Posted:1 day ago|
Platform:
On-site
Part Time
Responsible for document management like BMRs, BPRs, master SOPs etc..
Responsible for preparation & review of the master documents of production.
Responsible to ensure UAF working in area.
Responsible for the handling of change control, deviations, investigation & CAPA, etc.
Responsible to check that all the records and logbooks related to manufacturing, Sterilization, washing and sterilization of equipment’s.
Responsible for preparation, review, revision, control, and implementation of standard operating procedures of sterile manufacturing department.
Responsible to ensure cleaning and sanitization of General & Controlled area.
Inform immediately to department functional head for any observation/disturbance with respect to documents and machines found in area.
Responsible for monitoring all the activities related to General & Control area.
Responsible to give training to all the subordinates, technicians, and operators of the department.
Responsible to keep area updated with all the document and cleaning.
Responsible to provide guidance to subordinates.
Responsible to be fully familiar with machine and activities in his work.
Qualification - B.Sc. /M.Sc. / B. Pharm / M.Pharm
Amneal Pharmaceuticals
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