Manager, Manufacturing Injectables

5 - 9 years

0 Lacs

Posted:2 weeks ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

As a candidate for this role, you will be responsible for the following key tasks: - Updating on self-hygiene. - Preparation, review, revision, control, and implementation of standard operating procedures of the sterile manufacturing department. - Preparation and review of Protocols and reports based on the requirements. - Document management including BMRs, BPRs, Master SOPs, etc. - Handling of Change Control, Deviations, CAPA, Investigation, etc. - Generating general purchase indent for departmental general items. - Preparation of production planning on a monthly and daily basis as per the requirement and availability of materials. - Preparation of a daily production report based on the production achieved. - Ensuring that all equipment and lines are in validated and calibrated status. - Following cGMP, GDP, and discipline in the department and ensuring all employees follow the same. - Providing training to all subordinates, technicians, and operators of the department. - Performing activities as per the requirement of HOD, by following instructions and guidance. - Attending training as per the schedule and ensuring training as per TNI. - Preparation and review of all master documents of production. - Ensuring cleaning, sanitization, and operation of machines as per Standard Operating Procedures. - Controlling aseptic area operations like sterilization, manufacturing, washing & dehydrogenation, filling, and sealing. - Performing line clearance activity before commencing operations like manufacturing, filling & sealing. Qualifications required for this role include: - M.Sc. / B.Pharm / M.Pharm Please note that this job description does not provide additional details about the company. As a candidate for this role, you will be responsible for the following key tasks: - Updating on self-hygiene. - Preparation, review, revision, control, and implementation of standard operating procedures of the sterile manufacturing department. - Preparation and review of Protocols and reports based on the requirements. - Document management including BMRs, BPRs, Master SOPs, etc. - Handling of Change Control, Deviations, CAPA, Investigation, etc. - Generating general purchase indent for departmental general items. - Preparation of production planning on a monthly and daily basis as per the requirement and availability of materials. - Preparation of a daily production report based on the production achieved. - Ensuring that all equipment and lines are in validated and calibrated status. - Following cGMP, GDP, and discipline in the department and ensuring all employees follow the same. - Providing training to all subordinates, technicians, and operators of the department. - Performing activities as per the requirement of HOD, by following instructions and guidance. - Attending training as per the schedule and ensuring training as per TNI. - Preparation and review of all master documents of production. - Ensuring cleaning, sanitization, and operation of machines as per Standard Operating Procedures. - Controlling aseptic area operations like sterilization, manufacturing, washing & dehydrogenation, filling, and sealing. - Performing line clearance activity before commencing operations like manufacturing, filling & sealing. Qualifications required for this role include: - M.Sc. / B.Pharm / M.Pharm Please note that this job description does not provide additional details about the company.

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Amneal Pharmaceuticals logo
Amneal Pharmaceuticals

Pharmaceutical Manufacturing

Bridgewater New Jersey

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