Quality Manager
Date Posted: 3/24/2026
Job Snapshot
- Employee Type:
- Permanent
- Location:
- Walton, KY
- Job Type:
- Logistics & Warehouse
- Date Posted:
- 3/24/2026
Job Description
Job Summary:
The Quality Manager supports the Quality Management System and will perform tasks to ensure the quality department meets QA requirements and Regulatory compliance while directly supporting the Director of Quality. This role will be maintaining a compliant Quality System, will be responsible for reporting compliance issues directly to the Director of Quality, must have quality experience and will be expected to perform all tasks in a safe manner observing cGMP and quality standards.
Responsibilities:
- Maintains Non-Conformance System & Investigations, including contacting appropriate people to resolve and providing guidance and strategies to various groups within the organization.
- Frequently interacts and partners with Operations, Purchasing and other departments to develop and administer all aspects of current and expanding quality processes for a successful cross-functional team.
Exercises judgement within defined practices and policies in critical thinking and problem solving. - Manage a team of QA/QC staff to ensure all members are competently performing their duties and are trained in all quality requirements.
- Lead process improvement and problem-solving efforts with other departments
Assists with internal audits. - Liaison with 3 rd Party Testing Laboratories
- Responsible for Quality Review of Batch Record for release of product.
- Maintains Document and Data/ Records Control.
- Maintains all Quality System Records.
- Reviews and approves other documents: QC sheets, Lab documents, Certificates of Analysis.
- Issues and maintains NCR, COR, and Deviation system.
- Reviews and approves other documents: QC sheets, Lab documents, Certificates of Analysis, Cleaning/Sanitizing. Seeks answers and information regarding customer or in-house problems with product quality or performance.
Exercises judgement within defined practices and policies in critical thinking and problem solving.
Assists with internal audits.
Seeks answers and information regarding customer or in-house problems with product quality or performance.Qualifications:
- Bachelor's degree in science, engineering, or technical field.
- Minimum 3 years' experience in FDA regulated environment.
Minimum 3 years' experience working in a Quality Department. - Must have cGMP Experience.
- Ability to perform systems, process, and product audits.
- Ability to work efficiently in a fast-paced, high-volume environment.
- Strong attention to detail and strong sense of urgency.
- Well organized with excellent communication skills, leadership, and interpersonal skills Ability to maintain confidentiality.
- Strong analytical and effective problem-solving skills.
- ASQ Certifications.
- Ability to work well as part of the Quality team.
- Computer skills, including Microsoft Office.
- Ability to manage multiple projects and meet deadlines.
Minimum 3 years' experience working in a Quality Department.
Ability to maintain confidentiality.