Pharma Tech & Quality Assurance Diploma | LICQual L3
Modern healthcare relies on medicines that are not only effective but also safe, consistent, and reliable. Behind every tablet, capsule, or injectable lies a complex process of design, testing, and monitoring that ensures patients receive treatments of the highest standard. This is where pharmaceutical technology and quality assurance play a critical role. They form the backbone of drug development and manufacturing, combining innovation with rigorous safety checks to protect public health.
The LICQual Level 3 Diploma in Pharmaceutical Technology and Quality Assurance (Dip Pharmaceutical Technology) highlights the growing importance of this discipline in today’s pharmaceutical industry. Pharmaceutical technology and quality assurance are not simply about compliance—they are about building trust, advancing science, and ensuring that medicines meet international standards. As new therapies, biologics, and advanced formulations emerge, professionals trained in this field are essential for bridging innovation with patient safety. For learners, engaging with this subject is more than academic—it is an opportunity to contribute to global healthcare, strengthen industry practices, and play a pivotal role in shaping the future of medicine.
Program Outline
The LICQual Level 3 Diploma in Pharmaceutical Technology and Quality Assurance (Dip Pharmaceutical Technology) is a structured qualification designed to provide learners with essential knowledge of drug development and manufacturing standards. Comprising 6 specialized units and worth 60 credits, the program introduces learners to areas such as formulation science, process validation, compliance frameworks, risk management, regulatory standards, and ethical considerations in pharmaceutical technology and quality assurance.
This section explains how the course equips learners with the ability to understand pharmaceutical technology and quality assurance, apply evidence‑based approaches, and align with international standards effectively. It highlights the type of learners the program is aimed at, the skills they will gain, and the career pathways available upon completion. Readers will also discover how this internationally recognized qualification opens opportunities in hospitals, pharmaceutical companies, biotechnology firms, and research institutions, making it a valuable credential for anyone aspiring to build a career in pharmaceutical technology and quality assurance..
Unit Structure
| Qualification | Unit Title | Credits | GLH |
| LICQ2201187-1 | Principles of Pharmaceutical Technology | 10 | 40 |
| LICQ2201187-2 | Pharmaceutical Formulation and Dosage Design | 10 | 40 |
| LICQ2201187-3 | Manufacturing Processes in the Pharmaceutical Industry | 10 | 40 |
| LICQ2201187-4 | Quality Assurance and Quality Control in Pharmaceuticals | 10 | 40 |
| LICQ2201187-5 | Regulatory Frameworks, Compliance, and Good Manufacturing Practice (GMP) | 10 | 40 |
| LICQ2201187-6 | Research, Innovation, and Professional Development in Pharmaceutical Technology | 10 | 40 |
Who Can Benefit
The LICQual Level 3 Diploma in Pharmaceutical Technology and Quality Assurance (Dip Pharmaceutical Technology) is designed for individuals who want to specialize in drug development, manufacturing, and compliance. This program is particularly valuable for those who aim to address challenges such as product safety, regulatory alignment, and process efficiency. It helps learners strengthen their expertise, improve employability, and prepare for roles where pharmaceutical technology and quality assurance are central to healthcare delivery.
Ideal Learners
- Students aspiring to enter pharmaceutical sciences with a focus on technology and quality assurance.
- Entry‑level professionals seeking structured training in pharmaceutical technology and quality assurance.
- Pharmacy assistants wanting to expand knowledge of compliance and manufacturing standards.
- Community pharmacy staff preparing for responsibilities in product safety.
- Hospital pharmacy technicians aiming to strengthen skills in quality assurance practices.
- Healthcare professionals transitioning into pharmaceutical technology and quality assurance roles.
- Career changers interested in pharmaceutical manufacturing and regulatory compliance.
- Ambitious learners who want to develop practical skills for pharmaceutical technology and quality assurance careers.
What You’ll Be Able to Do
Unit 1: Principles of Pharmaceutical Technology
By the end of this unit, learners will be able to:
- Explain the fundamental concepts of pharmaceutical technology and its role in healthcare.
- Describe the properties of pharmaceutical raw materials and their applications.
- Analyse the principles of drug development, including solubility, stability, and bioavailability.
- Apply core scientific principles to the design and evaluation of pharmaceutical processes.
Unit 2: Pharmaceutical Formulation and Dosage Design
By the end of this unit, learners will be able to:
- Demonstrate knowledge of dosage forms, excipients, and formulation strategies.
- Evaluate the stability and compatibility of pharmaceutical ingredients in formulation.
- Apply principles of dosage design to ensure therapeutic efficacy and patient safety.
- Assess bioavailability and pharmacokinetics in relation to dosage form design.
Unit 3: Manufacturing Processes in the Pharmaceutical Industry
By the end of this unit, learners will be able to:
- Identify key pharmaceutical manufacturing processes including granulation, compression, and encapsulation.
- Explain the principles of sterile and non-sterile production methods.
- Apply process validation and scale-up principles in pharmaceutical manufacturing.
- Evaluate safety, efficiency, and quality considerations in production environments.
Unit 4: Quality Assurance and Quality Control in Pharmaceuticals
By the end of this unit, learners will be able to:
- Explain the role of quality assurance (QA) and quality control (QC) in pharmaceutical production.
- Apply analytical and testing methods to assess product quality.
- Evaluate documentation systems, audits, and inspections in QA frameworks.
- Demonstrate knowledge of validation, calibration, and risk management procedures.
Unit 5: Regulatory Frameworks, Compliance, and Good Manufacturing Practice (GMP)
By the end of this unit, learners will be able to:
- Explain international regulatory frameworks governing pharmaceutical production.
- Analyse compliance requirements under GMP and related quality standards.
- Demonstrate knowledge of ethical, legal, and professional responsibilities in pharmaceutical practice.
- Apply GMP principles to ensure safe and compliant manufacturing processes.
Unit 6: Research, Innovation, and Professional Development in Pharmaceutical Technology
By the end of this unit, learners will be able to:
- Conduct research using appropriate methods relevant to pharmaceutical technology.
- Critically evaluate data and apply evidence-based decision-making in practice.
- Demonstrate innovation in problem-solving within pharmaceutical product development.
- Reflect on professional development needs and plan for Continuing Professional Development (CPD).
