- Ensure compliance with cGMP practices and maintain accurate documentation.
- Handle USFDA audits and ensure the facility is audit-ready at all times.
- Independently enter data in Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
- Manage the assigned manufacturing area independently, ensuring smooth operations and adherence to quality standards.
- Operate and monitor machines such as HVAC systems, Capsule Filling machines, and Autocartonator.
- Adhere to shift schedules and be ready to work in shifts as per production requirements.
Desired Candidate Profile:
- Qualification: ITI / +2
- Experience: 2 to 6 years in Tablet Manufacturing within an OSD (Oral Solid Dosage) Plant.
- Willingness to work in shifts.
- Solid understanding of OSD manufacturing processes, cGMP compliance, and documentation practices.
📌 Machine Operators (Una)
🏢 Stanford Laboratories
📍 Una
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