Quality Manager III

Location: Morristown, TN

Company: Iatric Manufacturing Solutions

About Us

At Iatric Manufacturing Solutions, we’re dedicated to fostering healthier environments by producing FDA-regulated wipes for consumer, healthcare, food service, and hospitality industries. As a privately held company, we combine innovation with integrity to deliver products that make a difference. Our culture is built on our RRITE values: Renew, Respect, Integrity, Teamwork, and Excellence—principles that guide everything we do.

What You’ll Do

As a Quality Manager III, you will lead our Quality Assurance function and ensure that every product meets stringent regulatory and internal standards. You’ll oversee Quality Assurance, Quality Control, Laboratory, Quality Systems, and Quality Engineering teams, driving compliance and continuous improvement across the organization.

Key Responsibilities

• Lead and develop Quality teams through hiring, training, and performance management.
• Ensure compliance with FDA regulations (21 CFR Parts 210, 211, 820), ISO standards, and global requirements.
• Oversee Quality Management System (QMS) and strategic quality initiatives.
• Manage batch record reviews, validation reporting, NC/CAPA investigations, and change control activities.
• Drive process improvements, validation activities, and new product commercialization.
• Build strong relationships with customers and suppliers to resolve quality issues and support new product launches.
• Lead internal and external audits and implement corrective actions.
  
  

What We’re Looking For

• Education: Bachelor’s degree in Science, Engineering, or related technical discipline.
• Experience: Minimum 10 years in Quality Assurance Management within an FDA cGMP-regulated manufacturing environment (Pharmaceutical/OTC Drug/Medical Device experience preferred).
• Expertise: Strong knowledge of 21 CFR compliance, cGMP, ISO 13485, HACCP/FMEA, auditing, risk management, SPC, DOE, and validation processes.
• Preferred Certifications: ASQ Certified Quality Auditor/Engineer, Certified Pharmaceutical cGMP Professional, or Regulatory Affairs Professional Certification (RAPS).
• Proven leadership in Quality Engineering and Quality Control.
  
  

Why Join Iatric?

• Impact: Play a critical role in ensuring product safety and compliance in industries that matter.
• Culture: Work in an environment that values integrity, teamwork, and continuous improvement.
• Growth: Opportunities for professional development and leadership in a growing organization.
• Innovation: Be part of a company that invests in technology and quality to deliver best-in-class products.
  
  

Benefits At Iatric

We offer a comprehensive benefits package designed to support your health, financial security, and work-life balance, including:

• Health & Wellness: Medical, dental, vision coverage, wellness programs, and fitness reimbursement
• Financial Security: Retirement savings with company match, life and disability insurance, and optional supplemental coverage
• Career & Lifestyle: Paid time off, education reimbursement, and employee discount programs
• Mental Health Support: Confidential counseling and resources for personal and work-life needs
  
  

Ready to make an impact?

Join a team where your expertise in quality and compliance helps create products that protect health and safety across industries. At Iatric, you’ll lead meaningful projects, collaborate with passionate professionals, and drive innovation in a fast-paced, FDA-regulated environment. Your work will make a difference—every day.