LICQual Level 3 Certificate in Pharmaceutical Technology and Quality Assurance (Cert Pharmaceutical Technology)

The LICQual Level 3 Certificate in Pharmaceutical Technology and Quality Assurance (Cert Pharmaceutical Technology) is a specialized qualification designed for professionals in the pharmaceutical and healthcare industries who wish to advance their expertise in pharmaceutical manufacturing, technology, and quality assurance processes. This course is not intended for fresh entrants; it is tailored for experienced professionals seeking to enhance their career prospects, broaden their knowledge, and actively engage in Continuing Professional Development (CPD).

Learners undertaking this programme will gain comprehensive knowledge of pharmaceutical technology, including formulation, manufacturing techniques, and quality control measures. The course emphasises the application of industry best practices, regulatory compliance, and quality assurance principles to ensure that pharmaceutical products are safe, effective, and of high quality. Practical skills, critical thinking, and adherence to international standards are key components of the programme, enabling learners to contribute effectively to pharmaceutical operations and regulatory processes.

LICQual ensures that centres delivering this qualification maintain the highest standards of training. Centres must employ competent and qualified staff, provide up-to-date learning materials, and maintain suitable facilities and resources to support effective teaching and learner success. This guarantees that learners receive structured guidance, practical exposure, and the expertise necessary to excel in pharmaceutical technology and quality assurance roles.

By completing the Level 3 Certificate in Pharmaceutical Technology and Quality Assurance, learners demonstrate their commitment to professional growth and excellence in pharmaceutical practice. This course is ideal for pharmacy technicians, quality assurance officers, manufacturing professionals, and other healthcare practitioners who wish to specialize in pharmaceutical technology, improve operational efficiency, and strengthen their professional competence in the industry.

Course Overview


Qualification Title

LICQual Level 3 Certificate in Pharmaceutical Technology and Quality Assurance (Cert Pharmaceutical Technology)

Total Units

6

Total Credits

60

GLH

240

Qualification #

LICQ2201154


Qualification Specification

Download Qualification Specification

To enroll in the LICQual Level 3 Certificate in Pharmaceutical Technology and Quality Assurance (Cert Pharmaceutical Technology), applicants must meet the following criteria:

  • Age Requirement: Applicants must be at least 18 years old.
  • Educational Requirements: Learners should hold a relevant pharmacy, pharmaceutical science, or healthcare qualification at Level 2 or equivalent to provide a solid foundation for advanced pharmaceutical technology studies.
  • Experience: Practical experience in pharmaceutical manufacturing, quality assurance, laboratory work, or related professional roles is essential. This course is designed for experienced professionals rather than fresh entrants.
  • English Language Proficiency: Applicants must have a good command of the English language. Non-native English speakers should demonstrate English proficiency equivalent to IELTS 5.0 or CEFR Level B1 to ensure effective participation and comprehension.
  • Commitment to CPD: Learners must show a commitment to Continuing Professional Development (CPD), actively applying newly acquired knowledge and skills in professional practice.
  • Access to Required Resources: Learners must have access to appropriate learning tools, reference materials, and practical resources necessary for study and application. Centres delivering this qualification provide comprehensive materials and facilities to support learner success.

Qualification#

Unit Title

Credits

GLH

LICQ2201154-1

Principles of Pharmaceutical Technology

10

40

LICQ2201154-2

Pharmaceutical Quality Assurance and Control

10

40

LICQ2201154-3

Pharmaceutical Manufacturing Processes

10

40

LICQ2201154-4

Regulatory Compliance and Pharmaceutical Legislation

10

40

LICQ2201154-5

Laboratory Techniques and Analytical Methods

10

40

LICQ2201154-6

Risk Management and Continuous Improvement in Pharmaceutical Practice

10

40

By the end of this course, learners will be able to:

