QC Analytical Chemist: GMP Testing & HPLC Method Dev

Califesciences; San Carlos, Northern (CA, KY); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Medterials is seeking a QC Analytical Chemist to perform analytical testing of GMP drug intermediates within a small, specialty pharmaceutical manufacturing and development company.

The role focuses on method development, validation, and routine QC analysis using HPLC, with involvement in documentation, troubleshooting, and collaboration with QC and R&D teams. Strong GMP/GLP practices and data reporting are essential.

Qualifications

• Bachelor’s in Chemistry required; 4+ years GMP industry experience or Master’s in Analytical Chemistry with 2+ years GMP experience.
• PhD candidates may apply with relevant analytical chemistry focus.
• HPLC experience is required; LC-MS is a plus; strong documentation and data analysis skills expected.

Responsibilities

• Perform analytical testing of GMP drug intermediates in QC as part of a small specialty pharma team.
• Develop and refine analytical methods; validate and transfer methods to QC; support R&D efforts as needed.
• Assist in equipment and laboratory maintenance; generate technical reports and troubleshooting documentation.

Skills

Detail oriented

Time management

Troubleshooting

Written technical reports

Education

Bachelor's in Chemistry

Master's in Analytical Chemistry

PhD in Analytical/Pharmaceutical Chemistry

Tools

HPLC

LC-MS

MS Office

Job description

Medterials is seeking a QC Analytical Chemist to perform analytical testing of GMP drug intermediates within a small, specialty pharmaceutical manufacturing and development company.

The role focuses on method development, validation, and routine QC analysis using HPLC, with involvement in documentation, troubleshooting, and collaboration with QC and R&D teams. Strong GMP/GLP practices and data reporting are essential.