Quality Assurance Lead

Overview Business Title: Quality Assurance Lead Position Title: Quality Assurance Specialist V Division: Consumer Products Services Entity: Galbraith Laboratories Reports to: Sr Manager, QHSSE FLSA: Exempt Location: Knoxville, TN Hours Worked: Typically, Monday through Friday, 40 per week However, must be flexible to meet the needs of the department and complete other projects as assigned. Major Roles & Responsibilities External Representation & Regulatory Affairs Lead customer audits independently, and support QA Manager for regulatory inspections & agency visits Draft audit responses and corrective action plans Monitor regulation changes, assess risk, and close compliance gaps Assist with facilitating scope expansion with regulating/certifying bodies Strategic Management Participate in cross-departmental corrective activities based on trends Support quality event trending and corrective actions Facilitate cross-departmental communication Improve efficiency and effectiveness of quality processes Reporting & Oversight Assist in preparing Management Review Meeting reports Report quality systems status to QA Manager Develop tracking/trending tools and communicate trends to leadership Collaborate with managers on company policies, goals, and procedures Advanced Technical Authority Oversee CAPA system Ensure departmental priorities, goals, and policies are met Oversee Quality Assurance Unit policies/procedures Approve/reject procedures and specifications for data/client reports Review and approve investigations, deviations, and change controls Direct inspections and audits for materials, facilities, and test results Advise Quality Manager on regulatory strategy and developments Client Relations Resolve client issues to enhance satisfaction Lead client audits Track deviations, change controls, and complaints Knowledge, Skills & Abilities Core Competencies Leadership: Lead, develop, and motivate QA teams Communication: Exceptional written/verbal skills for executive reporting and stakeholder engagement Regulatory Expertise: Deep understanding of requirements and proactive compliance management Technical Proficiency: Advanced knowledge of QMS, statistical analysis, and validation Technical Skills Expertise in QMS implementation and continuous improvement Thorough understanding of ISO 9001, 17025, CFR 210, 211, 820 Proficient in quality data analysis, trending, and reporting Advanced proficiency with QMS software, databases, and statistical tools Expert knowledge of GLP, GMP, and regulatory frameworks Management & Leadership Train and develop QA team on data analysis and quality management Strong interpersonal and relationship-building skills Oversee large, cross-departmental projects Excellent project management and coordination skills Analytical & Problem-Solving Advanced problem-solving for complex quality challenges Manage multiple high-priority projects simultaneously Expertise in root cause analysis and corrective action implementation Strong attention to detail with strategic perspective Additional Competencies Organizational and time management excellence Proactively interpret and apply new regulations Positive attitude, self-motivated, highly engaged Proficiency with Windows, Word, Excel, and specialized quality software Required Qualifications Experience & Educational Background Bachelor's Degree + 7 years QA experience with progressive responsibility OR Master's Degree + 5 years QA experience with progressive responsibility Preferred Laboratory/manufacturing quality management experience Regulatory inspection representation experience Multiple QMS experience (ISO 17025, ISO 9001, GLP, GMP) Compensation Compensation Range: $75,000 - $90,000 annually (e.g., the job posting is not necessarily reflective of actual compensation that may be earned, and actual compensation is subject to variation due to such factors as locations, education, experience, and skillset) #J-18808-Ljbffr RXinsider LTD.