Careers

Role Summary:   The Technology Transfer/Process Engineer will provide key technical leadership and support in the areas of new product introduction, development batch planning/execution and product launch activity technical support. The successful candidate will ensure that a TT/NPI plan is developed, and all required documentation is generated to support same. They will work cross functionally

Role Summary:   A new opportunity has arisen for an experienced Process Engineer at our client’s pharmaceutical site in Athlone, Co. Westmeath. The successful candidate is responsible for the performance of the process equipment on site. The Process Engineer will provide key technical support in the areas of yield improvement, reliability, process control, manufacturing process

Role Summary:   A fantastic opportunity has arisen for a Manufacturing Support Specialist at our client’s busy pharmaceutical site in Athlone, Co. Westmeath. Reporting to the Senior Manufacturing Manager, the role will provide technical leadership and support to the packaging manufacturing area. The core focus will be to work with operations, engineering and quality personnel

Role Summary:   Our client’s External Manufacturing (ExM) Technical Operation organization is seeking a highly motivated individual for a Technical Transfer position at their site in Co. Cork. ExM Tech Ops is accountable for technology transfers and commercial production of Biological Drug Substance at their External Partners (EPs). The successful candidate will have the opportunity

Role Summary:   We are currently recruiting for a Senior Process Engineer to join our Process Department in our thriving Cork office. Delivery of projects from concept through to full detail design stages. Activity planning, work scheduling, assigning responsibilities to the team, and ensuring deliverables can be met.   Core Duties and Responsibilities:   Lead the

Role Summary:   A vacancy has arisen for the role of a Project Scheduler at our client’s pharmaceutical site in Co. Cork. The successful candidate will play an integral role in providing Project Scheduler Support to the Restructuring Decommissioning Team. The individual will also be giving support to the Product Deletions Team for project related

Role Summary:   A new opportunity has arisen for an experienced Automation Engineer II at our client’s busy pharmaceutical site in Co. Tipperary. The successful candidate will be a member of the Automation & PI/MES team reporting to the Site Manufacturing Systems Lead, specifically responsible for both project support and fault-finding / support of production

Role Summary:   A vacancy has arisen for the role of an IT Business Analyst at our client’s busy pharmaceutical site in Co. Tipperary. Reporting to the Site IT Lead, the successful candidate will provide technical and business support on overall maintenance & development of assigned IT Applications and Systems and participate in divisional initiatives

Role Summary:   The Validation Engineer will design, coordinate and execute validation activities in support of the start-up manufacturing facility, and will be responsible for on-going re-validation of equipment and processes when the facility transitions from start-up mode to commercial supply. The Validation Engineer reports to the Technical Services Manager.   Duties:   Develops and

Role Summary:   A new opportunity has arisen for a QC Documentation/Administration Specialist at our client’s pharmaceutical site in Co. Dublin. The successful candidate will be responsible for supporting the Quality Control Department in the management of department documentation, and support of the QC functions through various administrative duties. The individual will ensure that objectives

Role Summary:   An amazing opportunity has arisen for a Learning and Development Business Partner at our client’s busy pharmaceutical site in Co. Meath. Reporting to the Learning and Development Lead, the successful candidate will be responsible for deliverables within the learning management system implementation as part of a larger Integration project. This candidate will

Role Summary:   A vacancy has arisen for the role of a Commissioning, Qualification and Validation (CQV) Quality Assurance Specialist at our client’s new state-of-the-art facility in Co. Meath. The successful candidate will play an integral role in providing Quality oversight on the design and qualification activities as part of the design, construction, qualification and

Role Summary:   The Project Manager is responsible for managing delivery of Project deliverables, the consistency, visualization and management of the project execution through effective communication plans and stakeholder management via the Governance Process. Key responsibilities for the Project Manager will be to engage and work collaboratively across site teams to ensure the projects are

Role Summary:   A new opportunity has arisen for a Manufacturing Specialist at our client’s busy pharmaceutical site in Co. Meath. The successful candidate will work in a manufacturing self-directed days team supporting a team of Manufacturing Biotech Associates. The Manufacturing Specialist will support the team to deliver the operational start up activities to ensure

Role Summary:   This role will support the Quality Control SDWT/Hub for testing of incoming raw materials, in-process drug substance/drug product, final drug products, stability samples and environmental monitoring of the controlled manufacturing areas and utilities at our client’s new single use multi-product biotech facility in County Meath, Ireland. This facility will manufacture antibody-based therapies.

