The ICTQual AB Level 3 Diploma in Quality Control – Pharmaceutical is a comprehensive qualification designed to equip learners with the essential skills and technical knowledge required to ensure quality, compliance, and safety in pharmaceutical manufacturing and laboratory operations. This diploma offers in-depth coverage of quality control principles, testing procedures, and regulatory standards critical to producing safe and effective pharmaceutical products.
Learners will explore key areas such as Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), contamination control, raw material inspection, in-process and final product testing, as well as documentation and record-keeping in line with global pharmaceutical regulations like WHO, FDA, and EMA guidelines. The program also introduces risk management concepts, deviation handling, and quality audit processes used in pharmaceutical quality systems.
Whether you are new to the pharmaceutical industry or already working in a related role and seeking formal recognition of your skills, this diploma is ideal for building a strong foundation in quality assurance. It prepares learners for entry-level or supervisory positions in quality control labs, manufacturing plants, or regulatory departments—making it a valuable credential for those committed to maintaining the highest standards in medicine production and public health safety.
ICTQual AB Level 3 Diploma in Quality Control Pharmaceutical
This qualification, the ICTQual AB Level 3 Diploma in Quality Control Pharmaceutical, consists of 6 mandatory units.
- Fundamentals of Pharmaceutical Quality Control
- Introduction to Good Manufacturing Practices (GMP)
- Pharmaceutical Sampling and Analytical Techniques
- Documentation and Record-Keeping in Pharmaceutical Quality
- Deviation, Non-Conformance, and CAPA Management
- Internal Audits and Compliance Monitoring
Learning Outcomes for the Study Units:
1. Fundamentals of Pharmaceutical Quality Control – Learning Outcomes
By the end of this unit, learners will be able to:
- Understand the principles and objectives of pharmaceutical quality control
- Identify the key components of a pharmaceutical quality system
- Explain the importance of quality control in ensuring product safety and efficacy
- Distinguish between quality control and quality assurance functions
- Recognize the role of QC in regulatory compliance and risk mitigation
2. Introduction to Good Manufacturing Practices (GMP) – Learning Outcomes
By the end of this unit, learners will be able to:
- Define Good Manufacturing Practices and their significance in the pharmaceutical industry
- Interpret key GMP guidelines and regulatory requirements
- Apply basic GMP principles to daily operations in pharmaceutical settings
- Understand the responsibilities of personnel under GMP regulations
- Identify and implement GMP procedures in production and quality environments
3. Pharmaceutical Sampling and Analytical Techniques – Learning Outcomes
By the end of this unit, learners will be able to:
- Explain the purpose and importance of sampling in pharmaceutical quality control
- Identify appropriate sampling methods for raw materials, in-process, and finished products
- Conduct accurate sampling in compliance with standard operating procedures (SOPs)
- Apply basic analytical techniques for pharmaceutical testing
- Record and report test results with accuracy and integrity
4. Documentation and Record-Keeping in Pharmaceutical Quality – Learning Outcomes
By the end of this unit, learners will be able to:
- Understand the importance of documentation in a regulated pharmaceutical environment
- Maintain accurate and compliant records for quality-related activities
- Follow Good Documentation Practices (GDP) in creating and reviewing records
- Identify different types of documents used in QC and GMP systems
- Ensure traceability and accountability through proper documentation procedures
5. Deviation, Non-Conformance, and CAPA Management – Learning Outcomes
By the end of this unit, learners will be able to:
- Define deviations and non-conformances within the quality control process
- Understand the root cause analysis process and its application in quality systems
- Implement Corrective and Preventive Actions (CAPA) to address quality issues
- Document deviations and CAPA actions in compliance with regulatory standards
- Monitor the effectiveness of CAPA and continuous improvement initiatives
6. Internal Audits and Compliance Monitoring – Learning Outcomes
By the end of this unit, learners will be able to:
- Understand the purpose and process of internal audits in pharmaceutical quality systems
- Participate in audit planning, execution, and follow-up activities
- Identify non-compliance issues and suggest appropriate corrective measures
- Evaluate organizational compliance with GMP and standard operating procedures
- Contribute to audit readiness and regulatory inspection preparedness
Benefits of the ICTQual AB Level 3 Diploma in Quality Control Pharmaceutical
Comprehensive Industry Knowledge
Gain a deeper understanding of pharmaceutical quality control systems, including GMP, SOPs, quality audits, and regulatory frameworks such as FDA, WHO, and EMA standards.
Practical Skill Development
Learn hands-on techniques for sampling, product testing, contamination control, documentation, and deviation reporting—skills highly valued in pharmaceutical production and quality assurance roles.
