Assistant Manager-Manufacturing
Amneal Pharmaceuticals
Date: 2 weeks ago
City: Ahmedabad, Gujarat
Contract type: Full time
Job Description
Responsible for line clearance activity before commencing the operations
Responsible to follow the preventive maintenance schedule of machine
Responsible for cleaning and sanitization of visual inspection and Packing area.
Responsible to operate the machines .
Responsible to fill the log of general area as per SOP and work execution. Responsible to follow cGMP, GDP, and discipline in the department and to ensure that all employees follow the same.
Responsible to ensure that all equipment’s and lines are in validated and calibrated status.
Responsible to prepare daily production report as per the production achieved.
Responsible for preparation of production planning on monthly and daily as per the requirement and availability of materials.
Responsible for the handling of change control, deviations, CAPA, investigation etc.
Responsible for document management like BMRs, BPRs, master SOPs etc..
Responsible for preparation and review of protocols and reports based on the requirements.
Responsible for preparation and review of protocols and reports based on the requirements.
Responsible for preparation, review, revision, control, and implementation of standard operating procedures of sterile manufacturing department.
Responsible for line clearance activity before commencing the operations like manufacturing, Sterilization, filling etc..
Responsible to check that all the records and logbooks related to manufacturing, filling, garment washing and drying & sterilization of equipment’s .
Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance.
Responsible to give training to all the subordinates, technicians, and operators of the department. Responsible to update on self-hygiene.
Responsible to attend the training as per training schedule and to ensure training as per TNI.
Qualifications
Qualification - M.Sc. / B. Pharm / M.Pharm
Responsible for line clearance activity before commencing the operations
Responsible to follow the preventive maintenance schedule of machine
Responsible for cleaning and sanitization of visual inspection and Packing area.
Responsible to operate the machines .
Responsible to fill the log of general area as per SOP and work execution. Responsible to follow cGMP, GDP, and discipline in the department and to ensure that all employees follow the same.
Responsible to ensure that all equipment’s and lines are in validated and calibrated status.
Responsible to prepare daily production report as per the production achieved.
Responsible for preparation of production planning on monthly and daily as per the requirement and availability of materials.
Responsible for the handling of change control, deviations, CAPA, investigation etc.
Responsible for document management like BMRs, BPRs, master SOPs etc..
Responsible for preparation and review of protocols and reports based on the requirements.
Responsible for preparation and review of protocols and reports based on the requirements.
Responsible for preparation, review, revision, control, and implementation of standard operating procedures of sterile manufacturing department.
Responsible for line clearance activity before commencing the operations like manufacturing, Sterilization, filling etc..
Responsible to check that all the records and logbooks related to manufacturing, filling, garment washing and drying & sterilization of equipment’s .
Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance.
Responsible to give training to all the subordinates, technicians, and operators of the department. Responsible to update on self-hygiene.
Responsible to attend the training as per training schedule and to ensure training as per TNI.
Qualifications
Qualification - M.Sc. / B. Pharm / M.Pharm
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