QC Analyst

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 instrumentation
• Sample and test raw materials to support timely release into production
• Accurately record, review, and report results in line with GMP, SOPs, and regulatory standards
• Maintain laboratory notebooks, reports, and electronic documentation
• Assist with out-of-specification investigations and data integrity compliance
• Support audit readiness and compliance with FDA, ISO, and cGMP requirements
• Troubleshoot and maintain QC laboratory equipment to minimise downtime
• Ensure laboratory activities are delivered on schedule to meet production timelines
• Contribute to environmental monitoring, stability studies, and validation projects
• Maintain 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 environment
• Background in FDA or ISO-regulated environments (preferred)
• Familiarity with Empower software (advantageous)
• Strong communication skills – written and verbal
• Proficiency with Microsoft Word, Excel, and Access
• Strong 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 opportunities
• Exposure to a regulated pharmaceutical / life sciences environment
• Hands-on experience with industry-standard instrumentation (HPLC, GC, FTIR, UV-VIS)
• Opportunity to gain experience with stability, validation, and regulatory compliance projects
• Collaborative 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.

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