Officer

Sun Pharma; Kalol; On-site; INR 420,000 - 600,000; Full time

Job summary

Sun Pharma in Kalol, Gujarat seeks a production Officer for the Tablet department (FBE) with a B. Pharma degree and at least 2 years' experience. The role focuses on daily production activities, GMP compliance, and collaboration with QA/QC to ensure product quality.

The Officer will be responsible for establishing procedures, coordinating with related departments, and training staff to optimize resources and maintain GMP standards across the manufacturing area.

Qualifications

• B. Pharma degree is required.
• 2+ years of experience in pharmaceutical production.

Responsibilities

• Overall production activities of the Tablet department (FBE) on day-to-day basis to meet production targets and GMP compliance.
• Assist other Officers in manufacturing and controlling functions of the Tablet department.
• Maintain/establish procedures in line with GMP guidelines and update existing procedures.
• Coordinate with QA/QC for product quality and validation activities.
• Train staff and operators in GMP practices and ensure resource optimization.
• Prepare daily reports on departmental activities.
• Handle calibration, qualification and validation of equipment or products.
• Procure machineries, spares, and materials for the department.
• Prepare destruction notes and maintain GMP records.
• Coordinate with Warehouse, MIS, and Engineering for materials and maintenance schedules.
• Prepare BMR/SOP/Protocol for new products/machines and revise as needed.

Skills

GMP compliance

Production management

Documentation

Staff training

Education

B. Pharma

Job description

Qualification : B. Pharma

Experience - 2+ years of experience

He is authorize to sign (as an Officer) :

1. cGMP documents as per following but not restricted to Equipment sequential log, Temperature and %RH record, Daily, weekly and Monthly cleaning records of Manufacturing area, Balance calibration, In process and under test approval label, Tool set cleaning record, Tool set utilization record etc.

Batch manufacturing Records. In process and Finished Product Test Requisitions.

Bulk quarantine / Staging room In-out record.

2. The Officer is responsible for overall production activities of the Tablet department (FBE section) on day to day basis in achieving total production requirements in quantity, quality and GMP compliance in department and Execution of production activity. To assist other Officer in manufacturing and controlling the functions related to Tablet department.

3. To assist establishing a system in accordance with Good Manufacturing Practice guidelines and Responsible for follow established / new procedures, maintaining and updating existing procedures in the department.

4. Responsible to co-maintain, coordinate for validation and GMP in all departments along with the Quality Assurance officer and to coordinate with Quality control department in matters relating to product quality.

5. Responsible for Good Manufacturing Practice/training to staffs and operator in the all department.

6. Responsible for optimization of the resources namely men, material and machine in respective department.

7. Make daily reports on day to day activities concerning the department.

8. Responsible for Calibration, qualification and validation activity of respective equipments or products.

9. Indenting and procurement of machineries, change parts, spares and material required in respective department.

10. Destruction note preparation and execution.

11. Maintaining the GMP documents like equipment logbooks, records of physical monitoring and housekeeping records.

12. Training the subordinates and manpower to meet the organizational goals and achieve GMP compliance.

13. Help the subordinates into standardize production activities to achieve better efficiency and product quality.

14. The Officer will handle the responsibility of Officer in his absence.

15. Coordinate with related departments like with Warehouse & MIS for the materials to achieve schedule plan, with the Engineering department for preventive maintenance schedule.

16. BMR/ SOP/ Protocol preparation for the new product/New machines. Revision of BMR / SOP /

Protocol whenever required and execution of BMR/ SOP/ Protocol.