Excellent opportunity for a QA Compliance Engineer to join a Medical Devices Leader in the North West of Ireland. The QA Compliance Engineer will support 24/7 manufacturing teams by ensuring adherence to Good Manufacturing Practices (GMP), preparing for audits, providing training, and ensuring procedural compliance. Additionally, you are accountable for complying with relevant Corporate and Divisional Policies.
Overview of your responsibilities (full job description available on request)
Ensure compliance with Corporate and Divisional Policies and perform assigned duties.
Assess the Operations department for safe, compliant product delivery.
Support Ops Manufacturing in GMP and Audit Readiness.
Ensure adherence to site procedures, contributing to their design and update.
Promptly address any risk areas affecting product or safety.
Identify opportunities for improvements in manufacturing and Quality systems.
Manage multiple responsibilities while adhering to project plans and timelines.
Handle CAPA, completing impact assessments and investigations for non-conformances, OOS, audit findings, and customer complaints.
Knowledge, Skills and Experience Required for the Role:
Science, Engineering, or Manufacturing qualification.
Preferably three years of relevant QA Compliance experience.
Self-motivated with significant project experience and the ability to influence others.
Strong communication and interpersonal skills.
For a confidential discussion and more information on the role contact Courtney Russell
+353 (0) 71 9108062