Seeking a Quality Assurance Professional with experience in Quality Records and CAPA systems. This role involves providing 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 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 accurate recording, verification, and alignment of site Quality CAPA metrics with corporate expectations.
* Deliver training on CAPA processes to subject matter experts and broader plant teams in line with site, division, and corporate standards.
* Review site Quality Records to ensure compliance with rubric requirements and site policies.
Requirements:
1. Diploma or Degree in Science, Engineering, or a related discipline.
2. Minimum 3 years' experience in a Quality Assurance role within a regulated manufacturing environment.
3. Strong interpersonal and communication skills, with ability to influence and engage across teams.
4. High level of computer literacy.
5. Proven ability to contribute effectively within a high-performance team environment.
For further details please contact Paula O'Reilly at 0877094141 or send CV in confidence to paula.oreilly@lifescience.ie