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We believe every person deserves a chance for a healthy life, free from illness and full of possibility. We see a world full of healing, with viable care options available to those with limited choices today. We envision new ways of providing physicians, pharmacists and nurses with technologies that not only treat chronic diseases, but also work to prevent them. We’re looking for team members who are motivated to learn, grow and innovate, while making a meaningful difference for millions of people around the world.

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To ensure the cleanliness of various areas like autoclave area, pre-sterilization area, post sterilization area, sterilizers and if any deviation is found, document and escalate the point, get it corrected immediately in coordination of production Sub-Department Manager and QA Sub-Department Manager as per defined SOP, and then start the further process.

To ensure cleaning and sterilization of disinfectant preparation and filtration requirements is done as per SOPs  To ensure that component(s) and product(s) are sterilized as per validated parameters. 

To ensure the availability of sterilized clean room garments and goggles. 

To supervise the behavior of workers at product loading & unloading site and during handling stages of sterilizer trolleys 

To check the online rejection(s), escalate and take immediate corrective action to minimize it in coordination of Production Manager and QA Manager. 

To ensure not to start the sterilization process if found any abnormality in sterilizer. Raise Work Request and ensure corrective and preventive actions are defined and implemented. 

To ensure not to start next cycle of Sterilization without rectification of problem, in case of any abnormality observed in printer, recorder, temperature, pressure and utility supply during the sterilization of any product. 

To check the equipment after preventive maintenance and if found any abnormality; ensure not to start further process. 

To record all the activities in the approved formats at the time of observation/activity is performed. 

To have thorough knowledge of SOP of own working area and ensure to practice it. 

To follow clean room behaviors strictly. 

Ensure that the PM, calibration and validation of equipment/system/facility is completed as per approved schedule. 

Ensure the housekeeping of the area is in controlled state. 

Ensure all safety norms are followed in respective area. 

Keep self and team updated about CGMP requirement. 

Ensure completion of all required training for self as well as team.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
                                                                                                                                                               
EEO is the Law 
EEO is the law - Poster Supplement 
Pay Transparency Policy

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to Americas_TTA@baxter.com and let us know the nature of your request along with your contact information.