CAPA Specialist Role
A global healthcare manufacturer seeks a CAPA specialist to lead its quality assurance team in Cavan, Ireland.
This is an excellent opportunity for professionals with strong experience in quality records and CAPA systems to provide oversight, leadership, and guidance in the initiation, investigation, and closure of quality records (QRs), driving continuous improvement across the site.
Key Responsibilities:
* Lead weekly CAPA meetings to monitor timelines, quality, and progress of quality records and related actions.
* Provide leadership and support to plant personnel in the effective use of the Corrective and Preventive Action (CAPA) system.
* Monitor and report metrics related to CAPAs and quality records on a monthly basis.
* Evaluate site quality CAPA metrics to ensure accurate recording, verification, and alignment with corporate expectations.
* Deliver training sessions on CAPA processes to subject matter experts and broader plant teams, adhering to site, divisional, and corporate standards.
* Review quality records to ensure compliance with rubric requirements, as well as site and divisional policies.
Requirements:
* Diploma or degree in science, engineering, or a related discipline (science/engineering background preferred).
* Minimum of 3 years' experience in a quality assurance role within a regulated manufacturing environment.
* Strong interpersonal and communication skills, with the ability to influence and engage across teams.
* High level of computer literacy.
* Proven ability to contribute effectively within a high-performance team environment.