Production Supervisor

Cadila Pharmaceuticals Limited; Udaipur; On-site; INR 201,000 - 335,000; Full time

Job summary

Cadila Pharmaceuticals Limited in Udaipur is seeking personnel to maintain hygienic conditions in manufacturing areas, follow entry-exit SOPs, and perform cleaning, disinfection, and equipment operations with strict record-keeping.

The role requires active participation in training, on-line checks, particle monitoring, autoclave and vial-line operations per production plans, and rigorous documentation to ensure GMP compliance.

Responsibilities

• Maintain proper hygienic condition entering manufacturing area.
• Follow manufacturing area entry-exit procedures.
• Participate in training when required.
• Prepare and filter disinfectant solution as per SOP.
• Record routine steps in tunnel SOP and related records.
• Clean using the three-bucket system; operate vial washing machine and maintain records.
• Operate vial filling machine and Lyophilized loading/unloading system; maintain records.
• Perform on-line in-process checks as per SOP.
• Clean the area as per SOP and maintain records.
• Operate glove port integrity tester and document.
• Monitor particle counts in Grade A and B areas.
• Operate autoclave per production plan and prepare loads.
• Check filter integrity of hydrophobic/hydrophilic and disk filters per production plan.
• Prepare and operate vial Capping machine and maintain records.
• Maintain proper status labels for area and equipment per SOP.

Job description

• To maintain proper hygienic condition be ("Ore entering to manufacturing area
• To follow manufacturing area entry exit procedure properly.
• To take part in training whenever necessary.
• To ensure and perform the Preparation and filtration of disinfectant solution as per
• SOP tunnel and automatic and record the per routine and the record.
• To ensure and perform the cleaning activity through three bucket system as per SOP ensure and perform cleaning and operation of vial washing machine/ Dehydrogenation maintain in the record.
• To perform and ensure the cleaning and operation of vial filling machine, Lyophilized loading/un loading system and maintain the record.
• To perform and ensure on line in-process checks as per SOP
• To perform and ensure area cleaning as per SOP and maintain records.
• To perform and ensure the cleaning and operation of glove port integrity tester documents.
• To perform and ensure the particle count monitoring in Grade-A and Grade-B area.
• To perform and ensure operation and load preparation of autoclave as production plan,
• To perform and ensure filter integrity of hydrophobic/ hydrophilic and disk tilters as production plan.
• PO perform and ensure cleaning and operation of vial capping machine and maintain
• To maintain proper status label of area and equipment as per SOP.