Clinical and Health - Scientist II - 30.00/hr.

Kelly; High Point (NC); Presencial; USD 65.000 - 85.000; Jornada completa

Descripción de la vacante

Kelly in High Point, NC is seeking an analytical chemist to perform quality control testing on finished products and stability samples using validated methods for strength, impurities and identity. The role includes spectroscopy and chromatography, mainly HPLC and GC, with Empower 3 software support and documentation of results.

The ideal candidate has a BS in science and at least 3 years of chromatography experience in a GMP/FDA-regulated lab, plus proficiency with common office software and

Formación

• Bachelor's degree in Science is required.
• At least 3 years of chromatography experience with HPLC and GC.
• Experience with Empower 3 data acquisition software preferred.
• Experience in a GMP FDA regulated laboratory environment.
• Proficiency with common office software and chromatographic data systems.

Responsabilidades

• Conduct chemical and physical testing of pharmaceutical finished product and stability samples.
• Utilize validated test methods for strength, impurities, identity, spectroscopy, and chromatography, including HPLC and GC.
• Operate chromatography systems and document results accurately.

Conocimientos

HPLC

GC

Empower 3

Educación

Bachelor's degree in Science

Herramientas

HPLC

GC

Descripción del empleo

Conducts chemical and physical testing of pharmaceutical finished product and stability samples by internally developed and compendial test methods. Utilizes validated test methods for pharmaceutical raw materials and finished products for strength, impurities, and identity, spectroscopy, and traditional quantitative analysis, spectroscopy, and/or traditional wet chemical testing as well as chromatography (HPLC and GC).

• Bachelor's degree in Science required. Preferably in Chemistry or Biology.
• A minimum of 3 years chromatography experience with HPLC and GC.
• Experience with Empower 3 data acquisition software preferred.
• Experience in a GMP FDA regulated laboratory environment.
• Experience with common office software and chromatographic data acquisition systems.