
The Jharkhand Public Service Commission (JPSC) has officially opened the gateway for high-calibre medical and pharmacy professionals to secure a prestigious Group ‘B’ Gazetted position through the JPSC Drug Inspector Recruitment 2026 (Advt. No. 12/2025). This highly competitive examination is designed to identify experts capable of upholding the stringent standards of the Drug & Cosmetics Act, demanding a deep mastery of pharmaceutical sciences and regulatory frameworks.
With a rigorous selection process comprising five comprehensive objective papers and a high-stakes personality test, candidates must navigate a vast 1100-mark evaluation system that covers everything from advanced Microbiology to Pharmaceutical Jurisprudence. For those aspiring to influence the healthcare landscape of Jharkhand, mastering this detailed syllabus is not just a requirement—it is the essential blueprint for a successful career in public service.
The following table provides a high-level summary of the subjects covered in the written examination.
| JPSC Drug Inspector Syllabus Overview | ||
| Paper | Subject Area | Key Focus Topics |
| Paper I | Pharmaceutics / General Medicine | Dosage forms, manufacturing, and clinical pharmacy. |
| Paper II | Microbiology | Sterilisation, immunology, and microbial assays. |
| Paper III | Pharmacology | Pharmacokinetics, systemic pharmacology, and toxicology. |
| Paper IV | Pharmaceutical Chemistry / Biochemistry | Drug synthesis, biochemical pathways, and analysis. |
| Paper V | Pharmaceutical Jurisprudence & Ethics | Drugs & Cosmetics Act, regulatory duties, and legal standards. |
This paper covers the science of dosage form design and the medical application of drugs.
Pharmaceutical Formulations: Study of tablets, capsules, liquids, and parenterals.
Manufacturing Processes: Unit operations and large-scale production techniques.
Clinical Pharmacy: Drug interactions, hospital pharmacy management, and dispensing.
General Medicine: Basics of human diseases and the therapeutic management of common ailments.
This section focuses on the biological safety and testing of pharmaceutical products.
Sterilisation Techniques: Methods used to ensure products are free from viable microorganisms.
Immunology: Production and testing of vaccines and sera.
Microbiological Assays: Techniques for testing the potency of antibiotics and vitamins.
Microbial Control: Monitoring contamination in pharmaceutical environments.
Pharmacology examines the effects of drugs on the human body and vice versa.
Pharmacokinetics: Absorption, distribution, metabolism, and excretion (ADME) of drugs.
Systemic Pharmacology: Detailed study of drugs acting on the CNS, CVS, and gastrointestinal tract.
Chemotherapy: Clinical use of anti-infective and anticancer agents.
Toxicology: Identification and treatment of poisoning and adverse drug reactions.
This paper combines chemical analysis with the study of life's molecular processes.
Medicinal Chemistry: Structure-activity relationships and the synthesis of therapeutic agents.
Biochemistry: Metabolism of carbohydrates, lipids, and proteins.
Enzymology: Study of enzymes, vitamins, and hormones in health and disease.
Analytical Techniques: Methods for identifying and quantifying drug substances.
This section is vital for regulatory roles, focusing on the laws governing the pharmacy profession.
Drugs and Cosmetics Act (1940): Comprehensive knowledge of the Act and the 1945 Rules.
Pharmacy Act (1948): Regulations governing pharmacy education and registration.
Inspectorate Duties: Legal powers, search and seizure procedures, and reporting duties.
Related Statutes: Narcotic Drugs and Psychotropic Substances (NDPS) Act and Drug Price Control Orders (DPCO)