In the pharmaceutical industry, these departments play crucial roles in ensuring the production, quality, safety, and efficiency of medicines. Here's an overview of each:

1. Operator

   • Handles machinery and equipment for manufacturing pharmaceutical products.
   • Ensures compliance with Good Manufacturing Practices (GMP).
   • Maintains safety and hygiene standards.

2. Production Chemist

   • Supervises the manufacturing process of drugs.
   • Ensures batch production follows Standard Operating Procedures (SOPs).
   • Monitors raw materials, process conditions, and final product quality.

3. Quality Control (QC)

   • Tests raw materials, intermediates, and finished products.
   • Ensures compliance with pharmacopeial standards (e.g., USP, BP, IP).
   • Conducts stability studies and microbiological testing.

4. Quality Assurance (QA)

   • Oversees documentation, SOPs, and regulatory compliance.
   • Conducts internal audits and ensures adherence to GMP.
   • Manages deviations, CAPA (Corrective and Preventive Actions), and validation processes.

5. Research & Development (R&D)

   • Develops new drug formulations and improves existing ones.
   • Conducts pre-formulation, formulation, and analytical studies.
   • Works on regulatory submissions and patents.

6. Store (Warehouse & Inventory Management)

   • Manages raw materials, packaging materials, and finished goods inventory.
   • Ensures proper storage conditions (temperature, humidity, etc.).
   • Maintains records of material usage and stock levels.

Each department is interconnected to ensure the safe, effective, and compliant production of pharmaceuticals. Let me know if you need further details on any specific role