QC CHEMIST III

LGM Pharma, LLC • Irvine, CA

6d • $30 - $35 • Onsite

About The Position

We have an open METHOD VALIDATION / ANALYTICAL CHEMIST III position in our Quality Control Department in the Irvine, CA location.

Requirements

• Bachelor's degree in chemistry or related discipline.
• 5+ years' experience in a chemistry laboratory, or equivalent combination of education and experience.
• 5+ years' experience with analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, and dissolution apparatus required.
• 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.

Nice To Haves

• 2+ years' experience in GLP or GMP (preferred) environment.

Responsibilities

• Perform method validation, verification, transfer, analytical testing for clinical submission materials, including raw materials, finished products, stabilities and cleaning validation.
• Maintain and troubleshoot analytical instrumentation.
• 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.
• Other related duties as required.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level