Sr. Specialist, QA

What Quality Assurance 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 Assurance develops and implements a compliant and cost-effective quality system that assures products and services are reliable, safe and effective. This job family provides oversight of production/manufacturing activities, training to operational and quality control personnel, and educates business leaders on Quality policies and procedures and ensures that all products and services are properly reviewed for quality and documented.

The Senior Specialist supports Regulatory Operations and advances global regulatory compliance through the management of regulatory processes, systems, data, and operational activities across the product lifecycle. This role serves as a key contributor to regulatory operations by ensuring the accuracy, integrity, and compliance of regulatory information used for global submissions, registrations, product maintenance, and post-market activities. The Senior Regulatory Affairs Specialist applies a strong understanding of medical device or pharmaceutical regulations, Quality Management system and regulatory operations processes to maintain compliant regulatory databases, support global market registrations, facilitate regulatory reporting, and drive process improvements. Working collaboratively with Regulatory Affairs, Quality, R&D, Clinical, Manufacturing, Supply Chain, and IT, this individual contributes to the development of scalable and efficient regulatory operations capabilities that support business objectives and regulatory compliance.

Regulatory Operations & Compliance Support the development, implementation, and continuous improvement of regulatory operations processes, procedures, systems, and tools. Ensure compliance with applicable global regulatory requirements, including FDA regulations, EU MDR, ISO 13485, and other international regulatory frameworks. Monitor changes in regulatory requirements and assess potential impacts on regulatory operations processes and systems. Regulatory Data Management - Maintain, review, and manage regulatory data within internal systems and regulatory databases. Conduct technical review, remediation, and verification of regulatory data to ensure completeness, accuracy, consistency, traceability, and compliance. Support regulatory submissions and registrations through data preparation and maintenance activities, including databases such as GUDID, EUDAMED, and other global regulatory systems. Systems, Reporting & Analytics Support administration, enhancement, and effective utilization of regulatory information management systems and other digital tools supporting regulatory compliance. Develop and maintain reports, dashboards, and performance metrics utilizing tools such as Excel, Power BI, and similar reporting platforms. Analyze regulatory data to identify trends, compliance risks, and opportunities for process improvements. Partner with business stakeholders and IT teams to support system improvements, data migrations, and implementation of new technologies. Quality & Audit Readiness Support internal and external audits, inspections, and compliance assessments by preparing documentation and providing evidence of regulatory compliance. Assist in risk assessments related to regulatory processes, systems, and data integrity. Maintain inspection readiness by ensuring regulatory records and documentation are complete, accurate, and retrievable. Project & Cross-Functional Support Independently manage low to medium medium-complexity projects and assigned regulatory operational initiatives. Collaborate with cross-functional teams to resolve operational challenges and improve regulatory processes. Support regulatory labeling, Instructions for Use (IFUs), Declarations of Conformity (DoCs), website postings, and other