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Paula O'Reilly
Life Science

+353 1 507 9265
[email protected]
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Details

CAPA Specialist


Reference:POR/586666 Location: Cavan
Qualification:DegreeExperience:3-4 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: Quality Specialist

A leading global Healthcare Manufacturer is seeking a CAPA Specialist to join its team in 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 00 353 (0)87 7094141 or send CV in confidence to [email protected]