What are the responsibilities and job description for the Quality Manager III position at Rockline Industries/Iatric?
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’ll play a critical role in ensuring compliance and driving continuous improvement across our Iatric manufacturing operations. You will lead validation activities, mentor quality engineers, and manage risk-based initiatives to uphold the highest standards of quality and safety.
Key Responsibilities:
- Develop and execute validation protocols (IQ/OQ/PQ) for equipment, sanitation, facilities, software, and processes.
- Maintain and ensure compliance with the facility’s Validation Master Plan.
- Lead Corrective Action/Preventative Action (CAPA) activities to identify and resolve root causes.
- Create and maintain validation documentation and SOPs related to risk management.
- Act as database administrator for InfinityQS software, supporting statistical process control.
- Drive root cause investigations and implement effective resolutions for validation discrepancies.
- Lead risk management projects (DFMEA, PFMEA, hazard analysis) and coordinate quality deliverables.
- Support continuous improvement initiatives that enhance compliance, profitability, and customer satisfaction.
What We’re Looking For
- Education & Experience:
- Bachelor’s degree in Engineering or related field.
- Minimum 6 years of engineering/technical experience in manufacturing, including leadership roles.
- Skills & Knowledge:
- Proficiency in quality tools and statistical methodologies (Six Sigma, FMEA, SPC, DOE).
- Strong understanding of GMPs and ISO standards in regulated industries.
- Computer proficiency (Word, Excel, Outlook, PowerPoint) and SPC software experience.
- Preferred:
- Experience in FDA-regulated environments (Medical Device, Cosmetic, OTC).
- Professional certifications (ASQ CQE/CQA/CQM, Six Sigma Green/Black Belt).
- Ability to work independently and collaboratively in a fast-paced environment.
Why Join Iatric?
- Be part of a mission-driven company that impacts health and safety across industries.
- Work in a culture that values innovation, integrity, and teamwork.
- Competitive compensation and benefits package.
- Opportunities for professional growth and development.
- Make a difference in a company where your ideas and contributions matter.
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.