- Added - 03/05/2024
- Perform routine and non-routine chemical analysis tests on raw materials, in-process samples, and finished products following established protocols and SOPs.
- Analyze and interpret test results, ensuring compliance with regulatory standards and specifications.
- Utilize analytical instruments and techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy to conduct tests and analyze samples.
- Maintain and calibrate laboratory equipment, ensuring accuracy and reliability of results.
- Support investigations into out-of-specification results and deviations, identifying root causes and implementing corrective actions.
- Collaborate with cross-functional teams to develop, optimize, and validate analytical methods.
- Monitor and document laboratory activities, including sample preparation, testing, and data analysis, ensuring compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Bachelor's degree in Chemistry or related field.
- 2 years of experience in a pharmaceutical QC laboratory.
- Strong knowledge of cGMP regulations and regulatory requirements.
- Proficiency in operating and troubleshooting analytical instruments such as HPLC, GC, FTIR, and UV-Vis spectroscopy.
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Chemist A
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Chemist
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Formulation Chemist
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QC Chemist - Trenton, United States - Astrix Technology
Description
QC ChemistScience & Research
Trenton , NJ, US
Pay Rate Low: 26.00 |
Pay Rate High: 30.00
Responsibilities
Requirements
INDBH
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.