  1. Principles of Pharmaceutical Technology
    • Explain key principles and applications of pharmaceutical technology in healthcare
    • Describe formulation science and drug delivery systems for various pharmaceutical products
    • Analyse pharmaceutical manufacturing processes and associated equipment
  2. Pharmaceutical Quality Assurance and Control
    • Apply quality assurance (QA) and quality control (QC) principles in pharmaceutical production
    • Implement Good Manufacturing Practices (GMP) to ensure compliance and product safety
    • Conduct inspections, audits, and quality assessments to maintain high standards
  3. Pharmaceutical Manufacturing Processes
    • Demonstrate understanding of batch and continuous manufacturing techniques
    • Operate and optimise production workflows and equipment effectively
    • Identify critical control points and apply troubleshooting strategies to manufacturing challenges
  4. Regulatory Compliance and Pharmaceutical Legislation
    • Interpret national and international pharmaceutical regulations relevant to practice
    • Apply ethical and legal standards in pharmaceutical operations
    • Maintain accurate documentation and records to meet regulatory requirements
  5. Laboratory Techniques and Analytical Methods
    • Conduct laboratory testing and analysis of pharmaceutical products
    • Apply analytical methods to assess drug purity, potency, and stability
    • Use laboratory results to support quality assurance and continuous improvement initiatives
  6. Risk Management and Continuous Improvement in Pharmaceutical Practice
    • Identify, assess, and mitigate risks in pharmaceutical manufacturing and QA processes
    • Implement strategies for continuous improvement to enhance quality and efficiency
    • Monitor and evaluate performance to ensure safe, effective, and high-quality pharmaceutical outcomes

The LICQual Level 3 Certificate in Pharmaceutical Technology and Quality Assurance is specifically designed for professionals in the pharmaceutical and healthcare industries who wish to develop specialised skills in manufacturing, quality assurance, and regulatory compliance. This course is ideal for:

  • Pharmacy Technicians and Pharmaceutical Assistants seeking to advance their expertise in pharmaceutical technology
  • Quality Assurance and Quality Control Officers aiming to enhance their knowledge of compliance and product standards
  • Manufacturing and Production Professionals looking to optimise workflow and operational efficiency in pharmaceutical settings
  • Laboratory and Analytical Staff responsible for testing and evaluating pharmaceutical products
  • Healthcare Professionals wishing to specialise in pharmaceutical manufacturing and quality assurance
  • Experienced Professionals looking to enhance their CPD portfolio and career prospects in the pharmaceutical industry

This course is not intended for fresh entrants; it is tailored for learners with prior professional experience or relevant educational backgrounds. By enrolling, learners will gain the practical skills, theoretical knowledge, and professional competencies required to excel in pharmaceutical technology and quality assurance roles, ensuring safe, effective, and high-quality outcomes.

To deliver the LICQual Level 3 Certificate in Pharmaceutical Technology and Quality Assurance effectively and ensure high-quality learner outcomes, centres must meet the following requirements:

  • Qualified and Competent Staff: Tutors and assessors must hold relevant qualifications in pharmacy, pharmaceutical science, or quality assurance, with proven experience in pharmaceutical manufacturing and professional practice.
  • Comprehensive Learning Resources: Centres must provide up-to-date textbooks, reference materials, laboratory equipment, digital tools, and practical resources to support theoretical and practical learning.
  • Appropriate Facilities: Classrooms, laboratories, and production simulation areas must be equipped to deliver both theoretical instruction and hands-on practical activities.
  • Assessment and Evaluation Systems: Centres should implement robust assessment methods, including assignments, practical exercises, case studies, and examinations aligned with international standards.
  • Support for Continuing Professional Development (CPD): Centres must encourage learners to engage in CPD activities, applying newly acquired skills and knowledge in professional pharmaceutical practice.
  • Health and Safety Compliance: All practical sessions and laboratory work must adhere to relevant health and safety protocols to protect learners, staff, and the working environment.

By meeting these centre requirements, institutions ensure learners receive structured guidance, high-quality resources, and practical support necessary to successfully complete the qualification and excel in pharmaceutical technology and quality assurance roles.

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.

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