Role Summary:   A vacancy has arisen for the role of a Manufacturing Engineer for our client’s state-of-the-art facility in Co. Wexford. As a Manufacturing Engineer, you will assist with all engineering activities relating to the introduction of a new product being manufactured and you will perform tasks associated with these activities including the key

Role Summary:   A new opportunity has arisen for a Document Controller to support our client’s Quality Systems Team based in Co. Meath. Reporting to the QA Systems Lead, the Document Controller role will be primarily involved in supporting Document Management (Paper based and electronic) activities on site. All relevant activities on site are conducted in

Role Summary:   A fantastic opportunity has arisen for a Senior Talent Acquisition Advisor to join our client’s Talent Team in Dublin. This role will require occasional travel to other sites across Dublin, Meath and Carlow.   Core Duties and Responsibilities:   Partner with the business to understand priority needs, support the hiring of niche

Role Summary:   A new opportunity has arisen for the role of a Clean Support Utilities Engineer at our client’s busy pharmaceutical site in Co. Carlow. The successful candidate will provide technical expertise within the Engineering group to deliver the maintenance program for side wide utilities systems and its associated infrastructure. The individual will also

Role Summary:   A vacancy has arisen for a QC Microbiology Technician to join our client’s Quality team at their pharmaceutical site in Co. Carlow. The successful candidate will perform day to day laboratory testing, data review, routine duties and be capable of enthusiastically taking responsibility for ad-hoc duties and projects. While working cooperatively as

Role Summary:   A vacancy has arisen for the role of a Senior OEM Engineer at our client’s busy pharmaceutical site in Co. Carlow. Senior OEM Engineer, reporting to the site AIT OEM Lead, specifically responsible for OEM Systems. This candidate will be required to work closely with the site AIT teams responsible for the

Role Summary:   Reporting to the Associate Director Technical Engineering (CPEG), as Project Engineer you will lead and manage multiple Technical Engineering projects from scope development, design, build/install and qualify through to handover to operations for key Technical Engineering projects at our client’s site in Co. Carlow. This includes but is not limited to Process

Role Summary:   As part of the Technical Transfer team you will be responsible for the transfer of a syringe and/or vial commercial product from the client’s existing lines to the newly expanded facility, as well as the transfer of a formulation process from a US site to Co. Carlow site. As part of your

Role Summary:   Our client is looking for an experienced Quality Engineer with New Product Introduction experience for their state-of-the-art facility in Co. Wexford. The Quality Engineer will assure that new products and the processes for manufacturing them meet all local, Corporate and Divisional requirements with respect to safety and efficacy.   Core Duties and

Role Summary:   Primary focus of this position is to support in developing, optimizing, implementing, and validating components/elements of a medical device. The candidate will perform hands-on testing in optimization of a device; conduct process development activities to understand process inputs and outputs; assist/write technical documents, validation protocols and reports; prepare work instructions and standard

Role Summary:   A vacancy has arisen for the role of a Quality Assurance Specialist at our client’s busy pharmaceutical site in Co. Carlow. The Quality Assurance Specialist is required to: Work a 4 shift pattern role Technical knowledge of sterile manufacturing processes Perform timely reviews of batch documentation / investigations / reports highlighting and assist

Role Summary:   The successful candidate will be responsible for providing process, technical, and validation support operations including ongoing support of manufacturing processes and support for new product introduction. Accountable for analytical/engineering studies associated with the development of new components, products, processes systems and facilities. Co-ordination, design and execution of equipment qualification and validation as

Role Summary:   The successful candidate will work within the supply chain Materials and SAP team at our client’s busy pharmaceutical site in Co. Carlow. They will be responsible for the material management Process. Primary responsibility will be for the management and co-ordination of New Material Introduction (NMI) Process. Contributing to the site clinical and

Role Summary:   The successful candidate will work within the supply chain Materials and SAP team at our client’s busy pharmaceutical site in Co. Carlow. This individual will be responsible for initiating and managing supplier complaints. This requires review and progress of the complaints at the site cross-functional MRB meeting and liaising with Supplier Performance and

Role Summary:   The successful candidate will work within the supply chain Materials and SAP team at our client’s busy pharmaceutical site in Co. Carlow. This individual will be responsible for the Supplier Change notification Process. Primary responsibility will be for the management, ownership and co-ordination of Supplier changes. Clear understanding of change notification process

Role Summary:   The successful Electrical Design  Engineer will be responsible for the design, implementation and handover of multidisciplinary engineering projects. This role can be based in our Cork or Kilkenny office.   Core Duties and Responsibilities:   Management of the design, implementation and handover of multi-disciplinary engineering projects; focusing on electrical requirements, utilities, automation

Role Summary:   A vacancy has arisen for an experienced Process Engineer on our client’s busy pharmaceutical site in Waterford. As a Process Engineer you will provide leadership and support to the vial inspection team to ensure appropriate standards are met. You will be involved in the development and implementation of improvement initiatives in vial

Role Summary:   A vacancy has arisen for the role of a Quality Control (QC) Instrumentation Systems Specialist at our client’s busy pharmaceutical site in Dublin. The successful candidate will operate as part of a dynamic team to plan, execute, and managing the activities required to maintain the testing infrastructure of the QC lab. The

