Process Development Engineer, Manufacturing Sciences Dept
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;
* Create standard procedures for continuous improvement including non-value adding (NVA) analysis and redesign of existing standard Manufacturing Sciences procedures;
* Prepare, review and/or execute 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;
* Manage internal systems: requalification’s, periodic reviews, sample orders, trial material, process recipes, Investigation & Test Plans, 5S, product sample management and Change Records;
* 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.
Qualifications:
* Studying towards third Level Qualification in Engineering or Science.
* Knowledge of the pharmaceutical industry and pharmaceutical Oral Solid Dosage (OSD) would be preferable but not essential.
* A self-starter with initiative and good interpersonal skills is required;
* Excellent communication, report writing, time management skills and high IT proficiency;
* Attention to detail to comply with the relevant industry and Company quality standards and the cGMP rules pertaining to production.
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