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 Description** **JOB DESCRIPTION** **_JOB TITLE:_** **Process Development Student** **_REPORTS TO:_** **Process Development** **Engineer, Manufacturing Sciences Dept** **_JOB 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. **Locations** Bray, Ireland **Worker Type** Employee **Worker Sub-Type** Paid Intern (Fixed Term) (Trainee) **Time Type** Full time