Role Summary:   A new opportunity has arisen for an experienced Project Manager to join our client’s Project Management Office in Co. Dublin. The role is of key importance to the PMO function and risk management team on site.   Core Duties and Responsibilities:   Project management of selected projects within the site’s project portfolio,

Role Summary:   Drive Process Understanding, Capability and Continuous improvement projects to support the site strategy, delivering safe, compliant and robust operations from a Process Engineering perspective. Involved in, process design and generating innovative engineering solutions to drive continuous improvement.   Core Duties and Responsibilities:   Provide technical leadership in the application of process engineering

Role Summary:   Our client is looking for a QC Chemist based in Co. Waterford. The successful applicant will become a member of the in-process QC Chemistry team onsite. The in-process QCC team supports the aseptic filling lines with activities including cleaning verifications, bulk product identifications, water analysis and analysing foreign matter and glass damage

Role Summary:   A vacancy has arisen for an experienced Automation Engineer to support our client’s Automation Team in Waterford. The successful candidate will play an integral role in providing automation support and expertise across multiple departments on a busy pharmaceutical site.   Core Duties and Responsibilities:   Work with the Automation Team to provide

Role Summary:   The Capital Project Team (CPT) is looking for an experienced start up Project Manager to help lead the planning, readiness and execution of a New Product introduction at our client’s new Biologics facility. With your help we will ensure success by clearly defining, coordinating, managing and tracking the scope required to deliver

Role Summary   The QC Microbiology Analyst role is a critically important activity, ensuring efficient and effective compliant design, construction, qualification, and operation of our client’s Drug Substance facility in Co. Dublin. This position will be responsible for qualifying the Microbiology Quality Control lab and the transfer of Microbiological analytical methods including but not limited

Role Summary:   Our client is looking for a Compliance Documentation Specialist. The Compliance Documentation Specialist will provide compliant, accurate and timely support to the client’s Supply Chain team.   Core Duties and Responsibilities:   The Compliance Documentation Specialist is accountable for the smooth execution of all appropriate documentation associated within the SCM Warehouse team.

Role Summary:   Our client’s External Manufacturing (ExM) Technical Operation organization is seeking a highly motivated individual for a Technical Transfer position. ExM Tech Ops is accountable for technology transfers and commercial production of sterile drug product at their External Partners (EPs). This person will have the opportunity to participate in all these areas. This

Role Summary:   Our client is seeking a highly motivated individual for a Technical Transfer position in their External Manufacturing (ExM) Technical Operation organization. ExM Tech Ops is accountable for technology transfers and commercial production of sterile drug product at their External Partners (EPs). This person will have the opportunity to participate in all these

Role Summary:   A vacancy exists within our client’s Global Engineering Solutions (GES) group for a Senior Project Engineer supporting GES capital projects in Co. Tipperary, Ireland. Reporting to the Global Engineering Solutions Project Manager based at the Co. Tipperary Site. This will be a key role in the GES organization which is currently executing

Role Summary   The Projects Process Engineer is a crucial role within the Project department to ensure the introduction of new equipment and processes and to perform technical development of existing processes. Working in a highly regulated and cGMP environment within the pharmaceutical industry the Projects Process Engineer will report directly to the Project Manager

Role Summary:   An opportunity has arisen in our client’s Quality team for an experienced Qualified Person supporting the Spray Dried Intermediate Drug Product and final formulated Drug Product Formulation Facilities.   Core Duties and Responsibilities:   As a site SME for batch disposition, lead the Drug Product Intermediate and final Drug Product quality release

Role Summary:   The Engineering Department is seeking a Project Engineer to support site Capital & Expense projects. This is an exciting opportunity to work for a leading pharmaceutical company in the South East of Ireland.   Core Duties and Responsibilities:   To support the engineering requirements through managing & liaising with key project stakeholders

Role Summary:   The Engineering Department is seeking a Construction Supervisor to support site Capital & Expense projects. This is an exciting opportunity to work for a leading pharmaceutical company in the South East of Ireland.   Core Duties and Responsibilities:   Overall responsibility for the development and management of the Construction Service business delivered

Role Summary:   The Engineering Department is seeking an Electrical Project Engineer to support site Capital & Expense projects. This is an exciting opportunity for an Electrical Engineer to work for a leading pharmaceutical company in the South East of Ireland   Core Duties and Responsibilities:   To support the engineering requirements through managing &

Role Summary   The MMDIT Lead Engineer for labs will be responsible for delivery of Automation and IT scope on one or more lab projects in the portfolio of capital projects managed.  This candidate will be required to work closely with the MMDIT teams responsible for the full Automation and IT scope and with vendors

Role Summary:   As part of a significant expansion an exciting opportunity has come to join the Validation team to transition from a project phase to a fully operational facility delivering life-saving products to patients. Each role will be involved in the project from the vendor Factory Acceptance Test (FAT), at the earliest, through to