C06115v3 Graduate Diploma in Good Manufacturing Practice
Award(s): Graduate Diploma in Good Manufacturing Practice (GradDipGMP)UAC code: 940921 (Calendar B Autumn session, Calendar B Spring session), 940924 (distance) (Calendar B Autumn session, Calendar B Spring session)
CRICOS code: 084262E
Commonwealth supported place?: No
Load credit points: 48
Course EFTSL: 1
Location: City campus
Notes
Due to the social distancing measures that have been introduced by the Australian Government to help slow the spread of COVID-19 within the community, the majority of UTS subjects are currently being delivered online. At this point, we expect this online delivery may continue in 2020 Spring session. We will continue to keep students updated about changes to their courses as the situation evolves.
Overview
Career options
Course intended learning outcomes
Admission requirements
Course duration and attendance
Course structure
Course completion requirements
Course program
Other information
Overview
The Graduate Diploma in Good Manufacturing Practice provides up-to-date and in-depth good manufacturing practice (GMP) knowledge within the pharmaceutical, biotechnology and medical device industries. It provides critical knowledge regarding regulations, compliance/GxP, product development and quality assurance within this heavily regulated industry, an essential ingredient for career development.
This is 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
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.
Course intended learning outcomes
| .001 | Demonstrate accurate knowledge of risk management practices and models, and implement and review them in a range of contexts. |
| .002 | Test, audit and review pharmaceuticals manufacturing and distribution processes using appropriate methodologies. |
| .003 | Implement and review process control systems for pharmaceuticals manufacturing. |
| .004 | Demonstrate ethically and legally accountable approaches to pharmaceuticals manufacturing and control. |
| .005 | Evaluate and apply evidence in the delivery of evidence-based solutions. |
| .006 | Produce accurate technical documentation, and communicate effectively and accurately with clients and stakeholders in written or spoken language appropriate to their needs. |
| .007 | Demonstrate respect and value for diverse ways of knowing, being and doing, in particular recognising the diversity of indigenous Australians, while critically reflecting on the impact of ongoing colonisation and its pervasive discourse on their health and wellbeing, and integrating this knowledge into practice. |
| .008 | Contribute as leader and collaborator in the assurance of Good Manufacturing Practice. |
| .009 | Reflect on the knowledge, skills and attributes required for the integration of emerging evidence into practice, promoting the growth of personal and professional learning, and the education of others. |
| .010 | Collaborate effectively with other professions to ensure Good Manufacturing Practice. |
| .011 | Demonstrate knowledge of Good Manufacturing Practice in local, national and global contexts. |
Admission requirements
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 academic and additional requirements may be considered on the basis of general and professional qualifications that demonstrate potential to pursue graduate studies via submission of a CV.
The English proficiency requirement for international students or local applicants with international qualifications is: Academic IELTS: 6.5 overall with a writing score of 6.0; or TOEFL: paper based: 550-583 overall with TWE of 4.5, internet based: 79-93 overall with a writing score of 21; or AE5: Pass; or PTE: 58-64; or CAE: 176-184.
Eligibility for admission does not guarantee offer of a place.
International students
Visa requirement: To obtain a student visa to study in Australia, international students must enrol full time and on campus. Australian student visa regulations also require international students studying on student visas to complete the course within the standard full-time duration. Students can extend their courses only in exceptional circumstances.
Course duration and attendance
This course is offered on a one-year, full-time or two-year, part-time basis (contact the Graduate School of Health regarding the part-time offering).
Course structure
Students must complete 48 credit points of study.
Course completion requirements
| 96057 GMP for Manufacturing Operations | 6cp | |
| 96134 Validation Principles and Practices | 6cp | |
| 96059 International GMPs and Quality Assurance | 6cp | |
| 96060 Good (Quality Control) Laboratory Practices | 6cp | |
| 96069 Contamination Control | 6cp | |
| 96062 Good Aseptic Practices and Sterile Products | 6cp | |
| 96063 GxP and Quality Auditing Practices | 6cp | |
| 96064 Risk Management for Pharmaceutical Operations | 6cp | |
| Total | 48cp |
Course program
The following example shows a typical full-time program.
| On campus, Autumn commencing, full time | ||
| Year 1 | ||
| Calendar B Autumn session | ||
| 96057 GMP for Manufacturing Operations | 6cp | |
| 96134 Validation Principles and Practices | 6cp | |
| 96059 International GMPs and Quality Assurance | 6cp | |
| 96060 Good (Quality Control) Laboratory Practices | 6cp | |
| Calendar B Spring session | ||
| 96069 Contamination Control | 6cp | |
| 96062 Good Aseptic Practices and Sterile Products | 6cp | |
| 96063 GxP and Quality Auditing Practices | 6cp | |
| 96064 Risk Management for Pharmaceutical Operations | 6cp | |
| On campus, Spring commencing, full time | ||
| Year 1 | ||
| Calendar B Spring session | ||
| 96069 Contamination Control | 6cp | |
| 96062 Good Aseptic Practices and Sterile Products | 6cp | |
| 96063 GxP and Quality Auditing Practices | 6cp | |
| 96064 Risk Management for Pharmaceutical Operations | 6cp | |
| Year 2 | ||
| Calendar B Autumn session | ||
| 96057 GMP for Manufacturing Operations | 6cp | |
| 96134 Validation Principles and Practices | 6cp | |
| 96059 International GMPs and Quality Assurance | 6cp | |
| 96060 Good (Quality Control) Laboratory Practices | 6cp | |
| Distance, Calendar B Autumn commencing, part time | ||
| Year 1 | ||
| Calendar B Autumn session | ||
| 96059 International GMPs and Quality Assurance | 6cp | |
| 96057 GMP for Manufacturing Operations | 6cp | |
| Calendar B Spring session | ||
| 96063 GxP and Quality Auditing Practices | 6cp | |
| 96064 Risk Management for Pharmaceutical Operations | 6cp | |
| Year 2 | ||
| Calendar B Autumn session | ||
| 96060 Good (Quality Control) Laboratory Practices | 6cp | |
| 96134 Validation Principles and Practices | 6cp | |
| Calendar B Spring session | ||
| 96069 Contamination Control | 6cp | |
| 96062 Good Aseptic Practices and Sterile Products | 6cp | |
| Distance, Calendar B Spring commencing, part time | ||
| Year 1 | ||
| Calendar B Spring session | ||
| 96064 Risk Management for Pharmaceutical Operations | 6cp | |
| 96063 GxP and Quality Auditing Practices | 6cp | |
| Year 2 | ||
| Calendar B Autumn session | ||
| 96059 International GMPs and Quality Assurance | 6cp | |
| 96057 GMP for Manufacturing Operations | 6cp | |
| Calendar B Spring session | ||
| 96069 Contamination Control | 6cp | |
| 96062 Good Aseptic Practices and Sterile Products | 6cp | |
| Year 3 | ||
| Calendar B Autumn session | ||
| 96060 Good (Quality Control) Laboratory Practices | 6cp | |
| 96134 Validation Principles and Practices | 6cp | |
Other information
Further information is available from:
Graduate School of Health
telephone +61 2 9514 1448
email gsh.future@uts.edu.au