QC Analyst

3 days ago

Limerick, Ireland Cpl Full time

QC Analyst I – Pharmaceutical / Life Sciences Sector

Location: Ireland

Job Type: Full-Time, Monday–Friday (shift work, flexibility required)

Level: Entry to Junior (1–2+ years’ experience)

Reports to: QC Laboratory Lead

About the Role

We are seeking a QC Analyst I to join a growing Quality Control Laboratory team. This role involves routine analytical testing of raw materials, in-process samples, and finished products, supporting both production and wider laboratory operations. It offers strong exposure to GMP environments and the opportunity to build technical expertise across a range of analytical techniques.

Key Responsibilities

Carry out analytical testing using HPLC, GC, FTIR, UV-VIS and other instrumentationSample and test raw materials to support timely release into productionAccurately record, review, and report results in line with GMP, SOPs, and regulatory standardsMaintain laboratory notebooks, reports, and electronic documentationAssist with out-of-specification investigations and data integrity complianceSupport audit readiness and compliance with FDA, ISO, and cGMP requirementsTroubleshoot and maintain QC laboratory equipment to minimise downtimeEnsure laboratory activities are delivered on schedule to meet production timelinesContribute to environmental monitoring, stability studies, and validation projectsMaintain a clean, safe, and organised laboratory environment (5S practices)Follow all SOPs, safety procedures, and Good Laboratory Practice (GLP)

What We’re Looking For

Bachelor’s degree in Chemistry or a related scientific discipline (minimum requirement)1–2+ years’ experience in a QC or analytical laboratory environmentBackground in FDA or ISO-regulated environments (preferred)Familiarity with Empower software (advantageous)Strong communication skills – written and verbalProficiency with Microsoft Word, Excel, and AccessStrong attention to detail, problem-solving skills, and ability to work to deadlines

What’s on Offer

Full-time, permanent role with structured training and development opportunitiesExposure to a regulated pharmaceutical / life sciences environmentHands-on experience with industry-standard instrumentation (HPLC, GC, FTIR, UV-VIS)Opportunity to gain experience with stability, validation, and regulatory compliance projectsCollaborative team environment with clear career progression pathways

This role is well-suited for an early-career QC professional with a strong chemistry background and some laboratory experience who is eager to develop further within a GMP-regulated environment.

#LI-DB4

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