Quality Assurance Manager II
Iatric Manufacturing | Morristown, TN
Full-Time | Exempt | On-Site
Lead Quality. Drive Compliance. Make an Impact.
Iatric Manufacturing is seeking an experienced and strategic Quality Assurance Manager II to lead our Quality Assurance, Quality Control, and Quality Engineering teams in an FDA-regulated manufacturing environment. This role is ideal for a quality leader who is passionate about continuous improvement, regulatory compliance, product safety, and developing high-performing teams.
As a member of the site leadership team, you will partner with Operations, Engineering, Product Development, and Global Quality teams to drive quality initiatives, improve manufacturing performance, ensure regulatory compliance, and support business growth.
What You'll Do
- Lead all Quality Assurance, Quality Control, and Quality Engineering activities.
- Oversee investigations, deviations, nonconforming materials, CAPA, and quality system activities.
- Drive continuous improvement initiatives focused on quality, efficiency, and compliance.
- Ensure compliance with FDA regulations, cGMP requirements, and quality management systems.
- Lead internal and external audits and support regulatory inspections.
- Collaborate with customers, suppliers, and cross-functional teams on quality-related matters.
- Support new product introductions, process validation activities, and risk management initiatives.
- Develop, mentor, and coach quality professionals while fostering a culture of accountability and excellence.
- Lead site quality reviews, strategic planning efforts, and management review activities.
What We're Looking For
Required Qualifications
- Bachelor's degree in Science, Engineering, or a related technical discipline.
- 10+ years of Quality Assurance leadership experience within an FDA-regulated manufacturing environment.
- Experience managing Quality Assurance, Quality Control, and Quality Engineering functions.
- Strong working knowledge of:
- FDA regulations (21 CFR Parts 11, 210, 211, and 820)
- cGMP manufacturing environments
- ISO 13485
- CAPA, Root Cause Analysis, and Risk Management
- Process, Cleaning, Software, and Analytical Method Validation
- Statistical Process Control and Lean Manufacturing principles.
Preferred Qualifications
- Pharmaceutical and/or Medical Device manufacturing experience.
- Professional certifications such as Certified Quality Auditor (CQA), Certified Biomedical Auditor (CBA), Certified Pharmaceutical Professional (CPP), or Regulatory Affairs certifications.
Why Join Iatric?
At Iatric, you'll have the opportunity to influence site strategy, build high-performing teams, and help manufacture products that meet the highest standards of quality and safety. We offer a collaborative environment where continuous improvement, innovation, and professional growth are valued.
Our Values
We are committed to our RRITE Values:
- Renew
- Respect
- Integrity
- Teamwork
- Excellence
Ready to lead quality excellence? Apply today and join a team committed to delivering safe, high-quality products and continuous improvement
Equal Opportunity Employer
Iatric Manufacturing is an Equal Opportunity Employer and welcomes qualified applicants from diverse backgrounds.
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