MANAGER, QUALITY ASSURANCE

LGM Pharma LLC

Taylor, MS

JOB DETAILS
SKILLS
Business Support, Calibration, Change Control, Code of Federal Regulations, Communication Skills, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Current Good Manufacturing Practice (cGMP), Customer Support/Service, Detail Oriented, Distribution Services, Document Control, Documentation, Establish Priorities, External Audit, GMP (Good Manufacturing Practices), Government Regulations, ICH Regulations, ISO 9000, Internal Audit, Leadership, Manufacturing, Mentoring, Operations Processes, Performance Metrics, Presentation/Verbal Skills, Quality Assurance, Quality Management, Regulations, Reporting Skills, Root Cause Analysis, Standard Operating Procedures (SOP), Statistical Process Control, Time Management, Track Customer Issues, Trend Analysis, Warehousing, Writing Skills
LOCATION
Taylor, MS
POSTED
30+ days ago

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.

About the Company

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LGM Pharma LLC