QC Analyst I

Location: West Limerick (onsite)

Start Date: January 2026

Training: Initial onsite training in the US

Department: QC Laboratory

Reports to: QC Lab Lead

Schedule: Monday–Thursday 8:30–17:00, Friday 8:30–16:00 (39-hour week)

Role Summary

We are seeking an experienced QC Analyst I to join a collaborative QC laboratory team in West Limerick. This is a hands-on role working closely with production and reporting directly to the QC Lab Lead.

The successful candidate will begin with structured training in the US in January 2026 and will take ownership of QC testing and documentation from the outset.

This role is best suited to candidates with 2+ years of hands-on industry laboratory experience in a regulated environment.

Key Responsibilities

• Perform analytical testing using HPLC, GC, and other techniques; manage and review data using Empower.
• Carry out raw material, in-process, and finished product testing to support batch release.
• Maintain manual paper-based records, including logbooks and QC reports in compliance with SOPs.
• Support validation activities, stability studies, and environmental monitoring programs.
• Ensure GMP-compliant documentation, accuracy, and data integrity at all times.
• Maintain, calibrate, and troubleshoot laboratory instruments to minimise downtime.
• Participate in out-of-specification (OOS) investigations and CAPA activities.
• Collaborate with production teams to align QC schedules with manufacturing needs.
• Demonstrate autonomy and initiative, contributing to the efficiency and quality of QC operations.

Requirements

• Bachelor’s degree in Chemistry or related scientific discipline.
• Minimum of 2 years’ hands-on QC or analytical laboratory experience in industry (pharma, biopharma, or regulated manufacturing).
• Technical competence in HPLC and GC; Empower experience preferred.
• Strong documentation skills, including manual logbook and report writing.
• Knowledge of USP/EP testing and FDA/ISO requirements.
• Ability to work independently and within a small, collaborative team.
• Excellent communication and interpersonal skills.

What’s on Offer

• Start date January 2026, with structured training in the US.
• Day-based role, Monday–Friday (39 hours/week).
• A technically varied QC position with exposure to analytical testing, validation, and production support.
• Supportive, collaborative, and hands-on team culture.
• Competitive salary and benefits package.

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