Quality Supervisor
Listed on 2026-10-09
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Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Management
Regulatory Compliance Specialist
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Quality SupervisorFull-Time Alachua, FL, US
Salary Range: $70,000.00 To $85,000.00 Annually
Location: Alachua, FL
Annual Bonus Opportunity up to $8,000
Evergen is a global industry-leading contract development and manufacturing organization (CDMO) in regenerative medicine. As the only regenerative medicine company that offers a differentiated portfolio of allograft and xenograft biomaterials at scale, Evergen is headquartered in Alachua, FL, and has manufacturing facilities in West Lafayette, IN;
Eden Prairie and Glencoe, MN;
Neunkirchen, Germany;
Glasgow, UK; and Marton, New Zealand.
We are proud to be Great Place to Work Certified in 2026
, reflecting our commitment to creating an exceptional employee experience and workplace culture. Evergen currently has full‑time career opportunities available across multiple locations.
- Paid Time Off (PTO)
- 401(k) with up to a 6% company match
- Holiday pay
- Medical, dental, and vision insurance
- Short-term and long-term disability coverage
- 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. Pa
- 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
Certification
N/A
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
Travel
- N/A
SAFETY
Physical Requirement
- Move or lift objects up to 25 pounds
- Frequent (>75%) stationary position (standing or sitting) while utilizing digital displays
- Frequent (>75%) fine…
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