Thermo Fisher Scientific is seeking an Associate Research Scientist in Stability to perform complex laboratory analyses related to pharmaceutical products. The ideal candidate will have a background in analytical chemistry with 6-8 years of experience in a GMP environment, and will be responsible for authoring stability protocols, analyzing data, and ensuring compliance with regulatory standards
Job Summary
As an Associate Research Scientist, you will perform complex laboratory analysis of pharmaceutical products and proficiently use analytical instrumentation, calculate and analyze data and record data in adherence with PPD SOP's and the industry.
This position is in the Stability group in the Analytical Strategy & Operations (ASO) department and is located in New Brunswick, New Jersey.
We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes a choice of national medical and dental plans, and a national vision plan, including health incentive programs.
Matching Summary
Match Score: 85
Thermo Fisher Scientific is seeking an Associate Research Scientist in Stability to perform complex laboratory analyses related to pharmaceutical products. The ideal candidate will have a background in analytical chemistry with 6-8 years of experience in a GMP environment, and will be responsible for authoring stability protocols, analyzing data, and ensuring compliance with regulatory standards.
Salary
Base: $91,700.00–$110,000.00; Bonus/Equity: Variable annual bonus based on performance; Benefits: Comprehensive Total Rewards package including medical, dental, vision, PTO, holidays, parental leave, retirement savings, ESPP
Skills & Requirements
Must-have
Author stability protocols and reports
Adherence to GMP Safety Standards
Proficient in MS Word and Excel
Work under assigned timelines
Communicate regulatory issues
Nice-to-have
Familiarity with electronic documentation systems
Familiarity with laboratory test methods
Interact with clients
Project leader experience
Key Requirements
B.S. or equivalent in Analytical Chemistry, Chemistry, Biochemistry
6-8 years of pharmaceutical industry experience in GMP environment