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
1. Carry out analytical testing using HPLC, GC, FTIR, UV-VIS and other instrumentation
2. Sample and test raw materials to support timely release into production
3. Accurately record, review, and report results in line with GMP, SOPs, and regulatory standards
4. Maintain laboratory notebooks, reports, and electronic documentation
5. Assist with out-of-specification investigations and data integrity compliance
6. Support audit readiness and compliance with FDA, ISO, and cGMP requirements
7. Troubleshoot and maintain QC laboratory equipment to minimise downtime
8. Ensure laboratory activities are delivered on schedule to meet production timelines
9. Contribute to environmental monitoring, stability studies, and validation projects
10. Maintain a clean, safe, and organised laboratory environment (5S practices)
11. Follow all SOPs, safety procedures, and Good Laboratory Practice (GLP)
What We're Looking For
12. Bachelor's degree in Chemistry or a related scientific discipline (minimum requirement)
13. 1–2+ years' experience in a QC or analytical laboratory environment
14. Background in FDA or ISO-regulated environments (preferred)
15. Familiarity with Empower software (advantageous)
16. Strong communication skills – written and verbal
17. Proficiency with Microsoft Word, Excel, and Access
18. Strong attention to detail, problem-solving skills, and ability to work to deadlines
What's on Offer
19. Full-time, permanent role with structured training and development opportunities
20. Exposure to a regulated pharmaceutical / life sciences environment
21. Hands-on experience with industry-standard instrumentation (HPLC, GC, FTIR, UV-VIS)
22. Opportunity to gain experience with stability, validation, and regulatory compliance projects
23. 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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