Demo

MANAGER, QUALITY ASSURANCE

LGM Pharma, LLC
Taylor, MS Full Time
POSTED ON 4/17/2026
AVAILABLE BEFORE 6/16/2026

RESPONSIBILITIES:

  • Supervise the daily activities in the warehouse to ensure efficient flow of materials and timely completion of Quality Assurance duties.
  • General oversight of systems for labeling, GMP training, compliance, document control, information tracking, and equipment calibration.
  • Lead investigation activities perform root-cause analyses and develop corrective and preventative action plans.
  • Assist in internal and external audits and inspections.
  • Develop and maintain appropriate document storage and retrieval systems.
  • Assist with the review and approval for original and/or revised Quality Operation Processes, and GMP documentation.
  • Use of statistical process control to evaluate trends and provide periodic KPI trend reports to senior management as required.
  • Assure timely closure of audit items. 
  • Provide reports from QA and data to support other business functions, as needed.
  • Ensure Deviations, CAPA and Change Controls are managed in a timely manner.
  • Support the customer complaint process and respond to Customer complaints as required.
  • Performs other related duties as required.
  • Supervise and mentor junior staff members and other related duties as required.
  • Comply with cGMP regulations and all standard operating procedures.

QUALIFICATIONS:

  • Bachelor’s degree in a scientific discipline.
  • 10 years of experience in Quality Assurance in a GMP regulated manufacturing environment, or equivalent combination of education and experience.
  • 5 years of experience leading or supervising others in a GMP regulated manufacturing and distribution environment preferred.
  • Ability to read and interpret technical procedures, SOP’s, GMP’s and governmental regulations.
  • Strong communication skills, both written and verbal.
  • Ability to organize, prioritize and effectively perform concurrent tasks with minimal supervision.
  • Strong attention to detail.
  • Experience in ICH Q7, 21 CFR Part 11, 21 CFR 210 and 211 
  • ASQC quality certifications, ISO 9000 or other Audit training preferred.

Salary : $95,000 - $110,000

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