Master of Science in Pharmaceutical Quality Assurance & Regulation

Integrated Masters with deeper specialization and research focus
Taught in English
Duration 1.5 Years
Mode On Campus
Level Postgraduate
Degree Masters Degree
Next Intake TBA

Course Overview

The Master of Science in Pharmaceutical Quality Assurance & Regulation at Technological University Dublin is designed for science graduates seeking to specialise in the critical demands of the pharmaceutical and biopharmaceutical sectors. You will gain a comprehensive understanding of quality assurance, auditing, and manufacturing processes, preparing you to navigate the complex regulatory landscape. This postgraduate degree is ideal if you aim to bridge your scientific background with the specific, high-stakes requirements of ensuring drug safety and efficacy in a globally regulated industry.

This full-time, on-campus programme is studied over 18 months, integrating theoretical knowledge with practical application. You will explore advanced therapeutics, biopharmaceutical manufacturing, pharmaceutical technologies, and quality risk management, culminating in a significant dissertation project in your second year. You will work alongside experienced academics and gain insights into pharmaceutical regulation and validation. Graduates are equipped for impactful roles in quality assurance, regulatory affairs, and compliance within the pharmaceutical industry worldwide.

Course Curriculum & Details

Detailed information for serious evaluators

Program Overview

This Master of Science program provides a comprehensive understanding of pharmaceutical quality assurance and regulatory affairs. Students will explore advanced therapeutics, biopharmaceutical manufacturing processes, and pharmaceutical technologies. The curriculum also covers essential areas such as pharmaceutical microbiology, aseptic manufacturing, quality risk management, and regulatory compliance, culminating in a dissertation.

1 Year One / Semester 1

Advanced therapeutics and their regulation Mandatory
Advanced therapeutics and their regulation Mandatory
Biopharm Manufacture drug production Mandatory
Pharmaceutical Quality Assurance & Research Methods Mandatory
Pharmaceutical Technologies (Process, Facility, Equipment & Utilities) Mandatory

2 Year One / Semester 2

Pharmaceutical Manufacturing and Management Mandatory
Pharmaceutical Microbiology and Aseptic Manufacture Mandatory
Pharmaceutical Regulation, Validation & Statistics Mandatory
Innovative Medicines and their regulation Mandatory
Quality Risk Management Mandatory

3 Year Two / Semester 1

Dissertation Mandatory

Cost & Affordability

A clear picture of what this course will cost you

Program Costs

First Year Fee Tuition fee
USD 12,793.00
Second Year Fee Tuition fee
USD 12,793.00
Total Program Cost Estimated total tuition
USD 25,586.00

Currency note: Program costs shown in USD based on the available tuition breakdown.

Living Costs

Accommodation
USD 644.00 - USD 3,372.00
Food & Groceries USD 3,930.00 - USD 5,613.00
Transport USD 842.00 - USD 1,965.00
Utilities & Bills USD 1,404.00 - USD 2,105.00
Estimated Total USD 6,176.00 - USD 9,683.00

Living cost estimates are based on Grangegorman Campus.

Outcomes & Employability

What happens after you graduate

86%
Graduate Employment Rate Within 6 to 12 months of graduation

Common Graduate Roles

Biotechnology & GenomicsCurriculum & Instructional DesignDrug Discovery & ResearchEarly Childhood & Primary EducationEducation Policy & AdministrationEducational Support ServicesHealthcare ConsultingQuality Assurance & ControlSales & Medical AffairsSpecial & Inclusive Education

Top Employers Hiring for this course

Health Service Executive

Mater Misericordiae University Hospital

Pfizer

St James's Hospital Dublin

Why Study Master of Science in Pharmaceutical Quality Assurance & Regulation at Technological University Dublin

What makes this program stand out

Top 20 in UK For Computer Science

Exeter's Computer Science department consistently ranks among the top 20 in the UK for both teaching quality and research output.

Fast Offers Quick turnaround

Exeter typically responds to applications within 2-3 weeks, giving you clarity on your options quickly.

Flexible Intakes September start

Primary intake in September with January start available for some pathways through the INTO foundation program.

Accredited Industry recognized

Accredited by BCS, The Chartered Institute for IT, meeting requirements for Chartered IT Professional (CITP) status.

Life at Technological University Dublin in Ireland

What daily life looks like for international students

Language

English

Primary language everywhere

Climate

Mild & Rainy

10-20°C average, pack layers

Safety (Numbeo Safety Index)

Very Safe

Exeter is one of UK's safest cities

Frequently Asked Questions

Common questions about Master of Science in Pharmaceutical Quality Assurance & Regulation at Technological University Dublin

Can I work while studying?

International students can work up to 20 hours per week during term time and 40 hours per week during breaks. No separate work permit is needed, but full-time study in a one-year program is required.

What English language score do I need for this course?

Applicants need to meet specific English test requirements: Duolingo (overall 120), TOEFL (overall 80), IELTS (overall 6), or PTE (overall 65). Make sure to check individual section scores for each test.

What jobs can I get after studying this course?

Job titles for graduates include Quality Assurance Manager, Regulatory Affairs Specialist, Compliance Officer, Auditing Manager, and Manufacturing Supervisor.

What will I actually study in this course?

This course serves as a bridge for graduates in science or related fields, focusing on quality assurance and auditing within the pharmaceutical sector. It provides a comprehensive curriculum related to pharma and biopharmaceutical manufacturing.

When can I start — what are the intake months?

The intake month for the Master of Science in Pharmaceutical Quality Assurance & Regulation is September each year.
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