Production Department (Officer)

Encube Ethicals; South Goa District; On-site; INR 502,000 - 725,000; Full time

Job summary

Encube Ethicals in Goa is seeking a Production Supervisor (B.Pharm / M.Pharm) to supervise activities as per assignment, ensure cGMP compliance, and maintain batch records and documentation.

The role requires good communication and coordination skills, willingness to work in shifts, and a focus on optimizing manpower and equipment utilization in the filling/packing area.

Qualifications

• B.Pharm or M.Pharm with basic knowledge of cGMP and production processes.
• Strong communication, documentation and coordination skills.
• Willingness to work in shifts as per operational requirements.
• Pharma knowledge and good theoretical understanding.

Responsibilities

• Supervise activities as per assignment by Executive/Assistant Manager.
• Maintain storage conditions and documentation as per statutory and customer requirements.
• Adherence to cGMP requirements in the assigned section.
• Check in process done in log books.
• Handling rejections on line.
• Daily Line clearance, Batch change over & product change over on decartoning / filling /packing area.
• Timely completion of batch records and other documents in assigned section.
• Organize for proper maintenance of the equipment in assigned section.
• Organize for proper disposal of rejected material or waste generated during the processing.
• Optimize the utilization of manpower and equipment in assigned section.
• Review and update the GMP documentation in assigned section.

Skills

cGMP knowledge

Production processes

Communication

Documentation

Coordination

Education

B.Pharm

M.Pharm

Job description

Responsibilities and Tasks:

• Supervising the activities as per the assignment by Executive/Assistant Manager
• Maintaining proper storage conditions and documentation as per the statutory and customer requirements.
• Adherence to cGMP requirements in the assigned section.
• Check in process done in log books.
• Handling rejections on line.
• Daily Line clearance, Batch change over & product change over on decartoning / filling /packing area.
• Timely completion of batch records and other documents in assigned section.
• Organize for proper maintenance of the equipment in assigned section.
• Organize for proper disposal of rejected material or waste generated during the processing.
• Optimize the utilization of manpower and equipment in assigned section.
• Review and update the GMP documentation in assigned section.

Preferred Candidate Profile:

• Qualification: B. Pharm / M. Pharm
• Basic knowledge of cGMP and production processes
• Good communication, documentation, and coordination skills
• Willingness to work in shifts as per operational requirements
• Should possess good communication skills, theoretical and pharma knowledge