QA Manager II

Iatric Manufacturing Morristown TN
Full-Time Exempt On-Site

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.

• 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.

• Bachelors 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 Partsand 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.

• 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.

At Iatric youll 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.

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.

Grade 14