Quality Systems Associate

LGC; Ballina; On-site; EUR 30,000 - 40,000; Full time

Job summary

A leading clinical diagnostics company in Ballina is seeking a motivated Quality Systems Associate to support various quality systems activities. This role offers a fantastic opportunity for someone early in their career, providing exposure to quality management systems and regulatory standards. The company promotes ongoing career development and a supportive culture driven by core values.

Benefits

25 days annual leave

Health allowance and life assurance

Retail discounts

24/7 Employee Assistance Programme

Recognition & reward schemes

Ongoing career development opportunities

Qualifications

• 1-2 years’ experience in QA / regulated manufacturing.
• Curiosity to learn regulatory standards: FDA 21 CFR 820, ISO 13485.
• Familiarity with ISO 14971 (Risk Management).

Responsibilities

• Support the implementation and maintenance of the Quality Management System.
• Assist in supplier quality activities and performance monitoring.
• Contribute to internal audits and support external inspections.

Skills

Attention to detail

Organisational skills

Willingness to learn

Positive attitude

Education

Degree in Science, Engineering, or related field

Tools

ISO standards

Job description

Company Description

LGC is a world-class Clinical Diagnostics company committed to improving patient healthcare. We are looking for a motivated and ambitious Quality Systems Associate to join our growing QA team in Ballina. This is a fantastic opportunity for someone early in their quality career who wants to develop into a future QA Specialist.

Job Description

You’ll support a broad range of quality systems activities, including:

• Support the implementation and maintenance of our Quality Management System (QMS)
• Assist in supplier quality activities, including performance monitoring and non-conformance investigations
• Contribute to internal audits and support external inspections (HPRA, Notified Body, Customers)
• Help review and maintain documentation (SOPs, records, manufacturing documents)
• Gain exposure to CAPA, Change Control, and Document Control processes
• Maintaining strong housekeeping and compliance with Health & Safety policies

Qualifications

• A degree in Science, Engineering, or a related field
• 1-2 years’ experience in QA / regulated manufacturing
• Strong attention to detail, organisation, and willingness to learn
• A positive attitude and the drive to build a career in Quality
• Understanding of / curiosity to learn regulatory standards: FDA 21 CFR 820, ISO 13485, IVDD 98/79/EC, IVDR (EU) 2017/746
• Familiarity with ISO 14971 (Risk Management)

What’s in it for you?

• 25 days annual leave
• Health allowance and life assurance
• Retail discounts (local and national)
• 24/7 Employee Assistance Programme
• Recognition & reward schemes
• Ongoing career development & progression opportunities
• A supportive culture driven by our values: Passion, curiosity, integrity, brilliance and respect