About Baxter
Baxter one of the top Pharmaceutical and medical devices company, with the head quarters located in Illinois. Primary focus of treatment for the company is in the area of Hemophilia and in treating the immune and chronic medical conditions. The firm relieves the issues for millions of patients across the globe serving to the man kind from more than 85 years.
In the year 2018 Baxter was awarded for the best place to work globally. The company have the portfolio of medicines in Critical care, Nutritional, renal care, surgical and Hospital care. Apart from the pharmaceutical medicines the company also provides medical devices and infusions.
About the Company :
Location : Ahmedabad
Experience : Required experience in Injectable vial filling and mixing activity with 2-5 years of experience
Qualification : Minimum of ITI is required
Roles / Responsibility
Needed to maintain the cleaning and lubrication of machine regularly and necessary to follow SOP and guide others also to follow the same.
To ensure the machine is working smoothly and it is performing well and further experience in settle plate under Filling LAF of Manufacturing Line as per defined frequency.
Knowledge in replacement of change parts and trial of machine within the time limit and review of preventive maintenance of machine is performed regularly and timely
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Maintenance of machine in good condition by regular cleaning and lubrication and cleaning and steaming process is carried out as per validated procedure.
Effective monitor the productivity continuously, if productivity is less than defined norms, take action immediately and highlighting the Technical Department regarding any kind of maintenance work of clean room through work request form and inform to Sub Department Manager.
Required to ensure proper gowning of personnel working in clean room.
Timely ensure follow up of Standard Operating Procedure (SOP) during entry / exit from clean room
Able to timely ensure cleanliness of airlocks after entry and exit of the workers and verify the equipment after preventive maintenance and if found any dissatisfaction; ensure not to start further process.
Record the volume data in specified intervals, and if any abnormality is found, rectify immediately and inform to Sub Department Manager and Quality Assurance (QA) Department.