QC Analyst I – Pharmaceutical / Life Sciences Sector (Ireland)
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.
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)
Qualifications
* 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.
Note: This description reflects the core responsibilities and requirements for the QC Analyst I role and does not include unrelated postings or extraneous content.
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