Roles Overview

The selected candidates will be responsible for production activities related to API, Intermediates, and Bulk Drug manufacturing. The role involves operating production equipment, monitoring manufacturing processes, maintaining GMP compliance, and ensuring production targets are achieved safely and efficiently.

Job Responsibilities

• Execute production operations as per approved procedures.
• Operate and monitor manufacturing equipment.
• Maintain batch manufacturing records.
• Follow GMP, safety, and compliance requirements.
• Coordinate with QA, QC, and Engineering departments.
• Ensure timely completion of production schedules.
• Report deviations and abnormalities during manufacturing.
• Maintain cleanliness and housekeeping in production areas.

Key Deliverables

• Safe and efficient production operations.
• Compliance with GMP requirements.
• Timely completion of production batches.
• Accurate documentation practices.
• Achievement of production targets.
• Reduction of process deviations and errors.

Benefits Offered

• Free Transportation
• Subsidized Canteen
• Free Group Mediclaim
• Additional Employee-Friendly Benefits

How to Apply

Interested candidates meeting the qualification and experience requirements can directly attend the walk-in interview on the scheduled Date(13 June 2026) and Time (10:00 AM onwards). Carry the following documents:

• Updated Resume/CV
• Experience Certificate(s)
• Educational Certificates / Mark Sheets
• Aadhaar Card Copy
• PAN Card Copy
• Latest Passport Size Photos
• 3 moths Pay slips