Course Link : https://www.sgpharmatrainings.com/courses/365956?utm_source%3Dother%26utm_medium%3Dtutor-course-referral%26utm_campaign%3Dcourse-overview-webapp

Are you looking to build a strong career in Pharmaceutical Quality Control (QC)?Do you want to learn industry-standard QC practices, analytical techniques, documentation, and lab skills exactly the way top pharma companies expect?

This comprehensive Certificate Course in Pharmaceutical Quality Control (QC) is designed for students, freshers, and working professionals who want to gain practical, job-ready knowledge in the QC domain.

With a curriculum aligned to FDA, WHO, ICH, and CDSCO expectations, this course gives you complete exposure to QC lab operations, analytical testing, regulatory standards, and compliance practices—making you industry-ready from Day 1.

What You Will Learn

Section 1: Fundamentals of Pharma QC

Core concepts of QC and its vital role in drug development

Overview of pharma departments & cross-functional responsibilities

Regulatory bodies: FDA, WHO, ICH, CDSCO

Dosage forms and pharmacopeial standards

Section 2: QC Laboratory Setup

Complete QC lab design, infrastructure & workflow

Lab safety, PPE, calibration, and equipment maintenance

Temperature, humidity & environmental monitoring

Handling hazardous chemicals & waste disposal

Section 3: QC Sections and Activities

Raw material, IPQC, intermediate & finished product testing

Stability studies and control sample management

Microbiology operations & QMS essentials

Good Laboratory Practices (GLP)

Section 4: Types of QC Testing

Sampling techniques and acceptance criteria

Chemical, physical, and microbiological testing methodologies

Section 5: Analytical Instruments & Techniques

Wet chemistry, titrations, UV, IR

HPLC, GC, dissolution profiling

Impurity analysis, residual solvents & instrument principles

Section 6: Microbiological Testing

Sterility testing & microbial limit tests

Environmental monitoring in micro labs

Endotoxin testing & media preparation/validation

Section 7: Documentation & Compliance

GLP, ALCOA+, SOPs, logbooks & data integrity

Audit readiness, CAPA, OOS handling

Deviations, incidents & change control

Section 8: Advanced QC Concepts

Advanced stability studies & protocols

Method validation, method transfer & reference standards

QC risk assessment and digital QC systems

LIMS & current trends like automation and CSV

Section 9: Operational Excellence & Career Growth

Introduction to Lean Six Sigma concepts

Communication skills & QC career pathways

Who Should Enroll?

This course is ideal for:

B Pharm, M Pharm, Pharm D, B Sc, M Sc, Biotechnology students

Fresh graduates seeking QC jobs

Working professionals wanting to upskill

QC/QA/Production/Microbiology team members

Anyone preparing for pharma job interviews

Why This Course Is Unique

Covers all pharma QC sections in detail Designed by industry experts with real-time experience Practical, job-oriented explanations Includes QA-friendly information without mixing medical devices Covers both formulation and API perspectives Helps you confidently face QC job interviews

After Completing This Course, You Will Be Able To:

Work confidently in any pharma QC laboratory

Perform key analytical and microbiological tests

Follow GLP, GDP, data integrity & regulatory expectations

Understand HPLC, GC, dissolution & impurity profiling

Handle OOS, deviations, CAPA & audit situations

Build a strong career path in Quality Control

Salary Summary – Pharmaceutical Quality Control (QC)

India (Fresher – 0 to 3 Years)Typical Salary Range: ₹3 Lakh to ₹7 Lakh per year

USA (Entry Level – 0 to 2 Years)Typical Salary Range: $45,000 to $65,000 per year(Approx. ₹38 Lakh to ₹55 Lakh per year equivalent)

United Kingdom (Entry Level – 0 to 2 Years)Typical Salary Range: £24,000 to £40,000 per year(Approx. ₹25 Lakh to ₹42 Lakh per year equivalent)

European Union (Entry Level – 0 to 2 Years)Typical Salary Range: €34,000 to €45,000 per year(Approx. ₹28 Lakh to ₹38 Lakh per year equivalent)

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Videos

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Why Temperature and Humidity Are Critical Environmental Parameters in Pharmaceutical Quality Control