GMP QC Chemist: HPLC Method Development & Validation

Sacbar; San Carlos, Northern (CA, KY); Hybrid; USD 90,000 - 115,000; Full time

Job summary

Medterials is seeking a QC Analytical Chemist to join a small, specialty pharmaceutical manufacturing and development company. The role focuses on GMP-compliant analytical testing of drug intermediates, mainly by HPLC, with involvement in method development and validation.

The candidate will contribute to equipment and laboratory maintenance and support both QC and R&D initiatives, requiring a chemistry degree and GMP experience; advanced degrees are welcomed for entry-level opportunities.

Qualifications

• Bachelor's degree in Chemistry with at least four years GMP industry experience or Master's degree with at least two years GMP industry experience.
• PhD in Analytical/Physical/Organic/Medicinal/Pharmaceutical Chemistry welcomed for entry-level.
• HPLC experience is required; LCMS experience is a plus.

Responsibilities

• Perform analytical testing of GMP drug intermediates within the QC department.
• Develop, refine, and validate analytical methods.
• Participate in equipment and laboratory maintenance for the analytical department.

Skills

Attention to detail

Time management

Team communication

Troubleshooting

Analytical thinking

Education

Bachelor's degree in Chemistry

Master's degree in Analytical Chemistry

PhD in Analytical/Physical/Organic/Medicinal Chemistry

Tools

HPLC

LCMS

Microsoft Office

HPLC data software

Job description

Medterials is seeking a QC Analytical Chemist to join a small, specialty pharmaceutical manufacturing and development company. The role focuses on GMP-compliant analytical testing of drug intermediates, mainly by HPLC, with involvement in method development and validation.

The candidate will contribute to equipment and laboratory maintenance and support both QC and R&D initiatives, requiring a chemistry degree and GMP experience; advanced degrees are welcomed for entry-level opportunities.