Description
Responsible for document management like BMR’s, BPR’s, master SOP’s 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 give training to all the subordinates, technicians and operators of the department.
Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HOD’s instruction and guidance.
Responsible for line clearance activity before commencing the operations.
Responsible to check that all the records and logbooks related to aseptic manufacturing, vial filling and vial sealing machine.
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 & Aseptic 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 & Aseptic area.
Responsible to ensure qualification and calibration status of equipment and instruments to avoid due/overdue.
Responsible to ensure scheduled activity of respective area/equipment/instruments.
Responsible to attend training as per schedule and to ensure training and work as per TNI.
Follow the cGMP, Positive Document Practice and discipline in the Company Premises.

Skills:
Filling, stoppering and sealing | Expert
Equipment Operation & Cleaning (CIP/SIP) | Proficient
Dispensing | Proficient
Sterilization through Autoclave | Proficient
Mixing | Proficient
Decartoning | Expert
Washing | Proficient
Terminal Sterilization | Proficient
Positive Manufacturing Practice (GMP) | Proficient
Batch Documentation and Record Review | Proficient
Cleaning & Line Cl

📌 Senior Executive Filling Inj Manufacturing Mehsana
🏢 Amneal
📍 Mehsana