We have an open position for a QC Chemist II in our Quality Department located in the Rosenberg, Texas facility. 

RESPONSIBILITIES:

• Perform analytical testing of raw materials, in-process samples, finished products and stability samples.
• Maintain and troubleshoot analytical instrumentation.
• Peer review data generated by other chemists and technicians.
• Validate, verify 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 in preparation for internal, customer and agency audits.
• Mentor other chemists on good laboratory practices.
• Other related duties as required.

QUALIFICATIONS:

• Bachelor's degree in chemistry or related discipline.
• 2+ years' experience in a pharmaceutical or analytical chemistry laboratory
• 2+ years' experience with analytical instrumentation ( e.g, HPLC, GC, FTIR).
• 2+ years' experience in GLP or GMP environment.
• 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. We offer a competitive benefit package. 

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.