We have an open QC CHEMIST III position in our Quality Control Department in the Irvine, CA location.

PRIMARY DUTIES AND RESPONSIBILITIES:

• Perform and/or assist with analytical testing of raw materials, in-process samples, and finished products.
• 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.

QUALIFICATIONS:

• 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.

At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.