Quality Systems Supervisor

Evergen

Florida

On-site

USD 70,000 - 80,000

Full time

2 days ago
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Benefits offered by this job

Paid Time Off (PTO)
401(k) with company match
Holiday pay
Medical, dental, and vision insurance
Short-term and long-term disability

Job summary

Evergen, located in Alachua, FL, is seeking a Quality Systems Supervisor to oversee critical quality programs and ensure regulatory compliance. The role involves leading a team, coordinating audits, and driving process improvements within a robust quality management framework.

The ideal candidate will have 3+ years in QA/regulatory fields, 2+ years in leadership, and an Associate’s degree. On-site position with comprehensive benefits and a fixed salary range of $70,000–$80,000 per year, plus a

Qualifications

  • Associate’s degree required.
  • 3+ years of quality assurance, systems, regulatory affairs, or related experience in a regulated industry such as tissue, medical device, or pharmaceutical.
  • 2+ years of leadership experience.
  • Alternative combinations of education and experience may be considered.

Responsibilities

  • Oversees and executes functions within critical Quality Systems programs to ensure compliance with applicable regulations, standards and company objectives.
  • Supports quality system compliance with internal and external regulatory requirements and maintains awareness of the regulatory landscape.
  • Collects, analyzes, and reports data to demonstrate conformity and maintains effectiveness of the quality management system.
  • Supports process improvement initiatives that impact quality systems and collaborates with cross-functional stakeholders to ensure compliance of processes and procedures.
  • Supports third-party audits, including Notified Body inspections, through planning, execution, closeout, and follow-up with high customer service.
  • Acts as a subject matter expert during audits for responsible processes.
  • Reviews and approves quality system documentation for accuracy and consistency.
  • Delivers training on responsible processes.
  • Coordinates and leads daily team activities and performance management, hiring, scheduling, corrective actions, and other employee relations issues.
  • Maintains records management system including secure storage, retrieval, retention, and destruction.

Skills

Verbal and written communication
Microsoft Office
QMS software
Problem solving
Data analysis
Records management

Education

Associate’s Degree

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Quality Systems Supervisor

Alachua, FL, US

Salary Range: $70,000.00 To $80,000.00 Annually

Location: On Site, 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; 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 company match
  • Holiday pay
  • Medical, dental, and vision insurance
  • Short-term and long-term disability coverage
  • Oversees and executes functions within critical Quality Systems programs to ensure compliance with applicable regulations, standards and company objectives, including, but not limited to, Document Control and Change Management.
  • Supports quality system compliance with the appropriate internal and external regulatory requirements and maintain awareness of the overall regulatory landscape.
  • Collects, analyzes, and reports data elements to demonstrate conformity and maintains effectiveness of the quality management system with a high degree of accuracy.
  • Supports company process improvement initiatives that impact quality systems and works collaboratively with cross-functional stakeholders to ensure compliance of processes and procedures within the quality management system.
  • Support third-party audits, including Notified Body inspections, through audit planning, execution, closeout, and follow-up with a high level of customer service.
  • Acts as a subject matter expert during internal and third-party audits for responsible processes.
  • Reviews and approves quality system documentation for accuracy, consistency and compliance.
  • Delivers training on responsible processes.
  • Coordinates and leads daily team activities and performance management, hiring, scheduling, corrective actions, and other employee relations issues.
  • Maintains records management system including secure storage, retrieval, retention, and destruction.
  • Other duties as assigned
REQUIREMENTS
Education
  • Associate’s Degree
Experience
  • 3+ years of experience in quality assurance, systems, regulatory affairs, or other relevant experience within a regulated industry such as tissue, medical device, or pharmaceutical.
  • 2+ years of leadership experience
  • A different combination of education and experience may be considered.
Skills
  • Excellent verbal and written communication
  • Microsoft Office suite
  • Quality Management System (QMS) software
  • Problem Solving methodologies
  • Data Analysis
  • Records Management
Travel
  • Minimal travel required, may occasionally travel for professional development or to support company initiatives.
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.)
  • Onsite: Office environment with assigned workstation
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.

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