By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.Job DescriptionJOB DESCRIPTIONJOB TITLE: Process Development StudentREPORTS TO: Process Development Engineer, Manufacturing Sciences DeptJOB PURPOSE:The intern will gain experience in the pharmaceutical manufacturing industry within the Manufacturing Sciences Group.RESPONSIBILITIES:Collaborate with the process engineers and compliance engineers on new product introduction (NPI) and process improvement projects;Use statistical software packages in the identification and reporting of shifts, signals and trends in critical process parameters and product quality attributes;Conduct production-based trials and studies, including in-process testing of product and creation of associated reports;Creation of standard procedures for continuous improvement including non-value adding (NVA) analysis and redesign of existing standard Manufacturing Sciences procedures;Preparation, review and/or execution of Risk Assessments, GMP assessments, Manufacturing Instructions, Annual Product Reviews and Validation Protocols / Reports;Contribute to Technical Studies, Optimisation Studies, Process, Hold Time and Cleaning Validations;Management of internal systems: requalification's, periodic reviews, sample orders, trial material, process recipes, Investigation & Test Plans, 5S, product sample management and Change Records;This position presents an exciting opportunity to work in cross functional teams with departments such as Production, Packaging, Engineering, Quality Assurance, Quality Control, Agile and Supply Chain.GENERAL RESPONSIBILITIES:Participate fully in any cross functional training initiatives;Drive and promote the corporate values of Takeda-ism within the workplace;Actively foster, in cooperation with other TIL staff, an ethos and culture of safety awareness where safety is accepted as an integral part of the overall business;Ensure timely completion of all SOP training and assessment;Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.EDUCATIONAL REQUIREMENTS:Studying towards third Level Qualification in Engineering or Science.RELEVANT EXPERIENCE:Knowledge of the pharmaceutical industry and pharmaceutical Oral Solid Dosage(OSD) would be preferable but not essential.SKILLS/COMPETENCIES:A self starter with initiative and good interpersonal skills is required;The applicant should also have excellent communication, report writing, time management skills and be highly IT proficient;Attention to detail is also required to comply with the relevant industry and Company quality standards and the cGMP rules pertaining to production.LocationsBray, IrelandWorker TypeEmployeeWorker Sub-TypePaid Intern (Fixed Term) (Trainee)Time TypeFull time