Assistant / Associate - Batch Manufacturing

1 - 5 years

0 Lacs

Posted:1 day ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

As a Manufacturing Area Operator, your role involves attending training sessions as per schedule and ensuring that work is aligned with the Training Needs Identification (TNI). You will be responsible for monitoring and performing all activities within the Manufacturing area, including filling logs, Batch Manufacturing Records (BMRs), and other documents in accordance with Standard Operating Procedures (SOPs). Additionally, you will need to adhere to the preventive maintenance schedule for machines, instruments, and equipment in the manufacturing area, as well as oversee cleaning and sanitization processes. Key Responsibilities: - Attend training sessions as per schedule and align work with Training Needs Identification (TNI). - Monitor and perform all activities within the Manufacturing area. - Fill logs, Batch Manufacturing Records (BMRs), and documents in the area following SOPs. - Follow the preventive maintenance schedule for machines, instruments, and equipment. - Ensure cleaning and sanitization of machines, instruments, equipment, and the manufacturing area. - Conduct line clearance activities before operations, Clean-In-Place (CIP), and Steam-In-Place (SIP) of Vessel. - Operate machines such as Manufacturing Vessel and CIP module. - Report any observations or disturbances in the aseptic area to the supervisor immediately. - Maintain self-hygiene, cleaning, and sanitization standards in the area. - Update and maintain documentation as per SOPs. - Ensure the Unidirectional Airflow (UAF) is functioning properly. - Adhere to current Good Manufacturing Practice (cGMP), Good Documentation Practice, and discipline within the department. Qualifications Required: - High school diploma or equivalent. - Previous experience in a manufacturing or pharmaceutical environment preferred. - Strong attention to detail and adherence to SOPs. - Ability to work effectively in a team environment. - Knowledge of cGMP and other relevant regulations is a plus.,

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