QA Analyst

CLS - Complete Laboratory Solutions; Galway; On-site; EUR 30,000 - 40,000; Full time

Job summary

CLS - Complete Laboratory Solutions is seeking a QA/QC professional to monitor and improve quality across client projects in Ireland. The role involves data analysis, audits, and collaboration with cross-functional teams to ensure GMP/GDP compliance.

You will review documentation, support deviations, and contribute to continuous improvement while upholding stringent safety and quality standards in accredited labs and client sites.

Qualifications

• Experience in QA/QC within pharmaceutical, medical device or biotech industries.
• Understanding of GMP/GDP principles and regulatory requirements.
• Ability to review data, write deviations/investigations, and perform audits.

Responsibilities

• Monitor and evaluate processes to ensure quality standards.
• Analyse data, conduct audits and drive improvements.
• Collaborate with cross-functional teams to ensure regulatory compliance.
• Prepare comprehensive QA reports and maintain documentation.
• Support change controls and risk assessments.
• Contribute to training and continuous improvement initiatives.

Skills

QA/QC knowledge

GMP/GDP experience

Data analysis

Audit skills

Education

Bachelor's in Chemistry/Biology/Pharma

Tools

LIMS

Regulatory databases

Job description

Overview

CLS is currently going through an unprecedented and exciting period of growth and development and is looking for dedicated, solutions driven team members with a flexible approach, who want to be part of the company’s continued success.

Founded in 1994, Complete Laboratory Solutions (CLS) is the highest accredited contract laboratory in Ireland, providing industry-leading sampling and analysis; and fully trained micro and analytical analysts on contract to clients in the food, environmental, medical device, biopharmaceutical, and pharmaceutical sectors.

We offer bespoke managed service solutions that give clients the option of having our expert team on-site at their own facility or outsourcing those services to us here at CLS.

What’s Important

• Structured QA Program, learning methods and skills such as auditing, investigation, review, risk management, aseptic processing etc.
• Building a strong foundation in GMP-regulated environments.
• Developing applied scientific knowledge through CLS’ proprietary training programmes.
• Growing technical, professional, and leadership skills.
• Progressing into a specialised career pathway within CLS or client organisations.

The Role

Duties and responsibilities may vary between clients but generally, the role will involve monitoring and evaluating operational processes and outputs to ensure they meet established quality standards, and analysing data, conducting audits and working closely with various teams to drive improvements and ensure customer satisfaction.

• Receive training on QA Modules and develop skills such as investigation, auditing, risk management, review of documentation, regulatory compliance etc.
• Use LIMS for data management and reporting.
• Ensure compliance with GMP, GDP, and all other standards.
• Collaborate effectively within a team while also working independently.
• Conduct detailed analysisto identify trends, issues, and areas for improvement in product and process quality.
• Perform regular quality assurance audits to ensure adherence to established standards and regulatory compliance.
• Develop and maintain quality standards and procedures in collaboration with cross-functional teams.
• Analyse test results and produce comprehensive reports detailing findings and recommending actionable improvements.
• Create and maintain detailed documentation for quality testing and assurance activities.
• Foster a culture of continuous improvement, identifying inefficiencies and suggesting enhancements to products and processes.
• All other reasonable duties as assigned by your manager.

Quality Assurance:

• Internal and external Auditing skills
• Investigation and Technical writing skills for Deviations and Investigations
• Review of data sets
• Change control procedures and documentation updates
• Develop risk-based approach to tasks

Where You Come From

• A third level qualification in a related Science discipline.
• 1+ years experience in a related QA/QC role.
• Basic knowledge of regulatory bodies and compliance to regulations.
• Who You Are
• Passionate about pursuing a career in the pharmaceutical or medical device industry
• Motivated, adaptable, and eager to learn.
• Excellent attention to detail, strong organisational skills and the ability to prioritise workload in a fast-paced environment.
• Demonstrated ability to juggle multiple tasks with competing deadlines, agility to prioritise most critical tasks.
• Good written and verbal communication skills with the ability to prepare clear reports and interact professionally with colleagues and clients.
• Commitment to maintaining confidentiality, data integrity and high standards of safety and quality.
• Demonstrate strong critical thinking skills and adaptability in fast-paced, changing environments, with the ability to assess risk, evaluate options, and make informed decisions while maintaining quality and compliance standards.

What We Offer

• A full-time, permanent role from day one.
• Hands-on experience in accredited labs and client sites.
• Opportunities for professional growth in a dynamic, expanding industry.
• A collaborative and supportive working environment.