Manager - Manufacturing

15 - 19 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 candidate for the position, you will be responsible for various key activities in the sterile manufacturing department. Your job responsibilities will include: - Updating on self-hygiene. - Preparation, review, revision, control, and implementation of standard operating procedures. - Preparation and review of master production documents. - Preparation and review of protocols and reports. - Document management including BMRs, BPRs, master SOPs, etc. - Handling of change control, deviations, CAPA, investigations, etc. - Overseeing manufacturing, filling & sealing, labeling, and packing operations. - Production planning on a monthly and daily basis as per material availability. - Preparation of daily production reports. - Ensuring equipment and lines are validated and calibrated. - Adherence to cGMP, GDP, and department discipline. - Checking manufacturing, washing, filling, sealing, and sterilization records and log books. - Providing training to subordinates, technicians, and operators. - Undertaking additional activities as per the requirement of the HOD. You will also be expected to attend training sessions, maintain the facility in compliance, and ensure readiness for inspections. Qualifications required for this role include: - B.Pharma or M.Pharma degree. - Total experience of 15-18 years in sterile manufacturing plant. Should you be selected for this position, you will play a crucial role in maintaining the operational efficiency and quality standards of the sterile manufacturing department. As a candidate for the position, you will be responsible for various key activities in the sterile manufacturing department. Your job responsibilities will include: - Updating on self-hygiene. - Preparation, review, revision, control, and implementation of standard operating procedures. - Preparation and review of master production documents. - Preparation and review of protocols and reports. - Document management including BMRs, BPRs, master SOPs, etc. - Handling of change control, deviations, CAPA, investigations, etc. - Overseeing manufacturing, filling & sealing, labeling, and packing operations. - Production planning on a monthly and daily basis as per material availability. - Preparation of daily production reports. - Ensuring equipment and lines are validated and calibrated. - Adherence to cGMP, GDP, and department discipline. - Checking manufacturing, washing, filling, sealing, and sterilization records and log books. - Providing training to subordinates, technicians, and operators. - Undertaking additional activities as per the requirement of the HOD. You will also be expected to attend training sessions, maintain the facility in compliance, and ensure readiness for inspections. Qualifications required for this role include: - B.Pharma or M.Pharma degree. - Total experience of 15-18 years in sterile manufacturing plant. Should you be selected for this position, you will play a crucial role in maintaining the operational efficiency and quality standards of the sterile manufacturing department.

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Amneal Pharmaceuticals logo
Amneal Pharmaceuticals

Pharmaceutical Manufacturing

Bridgewater New Jersey

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