Technical Assistant

Cadila Pharmaceuticals Limited

Dholka

On-site

INR 180,000 - 300,000

Full time

5 days ago

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Job summary

Cadila Pharmaceuticals Limited in India seeks a production operator in the Coating & Capsule area. You will ensure c-GMP and M compliance, strive for zero quality issues, and support inspections and SOP adherence.

You’ll work at the coating lines under supervision and carry out labeling, documentation, and cleaning tasks with meticulous record-keeping. The role requires following BMR and SOPs, participating in training, and maintaining equipment health while reporting issues to the supervisor.

Responsibilities

Ensure c-GMP compliance and schedule M compliance in production.
Ensure completion of production targets with zero quality issue.
Ensure compliance of inspection/audit in coating area and follow SOPs.
Work at designated place in Coating & Capsule machine as allocated by supervisor.
Attach status labeling on equipment, utensils and items during operation/cleaning and after.
Follow SOPs, BMR procedures and document activities accurately.
Document the process with real time data in log books, BMR and SOP annexure.
Perform effective cleaning of area & equipment as per SOPs and manage parts with labeling.
Participate in training programs.
Maintain equipment health and notify supervisor of issues.
Monitor process from start to end and conduct in-process quality checks with documented evidence.
Perform in-process checks as per BMR requirements and frequency.
Maintain a quality culture within the department.

Job description

Job Description:

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.