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Qa analyst

Dublin
Brightwater Recruitment
Qa analyst
US$60,000 - US$80,000 a year
Posted: 21 August
Offer description

QA Analyst

Contract – Hybrid – Dublin – 4 day week

About the Company

Our client is a leading US healthcare company, with offices in Dublin city centre.

About the Position

We are seeking a Quality Assurance Analyst to support operations across Ireland and the UK. The role focuses on ensuring compliance with regulatory requirements, maintaining audit integrity, managing supplier quality, and supporting operational quality controls. This position is ideal for a quality professional with experience in regulated environments who thrives in both independent and cross-functional teamwork.

Key Responsibilities

Audit Program Support

* Plan, execute, and follow up on internal, external, and corporate audits.
* Maintain audit documentation and ensure timely closure of findings.

Supplier Quality Management

* Conduct supplier audits and evaluations.
* Maintain supplier qualification records to ensure compliance with standards and regulatory requirements.

Non-Conforming Material Oversight

* Monitor and manage non-conforming materials.
* Partner with cross-functional teams to drive timely resolution of issues.

CAPA & Change Control

* Manage Corrective and Preventive Action (CAPA) activities.
* Support and document change control processes.

Quality Documentation

* Draft, maintain, and update SOPs, procedures, and other controlled documents.

Training & Compliance

* Support quality system training activities, ensuring alignment with compliance requirements.

Operational Quality Support

* Assist with incoming inspection processes.
* Monitor environmental conditions and ensure compliance with quality standards.
* Support calibration management by scheduling, documenting, and tracking compliance of equipment.

Experience/Requirements

* Proven experience in quality assurance within medical devices, healthcare technology, or other regulated industries.
* Strong knowledge of ISO 13485:2016 and related regulatory frameworks (EU MDR, EU MDD, UK MDR).
* Certified Lead Auditor for ISO or equivalent).
* Familiarity with FDA QMSR and its alignment with ISO standards.
* Experience in supplier quality management and risk assessments.
* Strong documentation, audit, and compliance tracking skills.
* Ability to work independently and collaboratively across regions.

Key Skills

* Internal and supplier auditing (planning, execution, and follow-up).
* Supplier risk assessment and qualification management.
* CAPA management and timely closure of actions.
* Documentation control and SOP management.
* Non-conformance monitoring and resolution.
* Knowledge of environmental monitoring in regulated facilities.
* Calibration management oversight.
* Strong analytical, problem-solving, and communication skills.

Remuneration Package

A strong rate is on offer, this is a hybrid role and working a 4 day week.

Contact

Please contact Derek Smyth on or email or simply click the apply button.

To view all live jobs with Brightwater and market insights, please visit our website

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