Senior Officer - Production
Sun Pharmaceutical Industries, Inc., Indiana, PA, United States
Company: Sun Pharmaceutical Industries Ltd
Title: Sr. Officer
Business Unit: SGO
Job Grade: G12B
Location: Halol-II
Key Responsibilities
Authorization to sign cGMP documents:
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.
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 Officers in manufacturing and controlling related functions.
Assist in establishing a system in accordance with Good Manufacturing Practice guidelines and responsible for following established
ew procedures, maintaining, and updating existing procedures in the department.
Co‑maintain and coordinate validation and GMP across departments along with the Quality Assurance officer, coordinating with the Quality Control department as required.
Responsible for Good Manufacturing Practice training of staff and operators in all departments.
Optimize resources namely men, material and machine in the respective department.
Make daily reports on-day‑to‑day activities concerning the department.
Responsible for calibration, qualification and validation activity of respective equipment or products.
Indenting and procurement of machineries, change parts, spares and material required in respective department.
Destruction note preparation and execution.
Maintain GMP documents like equipment logbooks, records of physical monitoring and housekeeping records.
Train subordinates and manpower to meet organizational goals and achieve GMP compliance.
Help subordinates standardize production activities to achieve better efficiency and product quality.
Handle officer responsibilities in his absence.
Coordinate with related departments such as Warehouse & MIS for materials to achieve schedule plan, and with Engineering department for preventive maintenance schedule.
Prepare BMR/SOP/Protocol for new product
ew machines, revise BMR/SOP/Protocol whenever required and execute.
Job Requirements
Educational Qualification: B.Pharma
Experience: 2+ years
Disclaimer:
The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
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Title: Sr. Officer
Business Unit: SGO
Job Grade: G12B
Location: Halol-II
Key Responsibilities
Authorization to sign cGMP documents:
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.
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 Officers in manufacturing and controlling related functions.
Assist in establishing a system in accordance with Good Manufacturing Practice guidelines and responsible for following established
ew procedures, maintaining, and updating existing procedures in the department.
Co‑maintain and coordinate validation and GMP across departments along with the Quality Assurance officer, coordinating with the Quality Control department as required.
Responsible for Good Manufacturing Practice training of staff and operators in all departments.
Optimize resources namely men, material and machine in the respective department.
Make daily reports on-day‑to‑day activities concerning the department.
Responsible for calibration, qualification and validation activity of respective equipment or products.
Indenting and procurement of machineries, change parts, spares and material required in respective department.
Destruction note preparation and execution.
Maintain GMP documents like equipment logbooks, records of physical monitoring and housekeeping records.
Train subordinates and manpower to meet organizational goals and achieve GMP compliance.
Help subordinates standardize production activities to achieve better efficiency and product quality.
Handle officer responsibilities in his absence.
Coordinate with related departments such as Warehouse & MIS for materials to achieve schedule plan, and with Engineering department for preventive maintenance schedule.
Prepare BMR/SOP/Protocol for new product
ew machines, revise BMR/SOP/Protocol whenever required and execute.
Job Requirements
Educational Qualification: B.Pharma
Experience: 2+ years
Disclaimer:
The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s).
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