Baxter Pharma Production Executive Recruitment - Apply Online

Baxter Pharma Production Executive Vacancy – Apply Online

Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, they create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join them at the intersection of saving and sustaining lives—where your purpose accelerates our mission.

Job Title: Sr. Executive, Production

Req # JR – 040756

Location Ahmedabad, Gujarat, India

Job Category Manufacturing

Qualification & Experience-

Diploma/ B. Pharma/ B.sc/ M.sc/BE with experience of 2 to 6 years from injectable production sterilization of disinfectant activity.

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

  • 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 the 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 cleanroom 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 the coordination of Production Manager and QA Manager.
  • To ensure not to start the sterilization process if found any abnormality in the sterilizer. Raise Work Requests and ensure corrective and preventive actions are defined and implemented.
  • To ensure not to start next cycle of Sterilization without rectification of the 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 the further process.
  • To record all the activities in the approved formats at the time of observation/activity is performed.
  • To have a 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 the approved schedule.
  • Ensure the housekeeping of the area is in a controlled state.
  • Ensure all safety norms are followed in the respective areas.
  • Keep self and team updated about CGMP requirements.
  • Ensure completion of all required training for self as well as a team.

Apply Online

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