Description
Advanced Pharmaceutical Quality Control (QC) & Quality Assurance (QA) Training
Boost your pharma career with this Advanced Pharmaceutical QC & QA Training that meets global industry standards. This course covers cGMP regulations, ICH guidelines (Q1–Q10), analytical method validation (HPLC, UV), documentation (SOPs, MBR/BMR), sterile manufacturing, and quality risk management.
Learn to implement Quality Management Systems (QMS), handle audits, ensure data integrity, and manage laboratory operations with real-world, job-ready skills.
Key Highlights
- ICH Guidelines (Q1–Q10): Stability, validation, impurities, GMP & QMS
- Analytical Techniques: HPLC, GC, UV-Vis, IR, Dissolution
- Method Validation: Accuracy, precision, linearity, LOD, LOQ
- Documentation: SOPs, MBR, BMR, change control, data integrity
- Manufacturing & Validation: Process validation, VMP, IPQC
- Sterile Products: Aseptic processing, sterilisation, environmental control
- Quality Risk Management: Q9, FMEA tools
- Audit Readiness: Internal audits, FDA inspections, CAPA, recalls
Core Modules
- Quality Assurance (QA) & Total Quality Management (TQM)
- Quality Control (QC) & GLP Laboratory Practices
- Regulatory Affairs (DMF, CTD, eCTD)
- Validation & Calibration
- Audits, Deviations, Complaints & Recalls
Who Should Enroll?
- BSc, MSc, B.Pharm, M.Pharm graduates
- QA/QC professionals and lab analysts
- Freshers aiming for pharma industry roles
Career Opportunities
QC Analyst | QA Executive | Validation Officer | Regulatory Affairs Associate | Production Quality Specialist
Bonus
Includes interview preparation, real-world case studies, and frequently asked pharma interview questions to help you get hired faster.
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