Senior Analytical Chemist - HPLC Method Validation (GMP)

Xseerpharma; Los Angeles (CA); Hybrid; USD 100,000 - 130,000; Full time

Job summary

Xseer Pharmaceuticals in Los Angeles is seeking a hands-on Senior Analytical Chemist with strong HPLC experience to join the Quality Control team. The role focuses on validating HPLC methods and documenting activities in line with cGMP and approved procedures.

You will work closely with the Associate Director of Chemistry to perform method validation, review data, maintain records, and support routine testing of in-house API materials and finished products.

Qualifications

• Minimum of three years of hands-on HPLC experience.
• Experience in a pharmaceutical or similarly regulated cGMP laboratory.
• Strong attention to detail and the ability to maintain accurate and complete lab documentation.

Responsibilities

• Perform HPLC analytical method validation for a variety of pharmaceutical compounds.
• Execute validation protocols and document procedures, calculations, results, deviations, and conclusions.
• Review chromatographic data, system suitability results, and calculations for accuracy.
• Prepare and maintain laboratory records per cGMP, SOPs, and test methods.
• Communicate testing progress, technical issues, and results to supervision.

Skills

HPLC

Analytical Chemistry

Documentation

Communication

Independent work

Education

Bachelor's degree in Chemistry or related field

Job description

Xseer Pharmaceuticals in Los Angeles is seeking a hands-on Senior Analytical Chemist with strong HPLC experience to join the Quality Control team. The role focuses on validating HPLC methods and documenting activities in line with cGMP and approved procedures.

You will work closely with the Associate Director of Chemistry to perform method validation, review data, maintain records, and support routine testing of in-house API materials and finished products.