Roles & Responsibilities:
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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