国际学生入学条件
Applicants must have completed a UTS recognised bachelor's degree, or an equivalent or higher qualification, or submitted other evidence of general and professional qualifications that demonstrates potential to pursue graduate studies.The above qualifications must be in one of the following related disciplines: pharmacy and pharmaceutical sciences chemistry biotechnology and bioinformatics microbiology food technology, cosmetics, and nutraceutical science or medical science engineering and related technologies.Applicants who do not satisfy the above
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IDP—雅思考试联合主办方

雅思考试总分
6.5
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雅思考试指南
- 雅思总分:6.5
- 托福网考总分:79
- 托福笔试总分:550
- 其他语言考试:PTE Overall 58
CRICOS代码: 084261F
申请截止日期: 请与IDP顾问联系以获取详细信息。
课程简介
良好制造规范研究生证书提供了制药,生物技术和医疗器械行业的最新和深入的良好制造规范(GMP)知识。该课程提供有关在这个受到严格监管的行业内的法规,合规性/ GxP,产品开发和质量保证的关键知识,这是职业发展或持续学习的基本要素。悉尼科技大学(UTS):这是亚太地区同类课程中唯一的一门课程:药学学科与行业领先的技术合规性和质量保证知识提供商SeerPharma合作,为学生提供基于实践的研究主导的教育。
The Graduate Certificate in Good Manufacturing Practice provides up-to-date and in-depth good manufacturing practice (GMP) knowledge within specific fields of the pharmaceutical industry. The course provides critical knowledge regarding regulations, complianceGxP, and quality assurance within this heavily regulated industry, an essential ingredient for career development or ongoing study.The UTS: Pharmacy Discipline offers the only post-graduate qualification in GMP in the Asia-Pacific region and partners with SeerPharma, the industry’s leading provider of technical compliance and quality assurance knowledge, to deliver a practice-based and research-led education to students.Designed by leading experts in the field, the course provides professional development options and career pathways for students at all levels of industry organisations. It is ideal for students who would like to commence or enhance their pharmaceutical industry manufacturing career with an industry-recognised qualification.CareersCareer options include:Production ManagerSupervisor, Quality Assurance ManagerAssociate, Industrial Pharmacist, Quality Control Manager, Documentation Manager, Validation Manager, Supply Chain Manager, and Regulatory Affairs ManagerAssociate in the pharmaceutical, biotechnology, medical device, and allied industries.Auditor in government regulatory agencies, consultant in consulting firms, and managers and practitioners in various other associated companies where good manufacturing practices are required.
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