Graduate Diploma in Good Manufacturing Practice – UTS

Graduate Diploma Pharmacy Full Time

Graduate Diploma in Good Manufacturing Practice

at University of Technology Sydney · Sydney, New South Wales

CRICOS course code

084262E

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

1 year

Tuition (whole course)

A$42,010 total

Per year

A$42,010/yr

Intake

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

About this program

The Graduate Diploma in Good Manufacturing Practice at the University of Technology Sydney is tailored for professionals seeking to advance their expertise in pharmaceutical, biotechnology, and related industries. The course provides a comprehensive understanding of good manufacturing practice (GMP) regulations and their crucial role in ensuring product quality, safety, and compliance in Australia and globally. It is aligned with the evolving regulatory environment and industry expectations, with a strong focus on current trends, standards, and ethical considerations.

This graduate diploma is delivered over 1 year of full-time study, structured around progressive units of study that amount to a specific number of credit points as stipulated by the university. The curriculum covers topics such as quality assurance, regulatory compliance, validation processes, risk management, and documentation systems, all vital for modern manufacturing environments. Students also engage with practical and case-based learning, gaining critical problem-solving and decision-making skills relevant to the Australian and international pharmaceutical landscape.

Throughout the programme, emphasis is placed on work-integrated learning to connect academic knowledge to real-world applications. Delivered in Sydney, a key hub for Australia's pharmaceutical and life sciences sectors, students benefit from the university's industry connections, gaining insights from practitioners and exposure to professional practices.

The course is especially well-suited to graduates in pharmacy, chemistry, biological sciences, engineering, or related fields, as well as professionals already employed in regulated industries who are seeking to formalise or further their knowledge in GMP. Domestic and international students can capitalise on Australia's work rights during study (48 hours per fortnight) and, upon graduation, become eligible to apply for the Temporary Graduate visa (subclass 485) post-study work stream. All candidates should confirm entry requirements and course structure via the official programme 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 Officer in the pharmaceutical and biotechnology industries
Regulatory Affairs Associate
Production Supervisor in manufacturing facilities
Validation Specialist
Compliance Auditor
Roles in Australian government health and regulatory agencies
Positions in contract manufacturing and research organisations

Frequently asked questions

How long is the Graduate Diploma in Good Manufacturing Practice at University of Technology Sydney?

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

How much is the tuition?

Tuition is around A$42,010 total. Fees change yearly, confirm with an advisor.

What are the career outcomes?

Quality Assurance Officer in the pharmaceutical and biotechnology industriesRegulatory Affairs AssociateProduction Supervisor in manufacturing facilitiesValidation SpecialistCompliance AuditorRoles in Australian government health and regulatory agenciesPositions in contract manuf...

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