Senior
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
Experience & Educational Background
Required Qualifications:
OR
Preferred:
Laboratory/manufacturing quality management experience
Regulatory inspection representation experience
Multiple QMS experience (ISO 17025, ISO 9001, GLP, GMP)
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)
Sign up to apply and find out right away if you're a fit.
Your agent will tell you — in seconds.
Sign up and I'll tell you right away how well Bureau Veritas Group matches you — what you already have, and what's missing. Then I stay on it: I search for you and only write when I find something worth your time.