This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride.
Requirements:
To ensure cleanliness and environmental norms of various area like filling including air locks
To ensure availability of clean room garments and goggles
To inform supervisor if any abnormality observed in on going batch
To perform the verification activity during manufacturing operation. (i.e., Cleaning /manufacturing verification)
To ensure that all activities carried out in compliance mode
To implement cGMP norms on a continuous basis in the production area
To check and verify the equipment after preventive maintenance. If any abnormality found, rectify it for smooth operation
To follow SOP and ensure that workers are also adhered to Standard Operating Procedure
To ensure the status tags are displayed properly so that the status of each issued & filled container is maintained as per the regulatory requirement and Standard Operating Procedure
To ensure that status label is being updated to avoid mix-up of goods container & rejected container
To adhere with process of reconciliation of material after completion of batch
To co-ordinate with engineering department for the plant related repair and preventive maintenance and EMS/BMS excursion
To perform filling related in process check in specified intervals, and if any abnormality is found, rectify immediately in line with Standard Operating Procedure and inform to supervisor and Quality Assurance (QA) Department
To adhere with current Good Manufacturing Practice (cGMP), Good Document Practice (GDP), Standard Operating procedure (SOP) & Data Integrity Principles i.e., Attributable, Legible, Contemporaneous, Original and Accurate (ALCOA+)
To ensure availability of Batch manufacturing Record (BMR) for execution as per plan & submission of executed BMR
To ensure availability of sterilized component as per filling operation plan of manufacturing line
To communicate with chemist and supervisor for production activity/ plan, rejection and break down
To ensure wearing the PPEs while working in routine operation/maintenance of any machine as per requirements
To inform supervisor regarding a safety/ Hazard concern in area
To perform/ ensure lockout-tagout procedure for critical equipment, valves, utility against unintentional exposure to hazards
To communicate for any utility or technical problems to concern department to avoid the production loss or any quality issue
To stop the activity if any non-conformance found in activity and inform to superior
In absence of operator, chemist will ensure roles and responsibility