A company who specialises in photopheresis technology and has been providing ECP (Extracorporeal Photopheresis) solutions in Dublin. They are looking for a Labelling Engineer who can create all new/revised artwork for the labelling team and oversee and manage all new/revised operator manuals, technical bulletins, device labels, graphic arts, and labelling documentation approval across all device development programs. The ideal candidate would be someone with In depth illustrator and InDesign knowledge and a strong labelling and graphic design background. This will be a hybrid role in Dublin but further into the role this will move to 1-2 days max in the office. #J-18808-Ljbffr
Reporting to: Senior Manager, Technical Operations. As an RFT Operations Specialist, you serve as the critical link between Technical Operations and Manufacturing, ensuring sterile production activities are executed Right First Time by being present on the shop floor during key stages to provide real‑time technical support, guide operators through process steps and documentation, troubleshoot deviations and unexpected events, and maintain strong GMP and batch‑record compliance. You draft, review, and refine technical protocols and batch records, support audits and documentation integrity, deliver operator training on essential processes, and actively promote a strong quality culture across production teams. Experience Hands‑on experience as an Operator or Operator Lead in pharmaceutical/sterile manufacturing Strong understanding of aseptic processing , contamination control , and sterile environments Familiarity with unit operations (e.g., lyophilisation , filtration , centrifugation , autoclaves ) Comfortable working on the shop floor and supporting on‑call activities Excellent communication skills and ability to guide operators in real time #J-18808-Ljbffr
A leading pharmaceutical company in Dublin seeks an RFT Operations Specialist to act as a critical link between Technical Operations and Manufacturing. The candidate will ensure sterile production activities are executed correctly and provide real-time technical support on the shop floor. Responsibilities include drafting and refining technical protocols, supporting audits, and conducting operator training. The ideal candidate will have strong experience in aseptic processing and contamination control in a sterile environment. #J-18808-Ljbffr
A key role responsible for maintaining and improving Quality Management Systems, leading investigations, and supporting site‑wide compliance and continuous improvement initiatives. Key Responsibilities Lead and support investigations relating to quality events and provide clear recommendations Oversee CAPA activities and ensure effective follow‑through Analyse and report trends within the Quality Management System Review and approve procedures, reports, and protocols Participate in audits as a subject‑matter expert or lead auditor Contribute to site‑wide projects and continuous improvement initiatives Support day‑to‑day QA operations and team workload Required Experience & Skills Bachelor’s degree in a scientific discipline 4+ years’ experience in a cGMP environment, ideally within QA Strong communication, problem‑solving, and decision‑making abilities Experience with regulatory requirements and cGMP expectations Competence in statistical analysis and technical writing #J-18808-Ljbffr
A prominent consulting firm in Dublin seeks a Quality Assurance professional to lead and support investigations into quality events and to enhance Quality Management Systems. The ideal candidate will have a Bachelor's degree in a scientific discipline, coupled with over 4 years of experience in a cGMP environment and strong communication skills. Key responsibilities include overseeing CAPA activities, analyzing trends, and participating in audits. This role is pivotal for ensuring compliance and continuous improvement across site-wide operations. #J-18808-Ljbffr
