterization studies for impurities, degradants, intermediates, and active components of drug substances and drug products.Technical experience must include analysis of proteins by HPLC (SEC, RP-HPLC, IEX), electrophoretic techniques (SDS-PAGE, IEF, Western blotting), and spectroscopy (UV and VIS).Write and review method transfer protocols and method SOP'sPerform analytical testing to support process development and release/stability testing.MS or PhD in a scientific discipline or equivalent and 3-4 years related experience; may include post-doctoral experience.Excellent knowledge of scientific principles and concepts.Other special projects and/or duties may be assigned by Management.Biophysical techniques (CD, FTIR, DSC); mass spectrometry (electrospray, MALDI); capillary electrophoresis; peptide mapping; amino acid analysis; protein sequencingWorking knowledge of important aspects of analytical development in the pharmaceutical industry, particularly pertaining to cGMP and method validation requirements

About the Company

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Integrated Resources, Inc