Sr Executive, Production - Sterilization Job in Baxter

Are you looking for a career that matters?

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. Were looking for team members who are motivated to learn, grow and innovate, while making a meaningful difference for millions of people around the world.

Learn more about how Baxter is .

Major Roles & Responsibilities:

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.

Skills Required- Functional/Behavioural

Knowledge about the working /design principles equipment, system, facility utilized for injectable manufacturing.

Knowledge about documentation requirements as per current regulatory norms and best industry practices.

Exposure to international regulatory audits.

Computer literacy.

Good verbal and written communication skills.

Self-motivated and result oriented.

Leadership quality.

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 [email protected] and let us know the nature of your request along with your contact information.