Find pharmaceutical external Jobs in dublin, d

Quality Complaint & Recall Administrator
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DPS Group —Dublin, County Dublin
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Novartis —Dublin, County Dublin
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Regional Lead Aseptic Excellence (Pharma)
MSD —Leopardstown, County Dublin
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Takeda Pharmaceutical —Dublin, County Dublin
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Alexion Pharmaceuticals,Inc. —Dublin, County Dublin
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EVERSANA —Dublin, County Dublin
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Senior Specialist Regulatory Key Initiatives
Viatris —Northern Cross, County Dublin
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Quality Complaint & Recall Administrator

Exertis -
Leopardstown, County Dublin

Apply Now

Job details

Permanent
5 days ago

Qualifications

ISO 9001
Organisational skills
Quality systems
Communication skills

Full job description

Req ID: 9320

Company: Vital Healthcare - Fannin Ltd

Salary: salary not disclosed

Location: Leopardstown, IE, Dublin 18

Belfast, IE, BT3 9LN

Kilcoole, IE

Contract Type: Permanent

Date Posted: 2 Jun 2026

Quality Complaint & Recall Administrator
TECHNICAL DIVISION

Job title: Quality Complaint and Recall Administrator
Location: Fannin House, Leopardstown, D18
Reporting to: Quality & Regulatory Lead Medical Devices

Summary
The Quality Complaints & Recall Administrator is responsible for the coordination and administration of complaint handling, product recalls and Field Safety Corrective Actions (FSCAs) within a regulated pharmaceutical and medical device distribution environment. The role supports compliance with GDP, GMP, MDR and IVDR requirements through effective investigation, documentation, reporting and follow-up of quality activities, while supporting Quality Management System processes and maintaining audit readiness.

Principal Duties and Responsibilities:

Administration and coordination of the end-to-end complaint handling process
Coordination of product recalls and Field Safety Corrective Actions (FSCAs)
Ensure compliance with:

o GDP, GMP, MDR and IVDR requirements
o Vigilance and regulatory reporting requirements
o Ensure complaints are assigned, investigated, and closed within defined timelines.
o Escalate critical or potentially serious quality issues to the RP/QP/PRRC/Manager as appropriate.

Maintain inspection and audit readiness through accurate documentation and record management
Perform:

o Complaint trending and data analysis
o KPI monitoring and reporting
o Training coordination for personnel on relevant quality processes

Liaise with:

o Customers
o Suppliers and manufacturers
o Regulatory authorities
o Internal stakeholders across all departments

Quality Management System Responsibilities

Administration of Quality Management System (QMS) processes related to complaints, FSCAs and recalls
Support quality processes including:

o Change Control
o Non-Conformance and CAPA management
o Internal and external audits
o Risk assessment and risk management activities

SOP authoring, review and document control administration
Completion of customer quality questionnaires and requests
Support regulatory activities including liaison with the Health Products Regulatory Authority and Medicines and Healthcare products Regulatory Agency
Support quality and compliance-related projects
Preparation and submission of monthly, quarterly and annual KPI reports
Provide cross-functional support and cover for other team members as required
Carry out additional duties appropriate to the role as assigned

Desirable Qualifications & Experience

Relevant third-level qualification in Science, Quality, Regulatory Affairs or a related discipline
Knowledge of pharmaceutical and medical device terminology
Working knowledge of ISO 9001 quality systems
Experience working within GDP and/or GMP regulated environments
Experience using QMS software systems
Full Irish driving licence and access to transport desirable

Desired Characteristics

Proactive with strong organisational skills
Flexible and adaptable in a fast-paced regulated environment
Strong problem-solving and troubleshooting capability
Excellent written and verbal communication skills
Strong interpersonal skills with the ability to communicate effectively at all levels internally and externally
Ability to work independently while managing multiple priorities
High attention to detail and commitment to quality and compliance

- FANNIN IS AN EQUAL OPPORTUNITY EMPLOYER -

Although the above is a description of the requirements of your job, as stated in your contract of employment, you may be required to carry out other reasonable duties as the Company may require from time to time.

Apply Now

Refine Your Search

pharmaceutical external jobs in dublin, d

Quality Complaint & Recall Administrator

Director, Medical Society Partnerships & Congresses

NPI Process Engineer

HR Administrator

Capital Sales Specialist - Life Science, Ireland

Director, Government Affairs Europe

CMC Lead, Launch Product, Small Molecules

Project Manager – Process Equipment

Director Regulatory Affairs Global CMC

Associate Director, Pharmacology

Corporate Development Associate

Risk Surveillance Lead

Support Pharmacist

Global Supply Planner

Maintenance & Calibration Lead

Regional Lead Aseptic Excellence (Pharma)

Senior Treasury Analyst

Senior Manager - Network Supply Planning

Associate, Contract Management

Senior Specialist Regulatory Key Initiatives

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