Quality Control Analyst

Role overview

The Quality Control Analyst will carry out analytical testing on raw materials, in-process samples, and final pharmaceutical or biopharmaceutical products. The purpose of the role is to confirm that manufactured goods satisfy regulatory requirements, internal specifications, and Good Manufacturing Practice (GMP) expectations. This position suits someone with solid hands-on experience in wet chemistry or microbiological analysis, strong accuracy, and a strong commitment to safety and quality.

Location and working arrangement

This position is based in Dublin, Ireland. It is primarily onsite, with hybrid working options available depending on the company.

Reporting line

The role reports to the QC Supervisor or QC Manager.

Key responsibilities

• Carry out routine and non-routine testing on raw materials, intermediates, and finished products using methods such as HPLC, GC, UV-Vis, FTIR, and dissolution testing, or microbiological assays where the product area is biologics-focused.
• Document, compile, and review analytical results and laboratory records in line with cGMP, data integrity standards, and company SOPs.
• Keep laboratory equipment calibrated, maintained, and operational, and resolve basic instrumentation issues when they arise.
• Support laboratory investigations for out-of-specification and out-of-trend findings, including participation in corrective and preventive actions when needed.
• Contribute to drafting, revising, and improving SOPs and analytical test methods.
• Assist with analytical method verification, validation, and transfer activities.

Eligibility and work authorization

Candidates must already have full, unrestricted permission to work in Ireland at the time they apply. The employer is unable to offer visa sponsorship for this role. Applications that require a general employment permit or a critical skills employment permit will not be considered.

Requirements

• Bachelor’s degree or higher in Chemistry, Biochemistry, Microbiology, Pharmacy, or a closely related scientific field.
• For junior or associate-level candidates: 0 to 2 years of experience in a GMP laboratory environment, ideally within pharmaceuticals or medical devices.
• For mid-level candidates: 2 to 5 years of experience using advanced analytical equipment such as HPLC or GC.
• Working knowledge of cGMP, FDA/EMA regulatory expectations, and data integrity principles.
• Experience using laboratory systems such as Empower and LIMS.
• Strong analytical troubleshooting ability, a careful approach to detail, and structured problem-solving skills.
• Clear written and spoken communication skills, with the ability to prepare reports and work effectively with Production and QA teams.

Additional information

This is a contract role.

The job may involve wet chemistry or microbiological testing depending on the product area.

The role requires a high standard of safety, compliance, and quality at all times.

No sponsorship is available for this position.