Production Officer

Drlogy; Dehradun; On-site; INR 300,000 - 500,000; Full time

Job summary

Drlogy in Dehradun, India is seeking a Skilled Production Officer to oversee manufacturing activities and ensure compliance with GMP and pharmaceutical standards. You will manage batch processing, documentation, and production coordination.

The ideal candidate is experienced in maintaining production efficiency and quality compliance, facilitating smooth operations, and reporting production targets regularly.

Qualifications

• Experience in managing manufacturing activities and production processes.
• Strong understanding of GMP and pharmaceutical standards.
• Adept at monitoring machine performance and ensuring timely availability of materials.

Responsibilities

• Monitor pharmaceutical production operations efficiently.
• Ensure compliance with GMP and manufacturing SOPs consistently.
• Maintain batch production records and operational documentation accurately.
• Coordinate manpower and production workflow activities.
• Support preventive maintenance and troubleshooting activities.

Skills

Batch processing

Documentation management

Process monitoring

Production coordination

GMP compliance

Job description

Skilled Production Officer responsible for managing manufacturing activities, monitoring production processes, and ensuring compliance with GMP and pharmaceutical standards. Experienced in batch processing, documentation management, process monitoring, and production coordination. Adept at maintaining production efficiency and ensuring smooth manufacturing operations.

• Monitor pharmaceutical production operations efficiently.
• Ensure compliance with GMP and manufacturing SOPs consistently.
• Maintain batch production records and operational documentation accurately.
• Coordinate manpower and production workflow activities.
• Monitor machine performance and report operational issues promptly.
• Ensure timely availability of raw materials and consumables.
• Coordinate with QA and QC teams for quality compliance support.
• Investigate production deviations and support corrective actions.
• Maintain cleanliness and safety within manufacturing areas.
• Follow pharmaceutical safety and operational procedures consistently.
• Support preventive maintenance and troubleshooting activities.
• Participate in audits and compliance inspection activities.
• Monitor production targets and workflow performance regularly.
• Train operators on production procedures and GMP practices.
• Contribute to process improvement and productivity enhancement initiatives.