Improved Career Prospects
This diploma enhances your employability in a variety of pharmaceutical settings, including quality control labs, production units, R&D departments, and regulatory compliance offices.
Qualification for Entry- and Mid-Level Roles
Equip yourself for positions such as Quality Control Technician, Lab Assistant, QA Associate, or Production Supervisor within the pharmaceutical and biotech industries.
Compliance and Risk Management Skills
Understand how to identify and minimize quality-related risks, follow documentation protocols, and ensure compliance with international pharmaceutical regulations.
Foundation for Advanced Learning
Acts as a stepping stone to higher-level qualifications, such as Level 4 or Level 5 Diplomas in Pharmaceutical Science, Quality Management, or Regulatory Affairs.
Industry-Relevant and Recognized Qualification
Earn an internationally recognized certification that validates your capabilities and commitment to high-quality pharmaceutical standards.
Applicable to Related Sectors
The knowledge and skills gained in this course are transferable to related sectors like biotechnology, medical device manufacturing, cosmetics, and nutraceuticals.
Enhanced Professional Confidence
Build the confidence to operate in highly regulated environments where attention to detail, precision, and compliance are essential.
Support for Public Health and Safety
Contribute meaningfully to the development and distribution of safe, effective medicines, playing a vital role in maintaining public trust in healthcare products.
Who is the ICTQual AB Level 3 Diploma in Quality Control Pharmaceutical Best Suited For?
The ICTQual AB Level 3 Diploma in Quality Control – Pharmaceutical is tailored for individuals who aspire to work in the highly regulated and scientifically driven pharmaceutical industry, particularly in roles focused on quality, compliance, and product safety. The ideal learner for this course includes:
Aspiring Pharmaceutical Professionals
Individuals seeking to start a career in the pharmaceutical sector, especially in areas such as quality control, manufacturing, laboratory analysis, or regulatory compliance.
Science and Health Graduates
Recent school or college graduates with backgrounds in biology, chemistry, biotechnology, or health sciences who want to pursue a career in the pharmaceutical industry.
Entry-Level Workers in Pharmaceutical or Healthcare Manufacturing
Those currently employed in pharmaceutical production or quality-related roles who wish to enhance their qualifications, knowledge, and promotion prospects.
Career Switchers
Professionals from related industries like food production, cosmetics, biotechnology, or healthcare who want to transition into pharmaceutical quality control roles with the necessary technical and regulatory knowledge.
Individuals Interested in Compliance and Safety
Learners with strong attention to detail and an interest in quality, safety standards, and process improvement who want to ensure products meet strict regulatory and safety guidelines.
Future Quality Control or Assurance Specialists
Those aiming to progress into more advanced quality roles or leadership positions in the pharmaceutical field by building a solid foundation in GMP, SOPs, and global compliance systems.
This course is ideal for detail-oriented, science-minded individuals who value precision, regulatory responsibility, and the critical role of quality in protecting patient health and pharmaceutical product integrity.
Entry Requirements
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Qualification Process
Qualification Process for the ICTQual AB Level 3 Diploma in Quality Control Pharmaceutical
- Self-Assessment:
Begin by evaluating your eligibility to ensure you meet the qualification requirements, including work experience, knowledge, and language proficiency. - Registration:
Complete your registration by submitting the required documents, including a scanned copy of a valid ID, and paying the registration fee. - Induction:
An assessor will conduct an induction to confirm your eligibility for the course and explain the evidence requirements. If you do not meet the criteria, your registration will be cancelled, and the fee will be refunded. - Assignments & Evidence Submission:
Provide all assignments and the necessary evidence based on the assessment criteria outlined in the course. If you are unsure of the required evidence, consult with the assessor for guidance on the type and nature of evidence needed. - Feedback and Revision:
The assessor will review your submitted evidence and provide feedback. Evidence that meets the criteria will be marked as “Criteria Met,” while any gaps will be identified. You will be asked to revise and resubmit if needed. - Competence Evidence:
Submit final evidence demonstrating that all learning outcomes have been met. This evidence will be marked as “Criteria Met” by the assessor once it is satisfactory. - Internal Quality Assurance (IQA):
The Internal Quality Assurance Verifier (IQA) will review your evidence to ensure consistency, quality, and compliance with standards. - External Verification:
The IQA will submit your portfolio to ICTQUAL AB External Quality Assurance Verifiers (EQA) for final confirmation. The EQA may contact you directly to verify the authenticity of your evidence. - Certification:
Upon successful completion of all checks, ICTQUAL AB will issue your official certificate, confirming that you have attained the ICTQual AB Level 3 Diploma in Quality Control Pharmaceutical.
