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JSS Academy of Higher Education & Research Online
AICTE Approved
NAAC A++
UGC Approved
NAAC A++ deemed university, NIRF #38 Overall, since 2008.
16+ Yrs Legacy, NAAC A++ Rated, and NIRF #38 Overall
Last few seats left for July batch
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Fresh Graduates
Kick-start your management career at the most affordable fee in the industry

Career Switcher
Pivot from technical or non-management roles into business leadership

Entrepreneur
Build your business with structured knowledge in strategy, finance and operations

Working Professional
Upskill without quitting your job with flexible weekend classes
Class 10/12
Student or early professional with no formal vocational or technical training
12–24 Months
Practical skill-building, industry tools, vocational training & live projects

₹3.5 LPA
Technical Executive / Vocational Specialist — 120+ hiring partners
Class 10/12
Student or early professional with no formal vocational or technical training
12–24 Months
Practical skill-building, industry tools, vocational training & live projects

₹3.5 LPA
Technical Executive / Vocational Specialist — 120+ hiring partners
Student Category:
Indian
Eligibility:
Any graduates pursuing in the field of Pharmaceutical Sciences, Medical Sciences, Veterinary Sciences, Biotechnology, Microbiology and Life Sciences from any recognized institution.
Document Required:
Marksheets, Passport-size photograph, Aadhaar (Indian) / Passport (Foreign). Application fee required at submission.
| Academic Level | Min Score (General) | Min Score (Reserved) | Student Category | Eligibility | Document Required |
|---|---|---|---|---|---|
| Graduate (Pharma/Med/Vet/Biotech/Microbio/Life Sciences) | -- | -- | Indian | Any graduates pursuing in the field of Pharmaceutical Sciences, Medical Sciences, Veterinary Sciences, Biotechnology, Microbiology and Life Sciences from any recognized institution. | Marksheets, Passport-size photograph, Aadhaar (Indian) / Passport (Foreign). Application fee required at submission. |
Unit 1: cGMP — Evolution, Principles, US cGMP Part 210 & 211, Schedule-M, WHO-GMP, US FDA Pharma Manufacturing Guidelines, EC Directives 91/356/EEC
Unit 2: Quality (TQM, QbD, Six Sigma, OOS); Validation Types & Qualification; ICH/WHO Stability; ISO 13485; GLP; QA Unit; SOPs; Change Control; CAPA; NABL
Unit 3: Documentation in Pharma Industry — EPDB, PDP, PDR, BMR, BPR, MFR, Distribution Records, DMF, CoA, Site Master File, CMC, CTD/eCTD Format
Unit 4: Drugs and Cosmetics Act 1940 & Rules 1945 — DPCO, NPPA, Schedules, CDSCO, State Licensing, Regulatory Dossier Filing, Drug Import/Manufacture/Sale/Labelling/Packing, Cosmetic Registration
Unit 5: Lifecycle Management — PAS, SUPAC, CBE-30, Annual Report, Post-marketing Reporting, Post-approval Labeling, FDA Inspection, EIR, Warning Letters, Recalls, ISO Risk Mgmt
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