Good Manufacturing Practice

Overview

The Master of Good Manufacturing Practice from University of Technology Sydney  provides critical knowledge of legislation relating to the registration, manufacture, storage and supply of licenced therapeutic goods; GxP and quality systems compliance; and the concepts of quality management, risk management, quality assurance and quality control within this heavily regulated industry – all essential ingredients for career development. 

This being the only course of its kind in the Asia–Pacific region, the UTS: Pharmacy discipline has partnered with SeerPharma, the industry’s leading provider of technical compliance and quality assurance knowledge, to deliver students a practice-based and research-led education.

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 wishing to commence or enhance their pharmaceutical industry manufacturing career with an industry-recognised qualification.

Career options include:

• production, quality assurance, quality control, documentation, validation, supply chain and regulatory compliance in the pharmaceutical, biotechnology and medical device industry

• monitoring and quality assurance in clinical research organisations

• auditing in government regulatory agencies, consultancy in consulting firms and managers and practitioners in various other associated companies where good manufacturing practices are required.