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For your reference, we have included the original job posting below.
Research Scientist II - DMPK - Req. Code : 904
Job Number:
35603051
Company Name:
AMRI Global
Job Location:
Albany, NY US
Job Category:
Science & Biotech
Research Scientist II - DMPK - Req. Code : 904
Research Scientist II - DMPK - Req. Code : 904
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Open Date 7/20/2011
Job Title Research Scientist II - DMPK
Education Bachelor's Degree
Location Albany, NY Albany, NY 12203, US
Career Level Experienced (Non-Manager)
Category Chemistry R&D
Date Needed By N/A
Job Type Scientific Full Time
Travel Required 0
Job Description
The Research Scientist II is an experienced scientist in the field of ADME-Toxicology and bioanalytical experimentation. The principal responsibility of the Research Scientist II is to execute internal and external projects in the areas of ADMET and bioanalysis using a variety of in vitro experiments. The Research Scientist II is expected to demonstrate facility in both the theoretical and practical aspects of ADMET assays and analytical chemistry. Major components in the scientist's performance rating will be based on productivity, intellectual input, and ability to work independently. Timely delivery of in vitro ADME-Toxicology data to support internal and external projects. Particular focus on bench execution of ADMET assays with ability to cross train for bioanalytical assays. Apply a wide range of analytical techniques to analyze and characterize results of ADMET assays. Develop and maintain a working knowledge of commonly used spectroscopic and chromatographic procedures. Design and conduct ADMET studies using manual or automated platforms, analyze experimental data, and report data electronically and/or in reports and memos. Help monitor the latest developments in specific areas of technical responsibility, and recommend and implement methods to increase the quality of products and services. Advice and/or train scientists for the efficient conduct of ADMET ibit safety awareness and safe work practices and maintain familiarity with the Chemical Hygiene Plan. Process samples with the standard procedures effectively with supervision, including analysis of experimental data for validity before reporting results. Keep contemporary, accurate, legible, and complete experimental records in accordance with GLP mit complete, documented, and legible reports of testing. Ensure that data is properly filed and accessible for review in accordance with appropriate SOP'age workload and time to perform multiple projects effectively, and ensure all necessary paperwork is completed on a timely basis. Participate in self-development activities and training of form other related duties as may be reasonably assigned in the course of business.
# of Openings 1
Job Requirements
· B.S. or M.S. Degree in Biochemistry, Biology, Pharmaceutical Science, Chemistry or a related field with experience in ADME/Toxicology assay execution and development, or in closely related C or HPLC/MS experience is wledge of basic laboratory procedures, such as pipetting, concentration calculations, and preparation of buffers and solutions. Computer training in the use of standard office software applications and databases
