Technical Production Assistant

Cadila Pharmaceuticals; Udaipur District; On-site; INR 180,000 - 240,000; Full time

Job summary

Cadila Pharmaceuticals is seeking personnel to uphold hygienic conditions before entering manufacturing areas and to follow entry-exit procedures. You will participate in training as required and perform on-line in-process checks according to SOP.

You will clean and operate vessels, autoclaves, and filtration equipment, maintain records, monitor conditions, and ensure cgmp-compliant documentation and logs in the relevant production areas.

Responsibilities

• Maintain proper hygienic conditions before entering manufacturing area.
• Follow manufacturing area entry-exit procedure and participate in training as needed.
• Perform on-line in-process checks per SOP.
• Perform area cleaning per SOP and maintain records.
• Clean and operate manufacturing/holding vessels as per SOP and maintain records.
• Clean, operate and load prepare autoclave as per routine and production plan.
• Perform filter integrity tests of hydrophilic/hydrophobic and disk filters as per routine.
• Conduct particle monitoring per routine and production plan; clean and operate vial capping machine and maintain records.
• Ensure proper status labeling of area and equipment per SOP.
• Check calibration schedule of measuring instruments and inform supervisor.
• Record TEMP/RH in aseptic and processing areas; participate in equipment qualification activities.
• Inform supervisor of any deviation from approved process.
• Follow Good Documentation Practice during documentation.
• Maintain area and equipment logs as per SOP; comply with cgmp.
• Handle additional responsibilities assigned by HOD.

Job description

Role & responsibilities :

• To maintain proper hygienic condition before entering to manufacturing area.
• To follow manufacturing area entry exit procedure properly. To take part in training whenever necessary.
• To perform on line in-process checks as per SOP.
• To perform area cleaning as per SOP and maintain records.
• To perform cleaning and operation of Mfg./Holding vessels as per SOP and maintain record.
• To perform cleaning, operation and load preparation of autoclave as per routine and production plan.
• To perform filter integrity of hydrophilic/hydrophobic and disk filters as per routine and production plan.
• To perform particle monitoring as per routine and production plan. To perform cleaning and operation of vial capping machine and maintain the record.
• To perform proper status labeling of area and equipment as per SOP.
• To check calibration schedule of all measuring instruments and inform to supervisor.
• To record TEMP/RH in the mfg. aseptic and processing areas. To take part in equipment qualification activities.
• To inform supervisor if any deviation from approved process.
• To follow Good documentation practice during documentation.
• To maintain area and equipment logs as per SOP. To follow plant wise cGMP compliance.
• To handle additional responsibility assigned by HOD.