Senior Analytical Chemist

2 weeks ago

Irvine, California, United States LGM Pharma, LLC Full time
Job Summary

We are seeking a highly skilled QC Chemist A (III) to join our Quality Control Department in Irvine, CA. The successful candidate will be responsible for performing method validation, verification, transfer, and analytical testing for clinical submission materials.

Key Responsibilities:

  • Validate and verify analytical methods for raw materials, finished products, stabilities, and cleaning validation.
  • Maintain and troubleshoot analytical instrumentation, including HPLC, GC, CE, ICP, FTIR, and dissolution apparatus.
  • Perform and document laboratory investigations as necessary.
  • Peer review data generated by other chemists and technicians.
  • Develop, validate, and troubleshoot analytical methods.
  • Conduct method transfers from other facilities and departments.
  • Author standard operating procedures and analytical methods.
  • Perform and/or assist with equipment calibrations and qualification.
  • Assist laboratory management with laboratory employee training.
  • Assist laboratory management in preparation for internal, customer, and agency audits.

Requirements:

  • Bachelor's degree in chemistry or a related discipline.
  • 5+ years' experience in a chemistry laboratory or an equivalent combination of education and experience.
  • 5+ years' experience with analytical instrumentation, including HPLC, GC, CE, ICP, FTIR, and dissolution apparatus.
  • 2+ years' experience in a GLP or GMP environment (preferred).
  • Ability to follow standard operating procedures.
  • Strong communication skills, both written and verbal.
  • Ability to organize, prioritize, and effectively perform concurrent tasks with minimal supervision.
  • Strong attention to detail.

LGM Pharma, LLC is an equal opportunity employer and welcomes applications from all qualified candidates. We are committed to creating a diverse and inclusive work environment.

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