Assistant / Associate - Batch Manufacturing Amneal Pharmaceuticals

3.0 - 7.0 years

0 Lacs

ahmedabad, gujarat

On-site

As a Manufacturing Operator, you will be responsible for attending training sessions according to the schedule and ensuring that you apply the knowledge gained in Training Needs Identification (TNI). Your primary duties will include monitoring and performing all activities within the Manufacturing area, maintaining logs, Batch Manufacturing Records (BMRs), and other relevant documents as per Standard Operating Procedures (SOPs) and work instructions. Additionally, you will be in charge of adhering to the preventive maintenance schedule for machinery, instruments, and equipment in the manufacturing area, as well as overseeing their cleaning and sanitization. Line clearance activities before operations, Clean-in-Place (CIP), and Steam-in-Place (SIP) of Vessel operations will be under your responsibility. You will operate specific machinery such as the Manufacturing Vessel and CIP module. It is crucial that you promptly report any observations or disturbances in the aseptic area to the relevant supervisor. Maintaining personal hygiene, cleanliness, and following SOPs while documenting all activities within the area will be essential tasks. Furthermore, you must ensure that the Unit Area File (UAF) is up to date and operational within the designated area. Compliance with current Good Manufacturing Practices (cGMP), Good Documentation Practices, and maintaining discipline within the department are also key aspects of this role. Qualifications: - Qualification Requirement: ITI/ Diploma in Mechanical Engineering - Experience: 3-6 years - Skilled Operator needed for CIP & SIP of Vessel, Filter integrity checks, and Batch manufacturing activities - Prior experience in the aseptic area for Manufacturing Injectable Products is preferred If you meet the qualifications and possess the necessary skills, we encourage you to apply for this position and contribute to our manufacturing operations effectively.,

Posted 1 day ago

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Manager-Manufacturing Amneal Pharmaceuticals

2.0 - 6.0 years

0 Lacs

ahmedabad, gujarat

On-site

You will be responsible for performing line clearance activities before commencing operations, ensuring a clean and sanitized visual inspection and Packing area, and following the preventive maintenance schedule of machines. Operating the machines efficiently and filling the log of general areas as per SOP and work execution will also be part of your responsibilities. It is essential to adhere to cGMP, GDP, and maintain discipline in the department while ensuring that all employees comply with the same standards. Your role will involve ensuring that all equipment and production lines are in validated and calibrated status, preparing daily production reports based on achieved targets, and creating production plans on a monthly and daily basis according to material availability. Handling tasks such as change control, deviations, CAPA, investigations, and document management including BMRs, BPRs, and master SOPs will be part of your duties. You will also be involved in the preparation, review, revision, control, and implementation of standard operating procedures within the sterile manufacturing department. Conducting line clearance activities before commencing various operations such as manufacturing, sterilization, and filling, as well as checking and maintaining records and logbooks related to manufacturing processes, garment washing, drying, and equipment sterilization are key aspects of your role. Additionally, you will be required to perform any activities as instructed by the HOD, provide training to subordinates, technicians, and operators, and stay updated on self-hygiene practices. Attending training sessions as per the schedule and ensuring compliance with the Training Need Identification (TNI) will also be part of your responsibilities. Qualifications required for this role include M.Sc., B.Pharm, or M.Pharm degree.,

Posted 5 days ago

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