QA Review Specialist – Pharma GMP & Compliance

CLS - Complete Laboratory Solutions; Limerick; On-site; EUR 52,000 - 65,000; Full time

Job summary

CLS is seeking a QA Reviewer to support Quality Assurance activities within a pharmaceutical manufacturing environment. The successful candidate will review analytical and batch documentation to support timely and compliant product releases.

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

Qualifications

• Degree in Chemistry, Pharmaceutical Science or related discipline (min Level 7).
• Ideally 2 years' GMP lab or pharma manufacturing experience.
• Experience reviewing analytical data and GMP documentation.
• Strong GMP and Data Integrity knowledge.
• Experience with batch record review and product release.
• Familiarity with HPLC, GC, KF, IR, PSD, X-Ray and wet chemistry.
• Experience using LIMS or TrackWise systems.

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.
• 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.

Skills

Detail-oriented

QA mindset

Communication

Organised

Problem solving

Team collaboration

Education

Bachelor's degree in Chemistry or Pharmaceutical Science

Tools

LIMS

TrackWise

Job description

CLS is seeking a QA Reviewer to support Quality Assurance activities within a pharmaceutical manufacturing environment. The successful candidate will review analytical and batch documentation to support timely and compliant product releases.

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