Process Development Engineer Student
応募 後で応募 求人ID R0163265 掲載日 09/19/2025 Location:Wicklow, IrelandBy 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 Noticeand 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.