Master Core Pharma. Launch Your Industry Career
Scholavar bridges the gap between what you learn in college and what pharma companies actually need. Get industry-ready skills in GMP, Quality Control, Quality assurance, Regulatory Affairs, Formulation Development, and Analytical Research taught by professionals who work in the field every day. Land your first pharma job with confidence, or accelerate your career in manufacturing, R&D, QC, QA, or Regulatory roles across India’s booming pharmaceutical sector.
Why Pharma Companies Choose Scholavar-Trained Talent
Every year, thousands of Bachelor and Masters of pharmacy and Science graduates enter the job market—but most lack the hands-on, compliance-ready skills that pharma companies demand. Companies spend months training fresh hires on GMP protocols, batch record documentation, deviation handling, and regulatory submissions.
That's where Scholavar changes everything.
Our learners graduate job-ready because they've already mastered:
✓ Good Manufacturing Practices (GMP) for pharma operations
✓ Quality Control testing and Quality Assurance protocols
✓ Regulatory Affairs—from dossier preparation to CDSCO submissions
✓API Manufacturing and Synthetic Chemistry workflows
✓ Formulation Development from lab to production scale
✓ Analytical Method Development, Validation, and Transfer
You don't just learn theory—you work through real-world case studies, SOPs, and compliance scenarios used in actual pharma plants across India
5 Core Pharma Tracks That Get You Hired
Choose your path based on where you want to work in the pharmaceutical industry
Quality Assurance & Quality Control
Master GMP compliance, batch record review, deviation management, CAPA, internal audits, and quality systems. Perfect for QA Officers, QC Analysts, and Quality Managers.
Regulatory Affairs
Learn dossier preparation, regulatory submissions (CDSCO, USFDA, EMA), product registrations, license management, and audit readiness. High-demand, high-salary career path.
Manufacturing & GMP Operations
Understand pharma production workflows, equipment qualification, process validation, material handling, manufacturing documentation, and plant operations under GMP.
Formulation & Analytical Development
Gain expertise in dosageform design, formulation optimization, scale-up, analytical method development, validation, stability studies,laboratory investigations and technology transfer.
API Synthesis & Synthetic Chemistry
Deep dive into API manufacturing, synthetic routes, reaction optimization, process chemistry, impurity profiling, and scaling chemical processes for commercial production.
Learn from Professionals Who Work in Pharma Every Day
Our instructors aren't just teachers—they're working professionals from leading pharmaceutical companies across India. They bring real-world experience from
production floors, QC labs, regulatory desks, and R&D centers. They know exactly what companies look for because they're the ones doing the hiring, training, and auditing.
What makes our experts different:
●Currently working in pharma manufacturing, quality, R&D, or regulatory roles
●Hands-on experience with USFDA inspections, WHO-GMP audits, and Schedule M compliance
●Practical knowledge of Indian pharma operations, not just textbook theory
●Understanding of what fresh graduates struggle with—because they mentor them daily
When you learn from Scholavar, you're learning from the people who actually run pharma operations in India.
The Scholavar Difference
How We Prepare You for Real Pharma Roles
Industry-Aligned Curriculum
Every module is built around actual pharma workflows—from receiving raw materials to final batch release. Learn the skills that QA managers, production supervisors, and regulatory specialists use daily in companies like Sun Pharma, Dr. Reddy's, and Cipla.
Visual-First Learning
Say goodbye to boring PDFs. Our courses use rich visuals, flowcharts, real batch records, animated GMP workflows, and video demonstrations. Complex processes like validation protocols and deviation investigations become crystal clear.
Compliance-Ready from Day One
Master documentation discipline, understand WHO-GMP and Schedule M requirements, and learn how to handle OOS investigations, CAPA, and change controls—the non-negotiables for any pharma job in India.
Career Acceleration
Whether you're a final-year B.Pharm student aiming for your first QC role, or a production chemist targeting a Quality assurance domain, Scholavar gives you the demonstrable skills that get you hired and promoted faster.