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Quality Supervisor

Evergen

Alachua, FLOnsitePosted 38 days ago$70,000 - $85,000/year
Full TimeMid LevelQuality (QA / QC)CDMO
Original posting ↗

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.

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