Cadila Pharma

• Ensure the c-GMP Compliance and schedule M compliance in production.
• Ensure the completion of production targets with zero quality issue.
• Ensure the compliance of inspection /Audit in coating area and follow of procedures/SOPs.
• To work at designated place in Coating & Capsule machine where they are trained to work for as
allocated by supervisor.
• To make and attach the status labeling on the equipment, utensils and miscellaneous items during
operation/cleaning and after operation/cleaning.
• To follow the SOPs, BMR procedures while performing the activity in accurate form what is
mentioned.
• To document the process with real time (i.e. start time, end time, process parameters recording,
process monitoring status, in-process checks etc.) in the Sequential log book, BMR and SOP annexure.
• To perform the effective cleaning of area & equipment as per the SOPs and to place the equipment
parts, change parts at designated location with proper status labeling.
• To participate in training program.
• To maintain the equipment’s health and provide intimation of any predictive breakdown or missing
parts or damaged parts to supervisor.
• To continue monitoring of the process since starting to end and timely crosschecking the quality of
product during running process as per MMD-I/SOP with documented evidence.
• To perform the in-process checks as per BMR requirement and frequency.
• To maintain the quality culture within the department.

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