A leading global Healthcare Manufacturer is seeking a
CAPA Specialist
to join its team in
County Cavan
. This is an excellent opportunity for a Quality Assurance professional with strong experience in
Quality Records
and
CAPA systems
. The successful candidate will 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 (or more frequent) CAPA meetings to monitor timelines, quality, and progress of Quality Records and related actions.
* Provide leadership and support to all plant personnel in the effective use of the Corrective and Preventive Action (CAPA) system.
* Monitor and report monthly metrics related to CAPAs and Quality Records.
* Ensure site Quality CAPA metrics are accurately recorded, verified, and aligned with corporate expectations.
* Deliver training to subject matter experts and broader plant teams on CAPA processes, in line with site, division, and corporate standards.
* Review site 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.
For further details please contact; Paula O'Reilly on or send CV in confidence to