The LICQual Level 6 Diploma in Pharmaceutical Technology and Quality Assurance (D Pharmaceutical Technology) is an advanced qualification specifically designed for professionals seeking to enhance their career prospects, expand their expertise, and strengthen their Continuing Professional Development (CPD) within the pharmaceutical industry. This diploma is not intended for fresh candidates; instead, it is aimed at learners who already possess foundational knowledge or experience in pharmaceutical sciences, production, or quality assurance and wish to progress to higher levels of professional competence.
This programme provides learners with a comprehensive understanding of pharmaceutical manufacturing processes, quality control, regulatory compliance, and the principles of good manufacturing practice (GMP). Participants will develop the knowledge and skills required to manage pharmaceutical operations, ensure product safety and efficacy, and implement robust quality assurance systems across diverse pharmaceutical environments. The course also emphasizes the integration of technology and innovation in pharmaceutical production, enabling learners to optimize processes and contribute to organizational excellence.
Centres delivering the Level 6 Diploma in Pharmaceutical Technology and Quality Assurance must maintain high standards to ensure learner success. This includes employing competent and qualified staff with extensive experience in pharmaceutical technology and quality management. Centres are required to provide learners with access to up-to-date study materials, digital platforms, laboratory facilities, and practical tools to support both theoretical and applied learning.
By completing this qualification, learners will acquire the advanced technical knowledge, analytical skills, and professional competencies necessary to lead quality assurance initiatives, manage pharmaceutical production, and ensure compliance with industry standards, positioning themselves as highly skilled professionals within the pharmaceutical sector.
Course Overview
Qualification Title
LICQual Level 6 Diploma in Pharmaceutical Technology and Quality Assurance (D Pharmaceutical Technology)
Total Units
6
Total Credits
120
GLH
480
Qualification #
LICQ2201219
Qualification Specification
To enroll in the LICQual Level 6 Diploma in Pharmaceutical Technology and Quality Assurance (D Pharmaceutical Technology), applicants must meet the following criteria:
|
Qualification# |
Unit Title |
Credits |
GLH |
|---|---|---|---|
|
LICQ2201219-1 |
Principles of Pharmaceutical Technology |
20 |
80 |
|
LICQ2201219-2 |
Good Manufacturing Practice (GMP) and Regulatory Compliance |
20 |
80 |
|
LICQ2201219-3 |
Quality Assurance and Quality Control |
20 |
80 |
|
LICQ2201219-4 |
Pharmaceutical Process Optimization and Innovation |
20 |
80 |
|
LICQ2201219-5 |
Laboratory Techniques and Analytical Methods |
20 |
80 |
|
LICQ2201219-6 |
Research, Development, and Continuing Professional Development (CPD) |
20 |
80 |
By the end of this course, learners will be able to:
Unit 1: Principles of Pharmaceutical Technology
By the end of this unit, learners will be able to:
- Analyse the fundamentals of pharmaceutical production and technology
- Explain the stages of drug development, formulation, and manufacturing processes
- Evaluate the role of pharmaceutical technology in ensuring product safety and efficacy
Unit 2: Good Manufacturing Practice (GMP) and Regulatory Compliance
By the end of this unit, learners will be able to:
- Apply the principles of Good Manufacturing Practice (GMP) in pharmaceutical production
- Interpret regulatory frameworks and compliance requirements for international markets
- Implement documentation, auditing, and quality management systems to maintain standards
Unit 3: Quality Assurance and Quality Control
By the end of this unit, learners will be able to:
- Demonstrate knowledge of quality assurance and quality control practices in pharmaceutical operations
- Apply techniques for monitoring, testing, and validating pharmaceutical products
- Conduct risk assessments and implement corrective actions to ensure regulatory compliance
Unit 4: Pharmaceutical Process Optimisation and Innovation
By the end of this unit, learners will be able to:
- Analyse pharmaceutical production processes to identify areas for optimisation
- Apply innovative techniques and technological solutions to enhance manufacturing efficiency
- Integrate automation and advanced methods to improve product quality and workflow
Unit 5: Laboratory Techniques and Analytical Methods
By the end of this unit, learners will be able to:
- Perform advanced laboratory practices for pharmaceutical testing and analysis
- Utilise analytical instruments and validated methods for quality assessment
- Interpret laboratory data to support quality assurance and regulatory compliance
Unit 6: Research, Development, and Continuing Professional Development (CPD)
By the end of this unit, learners will be able to:
- Conduct research to support innovation and quality improvement in pharmaceutical technology
- Apply evidence-based practices to enhance operational efficiency and product quality
- Engage in CPD to maintain and advance professional knowledge, skills, and competencies
The LICQual Level 6 Diploma in Pharmaceutical Technology and Quality Assurance is designed for professionals seeking to develop advanced expertise in pharmaceutical production, quality assurance, and regulatory compliance. This qualification is ideal for learners who wish to enhance their career prospects, strengthen their Continuing Professional Development (CPD), and acquire the technical and managerial skills necessary to excel in the pharmaceutical sector.
