We have an open position for a Quality Control Chemist B in our Quality Department located in the Irvine, CA location.

RESPONSIBILITIES:

•  Perform and/or assist with analytical testing of raw materials, in-process samples, and finished products.
• Utilize analytical laboratory instrumentation, primarily the HPLC.
• Comply with cGMP regulations and follow all standard operating procedures.
• Peer review data generated by other technicians.
• Maintain and troubleshoot laboratory equipment and analytical instrumentation within level of experience.
• Perform and/or assist with equipment calibrations and qualification.
• Other related duties as required.

QUALIFICATIONS:

•  Bachelor's degree in chemistry or related discipline.
• 2 years’ experience in a pharmaceutical environment, testing small molecules. 
• 2 years’ experience with analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC, MS, and dissolution apparatus.
• 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.

Job Type: Experience 

Schedule: Full-Time 

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.