Jobs at RPG Life Sciences

RPG Life Sciences is seeking an experienced Executive – Production to support pharmaceutical manufacturing operations at its Ankleshwar-F2 facility. The role involves preparing and implementing Standard Operating Procedures (SOPs), maintaining Batch Manufacturing Records (BMRs) and production documentation, monitoring calibration and validation activities, ensuring in-process quality checks, controlling batch reconciliation and manufacturing yields, and maintaining compliance with regulatory requirements and quality systems. The position also includes handling deviations, change controls, OOS investigations, CAPA through the EQMS system, coordinating employee training, and supervising inspection activities.

• Preparation, periodic review, revision, and implementation of Standard Operating Procedures (SOPs) of production department.
• Preparation of BMR as and when required.
• Maintain online documentation related to production activities like BMR's, log books, checklist, balance verification and daily records.
• Monitoring of calibration, verification and support validation activities in production department.
• To prepare and execute qualification protocol of production department.
• Monitor, control and check in process checks during processing related to inspection area.
• Ensuring proper segregation / identification and labelling of batches.
• Batch reconciliation and yield control at various stages of manufacturing.
• Monitoring of environmental conditions during process in manufacturing area.
• Compliance to all regulatory requirements and quality system in the manufacturing department.
• Initiation & investigation of deviation / change control / OOS (Phase-II) of production department.
• Handling of EQMS System for initiation of deviation / change control, CAPA of production department.
• Implementation of training needs identification as per training calendar in production department as a department training coordinator, and coordination with concerned department to ensure effective training.
• Supervision of Inspection activity.

• 2–6 years of relevant experience.
• Knowledge of Standard Operating Procedures (SOPs) and Batch Manufacturing Records (BMRs).
• Production documentation and logbook maintenance.