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Associate - Manufacturing & Packing

0 years

0 Lacs

Posted:2 days ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Attend and ensure the training as per training schedule and TNIWork according to standard operating procedures in sterile manufacturing departmentPrepare, review, revise and control the Standard Operating Procedures of General Area in Sterile Manufacturing DepartmentPrepare BPRValidate and calibrate all equipment and linesRecord and check all the logbooks related to general area and equipment of packaging and inspection areaTrain all the subordinates, technicians and operators of the departmentComply with cGMP, Good Document Practice and departmental disciplineHandle document of Packing and InspectionMonitor all the activities related to packing and inspectionResponsible for line clearance activity before commencing the operationsResponsible to follow the preventive maintenance schedule of machineResponsible 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 .

Qualifications

ITI / B.Sc / Diploma

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Amneal Pharmaceuticals
Amneal Pharmaceuticals

Pharmaceutical Manufacturing

Bridgewater New Jersey

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