良好制造规范硕士提供了制药，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。本课程提供与法规有关的重要知识，包括与注册的治疗产品的注册，制造，存储和供应，GxP和质量体系合规性，以及在这个受到严格监管的行业中的质量管理，风险管理，质量保证和质量控制的概念– “职业发展的所有基本要素。
The Master of Good Manufacturing Practice provides up-to-date and in-depth good manufacturing practice (GMP) knowledge, skills, and experience within the pharmaceutical, biotechnology, and medical device industries. The course provides students with critical knowledge and the ability to evaluate and apply legislation relating to the registration, manufacture, storage, and supply of licensed therapeutic goods, GxP and quality systems compliance, and the concepts of quality management, risk management, aseptic practices, supply chain, clinical trials, quality assurance, and quality control within this heavily regulated industry all essential ingredients for career development.<br>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.<br><br>Designed by leading experts in the field, the course provides students with professional development options and career pathways 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.<br>Career options include:<br>Production Manager/ Supervisor, Quality Assurance Manager/ Associate, Industrial Pharmacist, Quality Control Manager, Documentation Manager, Validation Manager, Supply Chain Manager, and Regulatory Affairs Manager/Associate in the pharmaceutical, biotechnology, medical device, and allied industries.<br>Auditor in government regulatory agencies, consultant in consulting firms, and managers and practitioners in various other associated companies where good manufacturing practices are required.