Production Shift In-Charge

Drlogy; India; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Drlogy in India is looking for an experienced Production Shift In-Charge to oversee pharmaceutical manufacturing operations during assigned shifts. The ideal candidate will ensure compliance with GMP, safety, and production standards while coordinating manpower and monitoring production workflows.

Key responsibilities include supervising operations, maintaining batch records, and collaborating with QA/QC teams for quality support. This role offers an opportunity to contribute to process optimizations and efficiency improvements in a dynamic manufacturing environment.

Qualifications

• Extensive experience in supervising pharmaceutical manufacturing operations.
• Skilled in maintaining compliance with GMP and safety standards.
• Experience in monitoring production workflows and batch processes.

Responsibilities

• Supervise shift-wise pharmaceutical production operations efficiently.
• Ensure compliance with GMP and manufacturing SOPs consistently.
• Monitor batch processing and production workflow activities regularly.
• Coordinate manpower allocation and shift scheduling effectively.
• Maintain manufacturing records and operational documentation accurately.
• Monitor machine performance and operational efficiency consistently.
• Ensure timely availability of raw materials and production consumables.
• Coordinate with QA and QC teams for quality compliance support.
• Investigate process deviations and implement corrective actions promptly.
• Maintain cleanliness and safety within manufacturing areas.
• Support troubleshooting and breakdown handling activities efficiently.
• Participate in audits and regulatory inspections.
• Monitor production KPIs and shift performance metrics regularly.
• Train operators and staff on GMP and operational procedures.
• Contribute to process optimization and productivity improvement initiatives.

Skills

Supervision of Pharmaceutical Operations

GMP Compliance

Batch Monitoring

Operational Planning

Manpower Coordination

Quality Management

Job description

Experienced Production Shift In-Charge

Experienced Production Shift In-Charge responsible for supervising pharmaceutical manufacturing operations during assigned shifts while ensuring compliance with GMP, safety, and production standards. Skilled in manpower coordination, batch monitoring, process supervision, and operational planning. Adept at maintaining production efficiency, product quality, and smooth workflow management within pharmaceutical manufacturing environments.

• Supervise shift-wise pharmaceutical production operations efficiently.
• Ensure compliance with GMP and manufacturing SOPs consistently.
• Monitor batch processing and production workflow activities regularly.
• Coordinate manpower allocation and shift scheduling effectively.
• Maintain batch manufacturing records and operational documentation accurately.
• Monitor machine performance and operational efficiency consistently.
• Ensure timely availability of raw materials and production consumables.
• Coordinate with QA and QC teams for quality compliance support.
• Investigate process deviations and implement corrective actions promptly.
• Maintain cleanliness and safety within manufacturing areas.
• Support troubleshooting and breakdown handling activities efficiently.
• Participate in audits and regulatory inspection activities.
• Monitor production KPIs and shift performance metrics regularly.
• Train operators and staff on GMP and operational procedures.
• Contribute to process optimization and productivity improvement initiatives.