Job Description

Job Purpose:
To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation.
Key Responsibilities:

• Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders.
• Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR).
• Monitor granulation parameters and adjust settings to maintain product quality.
• Perform in-process checks (e.g., moisture content, granule size) and document results accurately.
• Clean and maintain equipment and work areas as per SOPs.
• Execute machine changeovers and line clearance activities.
• Identify and report deviations or equipment malfunctions to the supervisor.
• Ensure compliance with cGMP, safety, and environmental regulations.
• Participate in continuous improvement and troubleshooting initiatives.

• ITI / Diploma / B.Sc or equivalent; technical diploma preferred.
• 4-6 years of experience in pharmaceutical manufacturing, preferably in granulation.
• Familiarity with cGMP, USFDA guidelines, and pharmaceutical documentation practices.
• Ability to read and interpret batch records and SOPs.
• Basic computer skills and understanding of production documentation.

• Attention to detail and strong documentation habits.
• Mechanical aptitude for operating and troubleshooting equipment.
• Team player with good communication skills.
• Forklift certification (if required for material handling).