Manufacturing Technologist

Manufacturing TechnologistPostuler: Dublin: Temps complet: Offre publiée aujourd'hui: R-22445 Titre : Manufacturing Technologist Société: Ipsen Manufacturing Ireland Ltd A propos d'Ipsen: Ipsen est un groupe biopharmaceutique mondial de taille moyenne, spécialisé dans les médicaments transformateurs dans trois aires thérapeutiques : l'oncologie, les maladies rares et les neurosciences. Forts de près de 100 ans d'expérience en développement, avec des Hubs mondiaux aux États-Unis, en France et au Royaume-Uni, nous focalisons nos efforts là où les besoins médicaux non satisfaits sont importants, grâce à la recherche et à l'innovation.Nos équipes passionnées, présentes dans plus de 40 pays, se concentrent sur l'essentiel et s'efforcent chaque jour d'apporter des médicaments aux patients dans 88 pays. Nous construisons un environnement de travail qui met en avant un leadership centré sur l'humain et favorise une culture de collaboration, d'excellence et d'impact. Au sein d'Ipsen, chaque individu est encouragé à être soi-même, à grandir et à s'épanouir aux côtés du succès de l'entreprise. Rejoignez-nous dans notre démarche vers une croissance durable, en créant un impact réel sur les patients et la société.Pour plus d'informations, visitez notre site web à l'adresse et suivez nos dernières actualités sur LinkedIn et Instagram . Description de l'emploi : Ready to make an impact in a fast-paced manufacturing environment? Due to business demands and capacity increase requirement, we are seeking enthusiastic and detail-focused individuals to join our Blanchardstown manufacturing facility as Manufacturing Technologists, working 3 x 12 hr. shift premium- 38.5h in a three-week cycle (weekend nights). This 18-month fixed-term position is an excellent opportunity for anyone eager to build experience in pharmaceutical manufacturing. The role provides hands-on training, a 25% weekend shift allowance, and the chance to develop valuable industry experience. About the role This weekend shift position plays a key role in maintaining continuous manufacturing operations and supporting overall site production throughput. As a member of the dedicated weekend team, you will ensure the seamless execution of GMP-compliant processes across multiple manufacturing platforms. Working within a regulatory environment, you will support both upstream and downstream processing activities and receive cross-functional training across Synthesis, Purification, and Cleanroom operations. This exposure offers the opportunity to develop a broad technical skillset and contribute directly to the manufacture of high-quality therapeutic products. Participate in structured training across both downstream and upstream operations. This initiative aims to build cross-functional knowledge and enhance operational flexibility. Key Responsibilities: Execute daily production operations as directed by the Shift Lead and/or Manufacturing Manager, ensuring productivity, timeliness, and cost-efficiency while adhering to GMP and EHS standards. Oversee prompt and accurate completion of all batch related documentation Performs daily production operations, as outlined by the shift lead and/or manufacturing manager, with a view to meeting the overall objectives of productivity, timeliness and cost while following GMP and EHS expectations. Carry out routine cleaning, sanitisation, and environmental control procedures. Support upstream and downstream activities, including synthesis, purification & lyophilisation. Complete batch record documentation and in-process checks in line with GMP standards, with a focus on submission to quality in a timely manner. Assist with equipment setup, operation, calibration, and troubleshooting. Participate in SOP revisions and continuous improvement initiatives. Adhere to all EHS and safety procedures, including risk assessments and deviation reporting. Rotate across functional areas (Synthesis, Purification, Cleanroom) as required to support production schedules and site priorities. Ensure high standards of housekeeping are maintained in the area Work Pattern: Three -week cycle on rotation Week 1 Friday - Sunday: 19:00 - 07:00Monday: Rest Day Week 2 Friday - Sunday: 19:00 - 07:00Monday: Rest Day Week 3 Friday - Sunday: 19:00 - 07:00Monday: 19:00 - 02:30 Qualifications & Experience Minimum: Working knowledge of cGMP, EHS, and operational excellence principles. Ability to work both independently and collaboratively in a fast-paced, regulated environment. Demonstrated adaptability and teamwork across functional areas. Strong documentation accuracy and communication skills. Preferred: Diploma in science related discipline, Ideally BSc. in science. 2+ years' experience in a GMP-regulated environment. Familiarity with processing equipment, automation systems and peptide manufacturing. Experience with MES, SAP, and electronic batch record systems. Knowledge of Operational excellence and/or Lean Six Sigma.If you have the right qualification and/or relevant experience, and you're ready to grow your skills in a GMP manufacturing environment, we'd love to hear from you.