Quality Manager

Cardinal Health•Deland, FL

13d

About The Position

What Quality Management contributes to Cardinal Health Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Management provides strategic oversight, leadership and direction within the Quality function.

Requirements

Minimum 3 years of experience in a quality manager or quality engineer role for a medical device manufacturing company required
Minimum 4 years of leadership experience in managing both hourly and salary professionals required.
Experience with root cause analysis, corrective actions and documentation control required.
Bachelor’s degree in related field, or equivalent work experience, preferred
Manages department operations and supervises professional employees, front line supervisors and/or business support staff
Participates in the development of policies and procedures to achieve specific goals
Ensures employees operate within guidelines
Decisions have a short term impact on work processes, outcomes and customers
Interacts with subordinates, peers, customers, and suppliers at various management levels; may interact with senior management
Interactions normally involve resolution of issues related to operations and/or projects
Gains consensus from various parties involved

Responsibilities

Develop and implement quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications.
Provide strategic oversight, leadership and direction to direct reports within the Quality function.
Manage, develop, train and guide direct reports, quality staff, and site personnel to achieve site quality goals and maintain regulatory compliance.
Lead audit readiness efforts and facilitate regulatory, customer and corporate audits such as (FDA and MDSAP) and customer technical visits and provide responses to findings in a timely manner.
Conducting Site Quality Management Reviews and report KPI metrics to corporate.
Responsible for identifying trends and making decisions that affect product release to ensure patient safety.
Responsible for understanding ISO 13485, FDA QSR and other relevant standards and to apply them to continuous improvement of the Quality Management System.
Manage internal audits, external audits, and regulatory inspections.
Oversee document control, CAPA (Corrective and Preventive Actions), NCR (Non-Conformance Reports), and complaint handling in a manufacturing environment.
Support risk management activities, including hazard analysis and FMEA.
Ensure quality oversight throughout product lifecycle — from design control and supplier qualification to manufacturing and post-market surveillance.
Collaborate with engineering, production, and supply chain teams to ensure product quality and process compliance.
Train and mentor staff on quality procedures and regulatory requirements.
Lead root cause analysis and problem-solving initiatives for quality issues.
Analyze quality metrics and identify trends for escalation to senior management as required.