Website Sun Pharma Ltd
Post Name: Officer – Granulation
Location: Dadra 1 – Operations Block A
Company: Sun Pharmaceutical Industries Ltd
Job Purpose:
To supervise and coordinate all granulation activities, ensuring compliance with cGMP, safety, and quality standards while meeting production targets and supporting continuous improvement initiatives.
Key Responsibilities:
Supervise daily granulation operations including fluid bed drying, high shear mixing, wet granulation, and blending.
Execute production activities as per the approved production plan and batch manufacturing records (BMR).
Ensure adherence to cGMP, safety, hygiene, and environmental standards.
Monitor equipment performance and coordinate with maintenance for preventive and corrective actions.
Review and maintain production documentation including BMRs, logbooks, and deviation reports.
Train and guide operators on SOPs, equipment handling, and safety protocols.
Coordinate with QA, QC, R&D, and engineering teams for validations, investigations, and new product introductions.
Participate in audits, CAPA implementation, and continuous improvement projects.
Ensure optimal utilization of manpower and resources.
Qualifications:
Education: Bachelor’s degree in Pharmacy.
Experience: Minimum 5 years in pharmaceutical manufacturing with at least 2–3 years in a supervisory role, preferably in granulation.
Skills:Strong technical knowledge of granulation processes and equipment.
Good understanding of cGMP, USFDA regulations, and documentation practices.
Excellent leadership, communication, and problem-solving skills.
Proficiency in handling deviations, investigations, and compliance documentation
