Quality Coordinator

Force; Mullingar; On-site; EUR 35,000 - 52,000; Full time

Benefits offered by this job

Career development

Quality systems exposure

Modern working environment

Healthcare impact

Job summary

Force, Mullingar, Ireland, is seeking a Quality Coordinator (QC) to join a regulated manufacturing environment serving healthcare, medical technology and life sciences sectors. You will monitor quality of incoming, in-process and finished goods, support QA systems, inspections, audits and CAPA, and collaborate with Production, Engineering and Quality teams to maintain high product quality.

This is a permanent role with 4-cycle shift pattern (days and nights).

Qualifications

• A third-level qualification in Quality or a related discipline, or relevant experience in a similar role.
• Strong analytical skills with the ability to interpret data and prepare reports.
• Excellent written and verbal communication skills.
• Good organisational skills and the ability to manage multiple priorities effectively.

Responsibilities

• Perform inspections (incoming, in-process, final) to ensure quality requirements are met.
• Support quality systems activities, document control and compliance with ISO standards.
• Participate in investigations, CAPA, non-conformance and continuous improvement initiatives.
• Collaborate with Production, Engineering and Quality teams to maintain product quality and standards.

Skills

Analytical skills

Communication skills

Organisational skills

Education

Third-level qualification in Quality

Job description

Quality Coordinator (QC)

Location: Mullingar, Co. Westmeath
Job Title: Quality Coordinator (QC)
Role Type: Permanent, 4-cycle shift pattern (days and nights, with every second weekend rostered on)

Job Description

An opportunity is available for a Quality Coordinator to join a quality team within a regulated manufacturing environment supporting the healthcare, medical technology and life sciences sectors.

The role offers the opportunity to develop experience in quality assurance, compliance and continuous improvement while contributing to the manufacture of high-quality products.

About the Role

The Quality Coordinator is responsible for monitoring the quality of incoming, in-process and outgoing products to ensure compliance with customer, regulatory and internal quality requirements. The role supports quality systems, inspections, audits and process improvements to maintain high standards of product quality.

Key Responsibilities

• Perform incoming, in-process and final inspections to ensure products meet established quality requirements.
• Support quality systems activities, including batch record generation, document control and compliance with relevant ISO standards.
• Participate in investigations, Corrective and Preventive Actions (CAPA), non-conformance activities and continuous improvement initiatives.
• Collaborate with Production, Engineering and Quality teams to support product quality and operational standards.

The Ideal Candidate Will Have

• A third-level qualification in Quality or a related discipline, or relevant experience in a similar role.
• 1–2 years’ experience in a regulated manufacturing environment.
• Excellent written and verbal communication skills.
• Strong analytical skills, with the ability to interpret data and prepare reports.
• Good organisational skills and the ability to manage multiple priorities effectively.

What’s on Offer

• An opportunity to develop a career within the medical technology and life sciences sectors.
• Exposure to quality systems, audits, regulatory compliance and continuous improvement initiatives.
• A modern working environment that promotes safety, quality, teamwork and professional development.
• The opportunity to contribute to the manufacture of products that support healthcare and improve lives.