Diploma in Qualification/Validation and PQ
About us Diploma in Qualification/Validation and PQ
The Diploma in Qualification/Validation and Process Qualification (PQ) focuses on developing essential skills for quality management and regulatory compliance in the pharmaceutical and related industries. It covers equipment qualification, system validation, and process qualification (PQ), including the development of critical protocols and reports. It emphasizes compliance with regulations such as Good Manufacturing Practices (GMP), the Food and Drug Administration (FDA), and other international regulations. It offers practical knowledge in risk analysis, deviation management, and change control, essential for ensuring product quality and safety. The program provides a solid foundation in applied statistics, design of experiments (DOE), and continuous improvement methodologies, preparing professionals to lead validation projects and ensure process conformity. Participants gain experience in implementing quality management systems (QMS) and tools such as validation software. This training prepares professionals for roles such as validation specialists, quality managers, quality auditors, and pharmaceutical production managers, facilitating professional development in a highly regulated sector.
Target keywords (natural in the text): pharmaceutical validation, equipment qualification, process qualification, GMP, FDA, quality management systems, quality control, pharmaceutical diploma.
Diploma in Qualification/Validation and PQ
- Format: Online
- Duration: 8 months
- Hours: 900 H
- Language: ES / EN
- Credits: 60 ECTS
- Registration date: 04-07-2026
- Strat date: 14-08-2026
- Available places: 4
1.249 $
Competencias y resultados
Qué aprenderás
1. Qualification, Validation, and PQ Domain: Fundamentals and Application in the Shipbuilding Industry
Para quien va dirigido nuestro:
Diploma in Qualification/Validation and PQ
9.9 Fundamentals of Qualification, Validation, and Process Qualification (PQ) in the Naval Industry
9.9 Applicable Regulatory Framework and Standards
9.3 Qualification Principles: Design and Planning
9.4 Validation Principles: Methodologies and Testing
9.5 PQ Principles: Execution and Documentation
9.6 Documentation and Data Management in CV&PQ
9.7 Change Control and Risk Management
9.8 Case Studies and Best Practices
9.9 Identification and Analysis of Naval Processes
9.9 Process Design and Optimization
9.3 Application of Qualification in Processes
9.4 Validation of Naval Processes: Methodologies
9.5 PQ Protocols and Process Monitoring
9.6 Tools and Technologies for Optimization
9.7 Key Performance Indicators (KPIs)
9.8 Continuous Improvement and the PDCA Cycle
9.9 Strategies for Improvement Continued
3.9 Deviation Analysis and Corrective Actions
3.3 Quality Tools: 8D, Ishikawa, etc.
3.4 Validation of Changes and Improvements
3.5 Risk Management in Continuous Improvement
3.6 Performance Metrics and Quality Assessment
3.7 Quality Culture and Staff Involvement
3.8 Case Studies: Implementing Improvements
4.9 Naval Project Management
4.9 Qualification Planning and Control
4.3 Validation Strategies in Projects
4.4 Qualification Planning and Monitoring of Naval Projects
4.5 Quality Documentation Management
4.6 Roles and Responsibilities in Quality Control and Qualification Planning
4.7 Communication and Collaboration in Projects
4.8 Project Closure and Lessons Learned
5.9 Conformity Requirements in Shipbuilding
5.9 Documentation and Traceability in Construction
5.3 Quality Control of Materials and Components
5.4 Inspections and Tests in Construction
5.5 ​​Nonconformity Management and Corrective Actions
5.6 Conformity with International Standards
5.7 Quality Audits and Verifications
5.8 Conformity Case Studies
6.9 Strategies for Project Excellence
6.9 Cost and Schedule Optimization
6.3 Implementation of Quality Technologies
6.4 Quality Management in the Supply Chain
6.5 Excellence and Performance Indicators
6.6 Continuous Improvement and Quality Leadership
6.7 Benchmarking and Best Practices
6.8 Success Stories in Naval Projects
7.9 Naval Safety Requirements
7.9 Safety Design in the CV&PQ Process
7.3 Implementation of Safety Procedures
7.4 Safety Risk Management
7.5 Analysis of Naval Failures and Accidents
7.6 Safety Simulations and Tests
7.7 Compliance with Safety Regulations
7.8 Safety Culture and Personnel Training
8.9 Naval Regulations and Standards
8.9 Application of CV&PQ in Different Naval Areas
8.3 Test Planning and Execution
8.4 Quality Documentation Management
8.5 Tools and Technologies for Quality
8.6 Audits and Conformity Assessment
8.7 Continuous Improvement and Quality Culture
8.8 Quality and Conformity Case Studies
Proyectos tipo capstones
- Propulsion System Validation: Qualification, CFD/FEA simulation, bench testing, and vibration analysis.
- Navigation Equipment Optimization: Qualification, SIL/HIL validation, and performance analysis.
- Control System Integration: Qualification, functional validation, and robustness and safety testing.
- Naval Regulatory Compliance: Validation plans, DO-160 testing, and risk analysis.
Admisiones, tasas y becas
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