QC Chemistry

Y-Axis; Dublin; Ibrido; EUR 42.000 - 64.000; Tempo pieno

Descrizione del lavoro

R&D Partners in Ireland seeks a QC laboratory professional to perform routine analytical testing and data review in a cGMP environment. You will collaborate with cross-functional teams to ensure compliant laboratory operations.

You will support method validation/verification, tech transfer, and robust documentation while contributing to audits and CAPA processes. A pharma/biotech QC background is essential.

Competenze

• Pharmaceutical/biotech QC lab experience required.
• Good Documentation Practice (GDP) knowledge essential.
• Experience with deviation investigations, CAPA and root cause analysis preferred.
• Experience supporting regulatory inspections and audits desired.

Mansioni

• Perform routine laboratory testing, investigations and data review in line with SOPs and regulatory requirements (cGMP).
• Support method verification, validation and technology transfer activities.
• Prepare, review and maintain laboratory documentation (procedures, protocols, reports).
• Assist with instrument qualification, calibration, consumables management, and lab setup.

Conoscenze

Attention to detail

Data analysis

Documentation

Team collaboration

Formazione

Bachelor's degree in Pharmaceutical Science or related field

Strumenti

HPLC

GC

Analytical balances

cGMP compliance

Descrizione del lavoro

About the job

R&D Partners is working alongside a rapidly growing, internationally recognised pharmaceutical manufacturer with a strong and expanding presence in Ireland. Operating from a state-of-the-art facility, the organisation specialises in the development and production of complex, high-value medicines, including inhalation products and other specialty therapies.

As part of a wider global network, the site plays a strategic role in supporting ongoing international growth and market expansion, with continued investment in both manufacturing and research capabilities. The facility is currently transitioning into a fully commercial operation, marking a significant phase of growth, innovation, and long-term development, with plans to scale operations and increase headcount as part of its future vision.

Please note that to be considered for this role you must have the right to work in Ireland.

• Job Duties: 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.
• Background Requirements: Pharmaceutical or biotechnology QC laboratory
• Knowledge of analytical instrumentation (e.g., HPLC, GC, analytical balances, or equivalent platforms)
• Proven experience performing analytical testing in line with SOPs, cGMP, and regulatory requirements
• Hands-on experience with method validation, verification, or technical transfer activities
• Strong background in data review and Good Documentation Practice (GDP)
• Demonstrated experience supporting deviation investigations, CAPA, and root cause analysis
• Previous involvement in regulatory inspections, audits, or audit readiness activities

For more information, please contact Timi Asseez.