Master's Degree Pharmacy Full Time

Master of Good Manufacturing Practice

at University of Technology Sydney · Sydney, New South Wales

CRICOS course code

084264C

CRICOS provider code

00099F

This course is registered on the Commonwealth Register of Institutions and Courses for Overseas Students. Verify it yourself at cricos.education.gov.au before paying any fee.

Duration

2 years

Tuition (whole course)

A$84,020 total

Per year

A$42,010/yr

Intake

Semester 1 (Feb/Mar), Semester 2 (Jul)

About this program

The Master of Good Manufacturing Practice at the University of Technology Sydney is designed for professionals aiming to deepen their expertise in the principles and practical applications of good manufacturing practice (GMP) within the healthcare, pharmaceutical and medical device sectors. Delivered over two years in Sydney, this master’s degree provides advanced understanding of quality assurance, regulatory compliance, risk management, and validation processes that underpin safe and effective manufacturing in the life sciences.

The programme typically comprises a series of units of study, each assigned a set number of credit points, allowing students to progress through a mix of core and elective subjects. You will gain skills in auditing, quality management systems, and current industry standards, culminating in a research project or capstone activity. This authentic learning experience is structured to include work-integrated learning opportunities, such as case studies or professional placement, enabling you to apply classroom knowledge in real-world industry contexts.

The course empowers graduates with advanced competencies in regulatory requirements, documentation, quality control, and leadership in GMP environments. It is ideally suited for those seeking career advancement in pharmaceutical manufacturing, biotechnology, or related fields, as well as for professionals transitioning into the regulatory or quality assurance sectors of the healthcare industry. Students benefit from UTS’s strong industry links and the course’s emphasis on contemporary Australian and international GMP frameworks.

International students enrolled in this degree are eligible for up to 48 hours of work per fortnight, providing valuable exposure to Australia’s robust healthcare and life science industries. Graduates may also be eligible for the Temporary Graduate (subclass 485) visa post-study work stream. For details about admission requirements, application processes, and accreditation, refer to the official course page.

Entry requirements

English: International applicants must evidence English proficiency. IELTS Academic 6.0–6.5 overall is the common undergraduate and coursework-postgraduate standard, rising to 7.0–7.5 for teaching, nursing, medicine, law and social work. TOEFL iBT, PTE Academic, Cambridge C1 Advanced and the university’s own English programmes are accepted as equivalents; the Department of Home Affairs sets a separate English threshold for the Student visa itself.
International students: Registered on CRICOS for international students. A Confirmation of Enrolment (CoE) for this course supports a Student visa (subclass 500) application; Overseas Student Health Cover is required for the full duration.

Career outcomes

  • Quality Assurance Manager in pharmaceutical or biotechnology companies
  • Regulatory Affairs Specialist
  • GMP Compliance Auditor
  • Validation Specialist in medical device or manufacturing sectors
  • Production Supervisor in Australian life sciences industries
  • Process Improvement Analyst in healthcare manufacturing

Frequently asked questions

How long is the Master of Good Manufacturing Practice at University of Technology Sydney?

It typically takes 2 years, with intakes in Semester 1 (Feb/Mar), Semester 2 (Jul).

How much is the tuition?

Tuition is around A$84,020 total. Fees change yearly — confirm with an advisor.

What are the career outcomes?

Quality Assurance Manager in pharmaceutical or biotechnology companiesRegulatory Affairs SpecialistGMP Compliance AuditorValidation Specialist in medical device or manufacturing sectorsProduction Supervisor in Australian life sciences industriesProcess Improvement Analyst in heal...

Guides for this subject and the application

All guides →

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