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.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.r-dpartners.com/privacy-policy/

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Responsibilities

About the job

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.