Quality Supervisor

Posted 2 Days Ago
Be an Early Applicant
Alachua, FL, USA
In-Office
70K-85K Annually
Mid level
Medical Devices & Diagnostics
The Role
Supervises daily Quality Control operations in a regulated regenerative medicine manufacturing environment. Oversees inspections, reviews, product release, staffing, training, performance metrics, investigations, root-cause analysis, CAPA implementation, audit readiness, and continuous process improvement. Collaborates with Manufacturing, Quality Assurance, Engineering, Logistics, and other stakeholders to improve quality-system throughput and operational performance.
Summary Generated by Built In

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.

Our comprehensive benefits package includes:

    • 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
    • Paid parental leave and much more!

    Read more about this change and Evergen’s commitment to advancing regenerative medicine here: https://www.linkedin.com/company/evergenbio


    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. 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 manipulation using hands and fingers (typing, opening, writing, clicking, paper sorting, etc.)

    More about Evergen:

     

    Evergen provides customers across a diverse set of market segments with leading-edge expertise, scale, and flexibility across end-to-end services including design, development, regulatory support, verification and validation, manufacturing, and supply chain management. 


    Evergen is rooted in a steadfast commitment to quality, integrity, and patient safety with a focus on five key values:

    • Accountable: We own our actions and decisions.
    • Agile: We embrace change to stay ahead of the curve and evolve to drive innovation and growth. 
    • Growth Mindset: We embrace challenges as opportunities for continuous learning.
    • Customer-Centric: We prioritize customers at every touch point. 
    • Inclusive: We thrive on the richness of our diversity and ensure every voice is heard, respected, and celebrated. 

    At Evergen, we are committed to fostering an inclusive workplace where we embrace the richness of our diversity and ensure that every voice is heard, respected, and celebrated. We believe that by embracing diversity and promoting inclusivity, we not only uphold our values but also strengthen our position as the CDMO of Choice in regenerative medicine solutions. We recognize that cultivating a growth mindset is essential to our success, and we are dedicated to continuous learning and improvement in our diversity, equity, and inclusion efforts. Through accountability and action, we strive to create an environment where individuals can thrive, innovate, and contribute their unique perspectives to drive our collective success.

     

    Montagu Private Equity (“Montagu”), a leading European private equity firm, acquired RTI in 2020 and has supported the transformation of the company to its next level of potential.


    #LI-Onsite

    Skills Required

    • High school diploma or equivalent
    • At least 3 years of experience in quality within a regulated environment
    • At least 2 years of direct leadership or supervisory experience
    • Excellent verbal and written communication skills
    • Microsoft Office Suite proficiency, including intermediate Excel
    • Proficiency in Enterprise Resource Planning (ERP) software
    • Knowledge of process improvement methodologies
    • Project management skills
    • Proficiency in Quality Management System (QMS) software
    • Aseptic technique and sterile consciousness
    • Ability to recognize variables that could affect test results
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    The Company
    HQ: Alachua, Florida
    515 Employees
    Year Founded: 1998

    What We Do

    Evergen is a leading Contract Development and Manufacturing Organization (CDMO) pushing the boundaries of innovation and tissue engineering to meet patient needs in regenerative medicine. We are expert partners to Original Equipment Manufacturers (OEMs), working with them to identify clinical problems and develop customized solutions that promote healing, accelerate recovery, and help prevent complications. Using our extensive portfolio of biological materials, we focus on specialized clinical segments, including plastic and reconstructive surgery, sports medicine and orthopedics, cardiac, and neurosurgery. Our Mission is to enhance patients' lives by creating the best clinical outcomes through innovative, high-quality medical solutions.

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