Title: Technician - Granulation Block A

• 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.

  Qualifications:

  • 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.

  Preferred Skills:

  • 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).