Quality Supervisor
Evergen
Summary
Education: High School Diploma or equivalent
Job description
Responsibilities
- Oversees daily Quality Control operations, ensuring timely review, inspection, and release activities while balancing customer commitments, departmental priorities, and business objectives
- Develops, monitors, and communicates area performance metrics, trends, and key performance indicators (KPIs) to drive accountability, operational visibility, and continuous improvement
- Responsible for effective resource planning by identifying capacity constraints, operational risks and future resource requirements to support projected increases in production volume and organization growth
- Lead the development, implementation, and maintenance of Quality Control processes, procedures, systems, and workflows to improve efficiency, record keeping practices, and scalability
- Supervises and encourages personnel through coaching, performance management, succession planning, training, and employee development
- Leads investigations related to quality events, nonconformances, and process deviations by facilitating root cause analysis and implementing effective corrective and preventive actions through cross-functional collaboration
- Partners with Manufacturing, Quality Assurance, Engineering, Logistics, and other stakeholders to remove operational barriers, improve throughput, and optimize movement of product through the quality system
- Oversees personnel management including scheduling, staffing, PTO management, workload prioritization, and cross-training to ensure business continuity and promoting employee wellness
- Supports internal audits, regulatory inspections, customer audits, and compliance activities by ensuring records, documentation, and processes maintain inspection readiness
- Conducts regular team meetings, performance reviews, and operational planning sessions to align personnel with business objectives, department goals, and customer requirements
- Other duties as assigned
Requirements
Education: High School Diploma or equivalent
Experience: 3+ years of experience in quality in a regulated environment; 2+ years of direct leadership or supervisory experience
Skills: Excellent verbal and written communication; Microsoft Office Suite, intermediate Excel; Proficient in Enterprise Resource Planning (ERP) software; Process Improvement Methodologies; Project Management; Proficient in Quality Management System (QMS) software; Aseptic Technique and Sterile Consciousness; Recognizes variables that could affect test results
Requirements
- High School Diploma or equivalent
- 3+ years of experience in quality in a regulated environment
- 2+ years of direct leadership or supervisory experience
- Excellent verbal and written communication
- Microsoft Office Suite, intermediate Excel
- Proficient in Enterprise Resource Planning (ERP) software
- Process Improvement Methodologies
- Project Management
- Proficient in Quality Management System (QMS) software
- Aseptic Technique and Sterile Consciousness
- Recognizes variables that could affect test results
Benefits
- Paid Time Off
- 401(k) with 6% match
- Holiday pay
- Medical insurance
- Dental insurance
- Vision insurance
- Short-term disability
- Long-term disability
- Paid parental leave
- Annual bonus up to $8,000
Company overview
Evergen is a leading global Contract Development and Manufacturing Organization (CDMO) specializing in regenerative medicine solutions. Founded in 1998 and headquartered in Alachua, Florida, the company operates as a strategic partner to Original Equipment Manufacturers (OEMs) across multiple medical specialties including plastic and reconstructive surgery, sports medicine and orthopedics, neuro/spine, and cardiac applications. Evergen distinguishes itself as the only regenerative medicine CDMO offering a comprehensive portfolio of both allograft and xenograft biomaterials at scale, providing customers with unbiased, needs-driven solutions. The company maintains over 280,000 square feet of cutting-edge medical device manufacturing space worldwide, featuring Class 5-7 clean rooms and Class III PMA-ready facilities. With ISO 13485 certification and FDA/USDA registration, Evergen delivers end-to-end services spanning research and development, regulatory support, manufacturing, and supply chain management. The company's patient-first approach focuses on developing customized biomaterial solutions that promote healing, accelerate recovery, and prevent complications, positioning Evergen as a trusted partner in advancing regenerative medicine technologies.