Pharma QC Analyst: Impactful, GMP-Driven Testing

R Dpartners; Tipperary; On-site; EUR 40,000 - 60,000; Full time

Job summary

R&D Partners is seeking a qualified QC laboratory professional to support analytical testing, method validation, and transfer activities in a fast-growing pharmaceutical manufacturing environment.

The role focuses on data review, GDP, and cGMP-compliant documentation, with collaboration across manufacturing, engineering, and quality teams to ensure product quality and regulatory readiness.

Qualifications

• Experience in pharmaceutical or biotechnology QC laboratory settings.
• Knowledge of analytical instrumentation such as HPLC, GC, or analytical balances.
• Experience performing analytical testing under SOPs, cGMP, and regulatory requirements.
• Hands-on validation, verification, or transfer of methods.
• Strong GDP and good documentation practices.
• Experience supporting deviation investigations, CAPA, and root cause analysis.
• Involvement in regulatory inspections or audits.

Responsibilities

• Perform routine laboratory testing, investigations, and data review in compliance with SOPs, cGMP standards, and regulatory requirements.
• Support analytical method verification, validation, and technology transfer activities to ensure robust testing processes.
• Prepare, review, and maintain laboratory documentation, including procedures, specifications, protocols, reports, and testing records.
• Assist with laboratory operations, including equipment qualification, calibration activities, consumables management, and laboratory setup.
• Contribute to regulatory inspection readiness by supporting audits, compliance initiatives, and quality management system requirements.
• Collaborate cross-functionally with manufacturing, engineering, warehouse, and other internal teams to support operational and quality objectives.
• Promote a safe, organised, and compliant laboratory environment while ensuring all training, documentation, and quality standards are consistently maintained.

Skills

Data review

GDP

cGMP knowledge

Analytical testing

Tools

HPLC

GC

Analytical balances

Job description

R&D Partners is seeking a qualified QC laboratory professional to support analytical testing, method validation, and transfer activities in a fast-growing pharmaceutical manufacturing environment.

The role focuses on data review, GDP, and cGMP-compliant documentation, with collaboration across manufacturing, engineering, and quality teams to ensure product quality and regulatory readiness.