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Research & Development Engineer

Role Purpose: An exciting opportunity has arisen for a Research and Development Engineer to join our client’s busy pharmaceutical site in Co. Waterford. Supporting product development & process development activities, writing protocols, data gathering and analysis.   Core Duties and Responsibilities: Support new produce/process validations. Design, execute, and analyze experiments. Support existing manufacturing processes, quality improvements […]

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Validation Engineer

Role Purpose: A fantastic opportunity has arisen for a Validation Engineer to join our client’s biopharmaceutical facility in Co. Waterford. In the Validation Engineer role, you will be required to support new product introductions, equipment qualification and the site requalification program. The Validation Engineer has a key role in ensuring the on-going validation and compliance […]

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Process Engineer

Role Purpose: A new opportunity has arisen for a Process Engineer to join our client’s biopharmaceutical facility in Co. Waterford. The Successful candidate will provide Process Engineering support to existing business as usual daily functions and on-going continuous improvement pre-filled syringe processes. Support in the manufacturing of monoclonal antibody (mAb) commercial products, support technology transfer […]

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Senior Maintenance Technician (shift)

Role Purpose: An exciting opportunity now exists at our client’s biopharmaceutical facility based in Co. Waterford for an experienced Senior Maintenance Technician. The Senior Maintenance Technician will be reporting to the Technical Team Lead. As a Maintenance Technician, you’ll play an important role in being a maintenance subject matter expert in all systems associated with […]

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QC Stability Specialist

Role Purpose: An exciting new vacancy has arisen for a QC Stability Specialist to join our client’s busy biopharmaceutical facility in Co. Waterford. The QC Stability Specialist will be responsible of the management of stability programs including generation of protocols and reports, sample management, compilation of results and communication to both internal and external stakeholders. […]

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QC Chemist

Role Purpose: Our client, based in Co. Waterford, is looking for a QC Chemist to join their busy biopharmaceutical facility. The QC Chemist will be providing analytical chemistry services and support to Site.   Core Duties and Responsibilities: Effective interaction with other departments on matters related to raw materials, intermediates and finished batch releases. In […]

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Equipment Project Engineer

Role Summary: Our client is looking for an accountable Project Engineer to deliver a diverse project portfolio assignment at their Waterford facility. Delivery of this project portfolio will be within their biopharmaceutical operations which include enzyme, monoclonal antibodies (mAbs), oral dosage, medical device, laboratories & packaging operations. The successful candidate will schedule, plan, forecast, resource […]

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QC IT Systems Engineer

Role Summary: Our client is seeking a highly skilled and experienced IT Engineer specialising in Quality Control (QC) of equipment and instruments to join their pharmaceutical site in Co. Waterford. The successful candidate will be responsible for managing, maintaining, and optimizing all IT aspects of the QC laboratory equipment to ensure maximum efficiency and compliance […]

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QA Specialist

Role Summary: Our client is looking for a Quality Assurance Specialist to join their QA Team based at their busy biopharmaceutical facility in Co. Waterford. The successful candidate will be a critical team member, reporting directly to the Quality Compliance Team Leader and will play an integral role within Quality Assurance to support for projects. […]

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Quality check illustration

Quality Systems Specialist

Role Summary: A new vacancy has arisen for a Quality Systems Specialist to join our client’s Quality Systems Team based at their busy biopharmaceutical facility in Co. Waterford. The Quality Systems Specialist will ensure that effective quality systems are implemented meeting industry standards and all cGMP requirements. The successful candidate will report to the Quality […]

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