The LICQual Level 7 Postgraduate Diploma in Pharmaceutical Technology and Quality Assurance (PgD Level 7 Pharmaceutical Technology) is a specialized qualification designed for experienced pharmacy and pharmaceutical industry professionals who wish to advance their expertise in pharmaceutical technology, manufacturing processes, and quality assurance. This advanced programme is ideal for learners seeking to enhance their career prospects, broaden their technical knowledge, and actively engage in Continuing Professional Development (CPD). It provides an in-depth understanding of drug formulation, manufacturing standards, regulatory compliance, and quality management systems within the pharmaceutical sector.
This postgraduate diploma is particularly suitable for pharmacists, pharmaceutical scientists, quality assurance specialists, and professionals involved in drug development and production. Learners will acquire the skills to ensure compliance with regulatory frameworks, implement best practices in quality assurance, optimise manufacturing processes, and contribute to the delivery of high-quality pharmaceutical products.
LICQual ensures that centres delivering this Level 7 qualification maintain the highest standards of education. Centres must employ competent and qualified staff with extensive experience in pharmaceutical technology, quality assurance, and regulatory compliance, and provide learners with access to essential materials, laboratory facilities, and digital resources. This guarantees a rigorous, supportive, and engaging learning environment that promotes learner success, professional growth, and practical application of knowledge.
By completing this diploma, learners will achieve a prestigious Level 7 qualification, positioning themselves as experts in pharmaceutical technology and quality assurance, and equipping them to make a meaningful impact on drug development, production, and regulatory compliance within the pharmaceutical industry.
Course Overview
Qualification Title
LICQual Level 7 Postgraduate Diploma in Pharmaceutical Technology and Quality Assurance (PgD Level 7 Pharmaceutical Technology)
Total Units
6
Total Credits
120
GLH
600
Qualification #
LICQ2201251
Qualification Specification
To enroll in the LICQual Level 7 Postgraduate Diploma in Pharmaceutical Technology and Quality Assurance (PgD Level 7 Pharmaceutical Technology), applicants must meet the following criteria:
Qualification# |
Unit Title 19519_08374e-54> |
Credits 19519_2b001f-31> |
GLH 19519_b3de4d-fe> |
---|---|---|---|
LICQ2201251-1 19519_b09f82-8c> |
Principles of Pharmaceutical Technology 19519_36f65d-08> |
20 19519_a12065-68> |
100 19519_4b41c5-ad> |
LICQ2201251-2 19519_963db0-18> |
Advanced Manufacturing Processes in Pharmaceuticals 19519_9ccafb-49> |
20 19519_ea765e-71> |
100 19519_ab5bcd-bc> |
LICQ2201251-3 19519_104641-19> |
Quality Assurance and Control in Pharmaceutical Practice 19519_8d097c-8f> |
20 19519_981876-32> |
100 19519_f8a77c-84> |
LICQ2201251-4 19519_0b250b-e1> |
Regulatory Affairs and Compliance in Pharmaceuticals 19519_22f71a-c2> |
20 19519_e423d1-33> |
100 19519_581b0d-74> |
LICQ2201251-5 19519_3da66f-bb> |
Research, Innovation, and Technology in Pharmaceutical Development 19519_e950ca-cf> |
20 19519_fc28f4-40> |
100 19519_78a571-b6> |
LICQ2201251-6 19519_bfc554-03> |
Leadership, Management, and Professional Development in Pharmaceuticals 19519_45cfbd-b0> |
20 19519_878ecb-c6> |
100 19519_99f0cc-d7> |
By the end of this course, learners will be able to:
Unit 1: Principles of Pharmaceutical Technology
Learners will be able to
- Critically analyse the fundamentals of drug formulation, dosage forms, and delivery systems
- Apply knowledge of pharmaceutical materials and excipients to optimise formulations
- Evaluate strategies for developing and improving pharmaceutical products
- Develop solutions to enhance the stability, efficacy, and safety of medicines
Unit 2: Advanced Manufacturing Processes in Pharmaceuticals
Learners will be able to
- Analyse modern manufacturing techniques and process optimisation strategies
- Apply Good Manufacturing Practices (GMP) in pharmaceutical production
- Evaluate production workflows to improve efficiency, quality, and compliance
- Implement strategies for scaling up laboratory formulations to industrial production
Unit 3: Quality Assurance and Control in Pharmaceutical Practice
Learners will be able to
- Design and implement robust quality management systems for pharmaceutical products
- Apply quality control testing methods to ensure product safety and efficacy
- Evaluate risk management and validation processes in manufacturing environments
- Develop continuous improvement strategies to enhance QA/QC procedures
