QC Analyst

Cpl; Killaloe Municipal District(2014-2019); On-site; EUR 35,000 - 45,000; Full time

Job summary

A leading healthcare recruitment agency is seeking a QC Analyst to join a collaborative QC laboratory team in Killaloe, Co. Clare. This hands-on role involves developing testing proficiency across clinical laboratory instruments and performing QC release analysis. Candidates should have at least 1 year of experience in a regulated laboratory environment and a BSc in a relevant science discipline. Strong teamwork, attention to detail, and problem-solving skills are essential. Own transport is necessary due to location.

Qualifications

• 1+ years of hands-on industry laboratory experience in a regulated environment.
• Knowledge of GLP and GDP requirements.
• Excellent attention to detail and problem-solving skills.

Responsibilities

• Perform analysis using various clinical laboratory instruments.
• Complete routine maintenance on laboratory equipment.
• Perform QC release analysis for products.

Skills

Hands-on industry laboratory experience

Teamwork

Attention to detail

Problem solving

Ability to multitask

Education

BSc qualification in a relevant Science discipline

Tools

Microsoft Office

Job description

We are seeking a QC Analyst to join a collaborative QC laboratory team in Killaloe Co. Clare. This is a hands-on role working closely with production and reporting directly to the QC Lab Lead.

To perform this job successfully, an individual must be able to capably perform each of the following essential functions: develop testing proficiency across various clinical laboratory instruments and become competent in completing QC release analysis, value assignment, and any other required testing to exemplary GLP (Good Laboratory Practice) standards. Teamwork, ability to multitask, problem solving and attention to detail are key skills for this role.

This role is best suited to candidates with 1+ years of hands-on industry laboratory experience in a regulated environment.

Key Responsibilities

• Become proficient in performing analysis using various clinical laboratory instruments.
• Complete routine maintenance and troubleshoot issues on all laboratory equipment.
• Perform value assignment and target value testing for products.
• Perform QC release analysis for products including stability testing, bioburden analysis, physical appearance inspections.
• Assist in technical investigations and other testing requests as required.
• Work with the QC team to analyse, collate and document QC generated data within specified timelines.
• Ensure exemplary GLP and GDP standards are maintained.
• Responsibility to manage QC inventory, including stock monitoring, preparation of material orders and other tasks as assigned.
• Identify and communicate areas for continuous improvement.
• Performs other related duties as assigned by QC Manager.

Skills / Experience

• BSc qualification in a relevant Science discipline is preferable.
• Minimum 2 years’ experience in a clinical laboratory or other regulated medical product environment.
• Proficiency on Microsoft office is required.
• Knowledge of GLP and GDP requirements.
• Excellent attention to detail, problem solving skills and ability to prioritize workload.
• Positive attitude, flexibility, and ability to work in a team driven environment.

Candidates must have their own transport as there is no public transport in this location.

[e-mail]061208649or0879077699

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