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.

The Role

We are currently seeking a QA Reviewer to support Quality Assurance activities within a pharmaceutical manufacturing environment. The successful candidate will be responsible for reviewing analytical and batch documentation to support the timely and compliant release of products. Working closely with QA, QC and Manufacturing teams, you will ensure analytical results and documentation meet GMP, quality and regulatory requirements. This role offers an excellent opportunity to join a growing quality team and contribute directly to product quality, compliance and patient safety.

Key Responsibilities

Review HPLC analytical data, laboratory records and GMP documentation.
Review batch documentation to support product release activities.
Ensure documentation and analytical results meet quality and regulatory requirements.
Support documentation approval and QA review processes.
Assist with investigations, deviations and quality-related activities as required.
Identify discrepancies, errors and potential compliance issues.
Collaborate with QA, QC and Manufacturing teams to ensure efficient product release.
Maintain compliance with GMP and Data Integrity requirements.
Promote high standards of quality, safety and operational excellence.

Who You Are

Detail-oriented with excellent documentation review skills.
Passionate about quality, compliance and continuous improvement.
Able to identify issues and implement effective solutions.
A strong communicator capable of working across multiple departments.
Organised, proactive and capable of managing competing priorities.
Flexible and adaptable within a fast-paced pharmaceutical environment.
A collaborative team player committed to maintaining high quality standards.

Where You Come From

Degree in Chemistry, Pharmaceutical Science or a related scientific discipline (minimum Level 7).
Ideally 2 years' experience within a GMP laboratory, Quality or pharmaceutical manufacturing environment.
Experience reviewing analytical data and GMP documentation, ideally including HPLC data.
Strong understanding of GMP requirements and Data Integrity principles.
Experience supporting batch record review and product release activities.
Knowledge of analytical techniques such as HPLC, GC, KF, IR, PSD, X-Ray and wet chemistry would be advantageous.
Experience using LIMS, TrackWise or similar laboratory and quality management systems.
Excellent attention to detail and the ability to identify documentation and compliance issues.
Strong organisational, communication and stakeholder management skills.

What We Offer

Opportunity to join a growing and dynamic pharmaceutical organisation.
A collaborative and supportive team environment.
Exposure to Quality Assurance, Quality Control and Manufacturing operations.
Professional development and career progression opportunities.
The opportunity to play a key role in ensuring the quality, safety and compliance of pharmaceutical products.

QC Analyst

Benefits

Job Description