SENIOR QC CHEMIST

LGM Pharma, LLC•Rosenberg, TX

About The Position

PRIMARY DUTIES AND RESPONSIBILITIES: Perform routine and non-routine chemical analysis of raw materials, in-process samples, and finished products using validated analytical methods. Operate and maintain laboratory instrumentation such as HPLC, GC, UV-Vis, FTIR, and other analytical equipment. Review and interpret analytical data to ensure compliance with specifications and regulatory requirements. Troubleshoot analytical methods, instrumentation issues, and laboratory processes. Develop, validate, and transfer analytical methods in accordance with industry standards (e.g., USP, ICH, FDA guidelines). Prepare and review laboratory documentation, including test methods, protocols, reports, and SOPs. Ensure all laboratory activities comply with cGMP, safety, and company policies. Train and mentor junior chemists and laboratory technicians. Support internal and external audits and inspections. Maintain accurate and timely documentation in laboratory systems (e.g., LIMS, notebooks). Collaborate with cross-functional teams, including Quality Assurance, Production, and R&D. Assist with investigations related to out-of-specification (OOS) and out-of-trend (OOT) results. QUALIFICATIONS:

Requirements

Bachelor’s degree in chemistry or related scientific field required; Master’s degree preferred.
Minimum of 5+ years of experience in a pharmaceutical or GMP-regulated laboratory.
Strong knowledge of analytical techniques such as HPLC, GC, and spectroscopy.
Familiarity with cGMP, FDA, USP, and ICH guidelines.
Strong analytical, problem-solving, and organizational skills.
Ability to work independently and manage multiple priorities.
Excellent written and verbal communication skills.

Responsibilities

Perform routine and non-routine chemical analysis of raw materials, in-process samples, and finished products using validated analytical methods.
Operate and maintain laboratory instrumentation such as HPLC, GC, UV-Vis, FTIR, and other analytical equipment.
Review and interpret analytical data to ensure compliance with specifications and regulatory requirements.
Troubleshoot analytical methods, instrumentation issues, and laboratory processes.
Develop, validate, and transfer analytical methods in accordance with industry standards (e.g., USP, ICH, FDA guidelines).
Prepare and review laboratory documentation, including test methods, protocols, reports, and SOPs.
Ensure all laboratory activities comply with cGMP, safety, and company policies.
Train and mentor junior chemists and laboratory technicians.
Support internal and external audits and inspections.
Maintain accurate and timely documentation in laboratory systems (e.g., LIMS, notebooks).
Collaborate with cross-functional teams, including Quality Assurance, Production, and R&D.
Assist with investigations related to out-of-specification (OOS) and out-of-trend (OOT) results.