This course is particularly suitable for:
- Pharmacists, pharmaceutical scientists, and laboratory professionals aiming to specialise in pharmaceutical technology and quality assurance
- Production managers and quality control officers seeking to improve manufacturing processes and ensure compliance with GMP standards
- Academics and trainers involved in pharmaceutical education and professional development
- Professionals working in regulatory affairs, research and development, or quality management within the pharmaceutical industry
- CPD-focused learners committed to advancing their knowledge, skills, and leadership capabilities in pharmaceutical operations
By enrolling in this diploma, learners will gain the expertise required to manage pharmaceutical production processes effectively, implement quality assurance systems, ensure compliance with industry regulations, and drive innovation in their organizations. The programme equips learners with the professional competencies to become highly skilled and influential contributors in the pharmaceutical sector.
Centres delivering the LICQual Level 6 Diploma in Pharmaceutical Technology and Quality Assurance must adhere to stringent standards to ensure learners receive a high-quality, professional, and engaging learning experience. These requirements guarantee that learners acquire the advanced knowledge, practical skills, and professional competencies essential for success in pharmaceutical technology and quality assurance.
- Qualified and Experienced Staff – Tutors, trainers, and assessors must hold relevant academic qualifications and professional experience in pharmaceutical technology, quality assurance, or related fields. Staff should actively engage in Continuing Professional Development (CPD) to remain current with industry standards, technological advancements, and regulatory requirements.
- Access to Learning and Training Resources – Centres must provide learners with up-to-date study materials, digital learning platforms, case studies, and practical tools to support both theoretical and applied learning.
- Specialised Facilities – Centres should maintain laboratories, simulation environments, and production facilities necessary for practical training, pharmaceutical testing, and quality assurance exercises.
- Robust Quality Assurance Systems – Centres must implement internal quality assurance processes, including learner progress monitoring, assessment verification, and compliance with LICQual standards.
- Comprehensive Learner Support – Learners should have access to academic guidance, mentoring, and professional support to enhance knowledge, practical competencies, and CPD outcomes.
- Commitment to Educational Excellence – Centres must uphold high standards of teaching, assessment, and learner engagement to ensure learners develop the technical, analytical, and professional skills required to excel in pharmaceutical production, quality management, and regulatory compliance.
By meeting these requirements, centres provide a world-class learning environment, equipping learners to become highly skilled professionals capable of contributing effectively to the pharmaceutical industry and advancing their careers.
Assessment and Verification
All units within this qualification are subject to internal assessment by the approved centre and external verification by LICQual. The qualification follows a criterion-referenced assessment approach, ensuring that learners meet all specified learning outcomes.
To achieve a ‘Pass’ in any unit, learners must provide valid, sufficient, and authentic evidence demonstrating their attainment of all learning outcomes and compliance with the prescribed assessment criteria. The Assessor is responsible for evaluating the evidence and determining whether the learner has successfully met the required standards.
Assessors must maintain a clear and comprehensive audit trail, documenting the basis for their assessment decisions to ensure transparency, consistency, and compliance with quality assurance requirements.
