Senior Executive - Manufacturing
Amneal Pharmaceuticals
Date: 5 days ago
City: Ahmedabad, Gujarat
Contract type: Full time
Job Responsibility
JOB DESCRIPTION
3 Responsible to attend the training as per training schedule and to ensure the training as per TNI.
4 Responsible to work as per standard operating procedures, in general area of sterile manufacturing department.
5 Responsible for preparation, review, revision, control and implementation of Standard Operating Procedures of General Area in Sterile Manufacturing Department.
6 Responsible for BPR Preparation.
7 Responsible to ensure that all equipments and lines are in validated and calibrated status.
8 Responsible to check that all the records and log books related to general area and equipment of packaging, inspection area.
9 Responsible to give training to all the subordinates, technicians and operators of the department.
10 To follow the cGMP, Good Document Practice and discipline in the department.
11 Responsible for document handling of Packing, and Inspection.
12 Responsible for monitoring of all the activities related to packing, and inspection.
Qualifications
Education: B.Sc., B.Pharma, M.Sc., M.Pharma
Total Experience - 2 - 7 Year in sterile manufacturing plant
JOB DESCRIPTION
- 1 Responsible for preparation of packaging planning on monthly and also daily as per the requirement and availability of materials.
3 Responsible to attend the training as per training schedule and to ensure the training as per TNI.
4 Responsible to work as per standard operating procedures, in general area of sterile manufacturing department.
5 Responsible for preparation, review, revision, control and implementation of Standard Operating Procedures of General Area in Sterile Manufacturing Department.
6 Responsible for BPR Preparation.
7 Responsible to ensure that all equipments and lines are in validated and calibrated status.
8 Responsible to check that all the records and log books related to general area and equipment of packaging, inspection area.
9 Responsible to give training to all the subordinates, technicians and operators of the department.
10 To follow the cGMP, Good Document Practice and discipline in the department.
11 Responsible for document handling of Packing, and Inspection.
12 Responsible for monitoring of all the activities related to packing, and inspection.
Qualifications
Education: B.Sc., B.Pharma, M.Sc., M.Pharma
Total Experience - 2 - 7 Year in sterile manufacturing plant
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