Carlow

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:   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:   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