Unit 4: Regulatory Affairs and Compliance in Pharmaceuticals
Learners will be able to
- Interpret global regulatory frameworks and industry standards for pharmaceuticals
- Apply compliance strategies to meet legal, ethical, and safety requirements
- Evaluate documentation, audits, and licensing processes to ensure adherence
- Develop procedures to maintain regulatory compliance throughout the product lifecycle
Unit 5: Research, Innovation, and Technology in Pharmaceutical Development
Learners will be able to
- Plan, conduct, and evaluate research projects in pharmaceutical sciences
- Analyse data and interpret results to inform product development and innovation
- Apply emerging technologies to enhance pharmaceutical processes and product quality
- Integrate evidence-based research into practical pharmaceutical applications
Unit 6: Leadership, Management, and Professional Development in Pharmaceuticals
Learners will be able to
- Apply leadership principles and strategic decision-making in pharmaceutical settings
- Manage projects, teams, and resources effectively to achieve organisational objectives
- Evaluate ethical, professional, and operational challenges in the pharmaceutical industry
- Develop professional growth strategies and lead initiatives to enhance organisational performance
The LICQual Level 7 Postgraduate Diploma in Pharmaceutical Technology and Quality Assurance is designed for experienced professionals in the pharmaceutical industry who wish to advance their expertise in drug development, manufacturing, and quality management. This course is ideal for:
- Pharmacists and Pharmaceutical Scientists seeking to enhance their technical knowledge in formulation, production, and quality assurance
- Quality Assurance and Regulatory Professionals aiming to ensure compliance with global pharmaceutical standards and regulations
- Production and Manufacturing Specialists looking to optimise processes, implement Good Manufacturing Practices (GMP), and improve operational efficiency
- Researchers and Innovation Leaders wishing to contribute to the development of new pharmaceutical technologies and evidence-based practices
- Professionals Committed to CPD and lifelong learning, seeking a prestigious Level 7 qualification to advance their career and assume leadership roles in pharmaceutical organisations
This programme is suitable for learners with substantial experience in pharmaceutical science, manufacturing, or quality assurance who are motivated to apply advanced principles, enhance operational performance, and make a meaningful impact on product quality, regulatory compliance, and professional practice in the pharmaceutical sector.
Centres delivering the LICQual Level 7 Postgraduate Diploma in Pharmaceutical Technology and Quality Assurance must maintain the highest standards to ensure learners receive an exceptional and effective learning experience. To deliver this advanced programme successfully, centres are required to:
- Employ Competent and Qualified Staff: Tutors and facilitators must possess extensive experience and relevant qualifications in pharmaceutical technology, quality assurance, manufacturing, and regulatory compliance to provide expert guidance to learners
- Provide Access to Essential Learning Resources: Centres must ensure learners have access to up-to-date academic journals, laboratory facilities, pharmaceutical reference materials, and digital learning platforms necessary for completing research projects and assessments
- Maintain Suitable Learning Facilities: Classrooms, laboratories, and digital learning environments should be equipped with modern technology to support interactive teaching, practical training, and independent study
- Ensure Compliance with Ethical and Professional Standards: Centres must adhere to professional, legal, and ethical standards in pharmaceutical education and practice, including data protection, safety protocols, and quality assurance
- Support Learner Progress and Development: Centres should implement robust assessment, monitoring, and feedback systems to guide learners successfully through the programme and enhance professional competencies
- Encourage Continuing Professional Development (CPD): Centres should provide opportunities for learners to engage in workshops, seminars, and additional professional development activities to promote ongoing growth
By meeting these requirements, centres ensure that learners enrolled in the PgD Level 7 Pharmaceutical Technology programme receive a high-quality, comprehensive education that supports career advancement, professional development, and excellence in pharmaceutical technology and quality assurance practice.
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.