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. • To perform the in-process checks as per BMR requirement and frequency. • To maintain the quality culture within the department.

📌 Technical Assistant (India)
🏢 Cadila Pharmaceuticals
📍 India