Executive

Executive (E2)

Production (API)

7 to 10 Years

B. Pharma

Roles & Responsibilities

• Preparation & review of batch production records and equipment cleaning records.
• To ensure cleanliness of process equipment and plant.
• Initiating of Deviations, Change Controls, CAPA, Reprocessing through QAMS. Manufacturing investigation of Deviation, OOS, OOT and Batch failure. Keep the track of Deviations, CAPA, Change Controls, OOS, OOT, Batch failure from the plant and their timely closure.
• To ensure that all production activity is carried out as per Safety & GMP norms, Review of executed documents/batch production records.
• Conduct all tasks/ activities as per the applicable SOPs. Report any difficulty or deviation, Contributing towards the implementation of Harmonized cGMP practices
• Comply with all cGMP, GDP or any other regulatory requirement including EHS Requirement.
• Complete training on relevant SOPs and develop an understanding of the activities.
• Performing of calibration and monitoring of environmental conditions., Providing required trainings to plant employees.