Senior Officer - Production (Projects) - Sterile/Injectable

Cipla; South Goa District; Vor Ort; INR 300.000 - 450.000; Vollzeit

Zusammenfassung

Cipla India in Goa is seeking a shift-based production operator to monitor and execute manufacturing activities, ensuring cGMP and safety norms while achieving daily production targets.

You will maintain BMRs and supporting documents, update CipDox and other systems, and operate SAP and QMS to ensure proper documentation and quality. Strong coordination with HSE will support a safe working environment.

Qualifikationen

• Follows cGMP and safety norms in production areas.
• Maintains standard process parameters per BMRs and documents.
• Operates SAP, CipDox and QMS systems.

Aufgaben

• Execute assigned tasks as per planned production activity to meet production targets for a shift.
• Regulate usage of consumables to minimize costs.
• Increase area efficiency by reducing downtime and optimizing equipment usage.
• Maintain documentation in BMRs and supporting documents for quality and compliance.
• Follow GMP and safety norms; review processes and documents for compliance.
• Operate SAP, CipDox and QMS; update systems with outputs.

Tools

SAP

CipDox

QMS

Jobbeschreibung

Job Purpose

Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets.

Key Accountabilities

• Execute assigned tasks as per planned production activity to meet production targets for a shift
• Regulate usage of consumables in the production process at optimum levels to save costs
• Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area
• Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality
• Ensure all operations are performed as per GMP & Safety norms by reviewing all processes and documents for compliance
• Ensure equipment, facility and block premises are maintained as per regulatory compliance
• Maintain system integrity by updating documentations and deviations on CipDox while performing operations
• Perform validation, qualification and calibration as per schedule and update output of all activities in the systems
• Prepare new documents and update existing documents as per GMP requirement
• Prepare manufacturing records and update online documentation to meet production and cGMP requirements
• Maintain online documentation and timely entries in BMR and supporting documents
• Prepare new documents and update existing documents as per GMP requirement
• Operate software such as SAP, CipDox and QMS
• Follow safe work processes and ensure safety appliances are utilised during production activities in shifts to create a safe working environment
• Ensure safety systems and procedures followed by the operators in the shift
• Ensure availability and usage of PPEs in the shift by coordinating with HSE department for requirements and shift schedule.
• Execute production activities in a shift by managing available resources to achieve production target
• Execute assigned tasks as per planned production activity to meet production targets for a shift
• Regulate usage of consumables in the production process at optimum levels to save costs
• Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area

Major Challenges

• Meeting shift targets due to unavailability of adequate resources. Overcome by efficient work load distribution and resource optimisation
• Meeting production targets due to lapses in knowledge transfer between shifts. Overcome by bridging gaps between inter-shift communication
• Maintaining cGMP requirements during system downtime. Overcome by coordinating with the engineering team and technical support team