QA Analyst
Overview
CLS is Ireland’s highest-accredited contract laboratory, providing industry-leading sampling, analysis, and fully trained analysts on contract across the food, environmental, medical device, biopharmaceutical, and pharmaceutical sectors.
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 analysis to 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 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.